2018 Edition of The European Association of Urology (EAU) Guidelines

European
Association
of Urology
Pocket Guidelines
2018 edition
Introduction
We are pleased to present the 2018 edition of the European
Association of Urology (EAU) Guidelines. The EAU Guidelines
are the most comprehensive, continuously updated,
guidelines available for urologists and related specialties.
Produced by a dedicated Guidelines Office, involving
approximately 300 international experts drawn from across
Europe and beyond, the EAU Guidelines are internationally
recognised as an excellent, high-quality, resource for assisting
clinicians in their everyday practice.
Clinical guidelines are a highly influential tool for improving

clinical care, unifying healthcare provision and managing
healthcare-associated resources across Europe and beyond.
Consequently, they must be transparent, free of bias, give a
balanced account of risks and benefits and take into
consideration patient preferences. To this end, the 2018
guidelines sees the implementation of a new system for
grading guidelines recommendations based upon a
modified GRADE (Grading of Recommendations Assessment,
Development and Evaluation) approach. Consequently, each
and every recommendation contained within the guidelines,
along with the evidence underpinning it, has been reassessed
and a Strength Rating Form produced (posted online at:
www.uroweb.org/guidelines). Recommendations now take
into account the available evidence, the strength and overall
quality of that evidence, the balance between desirable and
undesirable consequences of any given recommendation
compared with alternative interventions, whilst also taking
into account patients’ values and preferences. A further
change can also be found in the way in which the strength of
Introduction 1
each recommendation is represented. Recommendations are
no longer denoted by alphabetic characters, but rather by the
words ‘strong’ or ‘weak’, with each panel providing both ‘strong’
and ‘weak’ recommendations ‘for’ or ‘against’ a specific
intervention. We hope that you find the new format useful and
that they provide helpful, clear and unambiguous guidance.
Going forward, a key aim of the EAU Guidelines office is to

increase patient involvement in Guidelines development.
The ultimate aim of this project being the establishment of
an effective framework that can ensure that the voices of
patients are captured in the development of future guidelines
recommendations. The EAU Guidelines Office believes that
structured patient engagement will result in
recommendations that lead to better treatment compliance
and improved health outcomes. This promises to be a
challenging but a worthwhile long-term endeavour.
The annual publication of the EAU Guidelines would not

be possible without the steadfast support of every user of
the Guidelines globally, our EAU membership, our greatly
respected Guidelines Panels, Guidelines Associates, the EAU
Executive Committee and Management team and, last but not
least, the National Societies. So, on behalf of the EAU Guidelines
Office Board, thank you for your support and inspiration.
We hope you find the 2018 update of the EAU Guidelines a

pleasure to use!
Prof. James N’Dow

Chairman EAU Guidelines Office
2 Introduction
Board Members EAU Guidelines Office:
Prof.Dr. J. N’Dow, Aberdeen (UK) (chair)
Prof.Dr. A. Bjartell, Malmö (SE)
Prof.Dr. A. Briganti, Milan (IT)
Mr. P. Cornford, Liverpool (UK)
Prof.Dr. T. Knoll, Sindelfingen (DE)
Prof.Dr. M.J. Ribal, Barcelona (ES)
Prof.Dr. R. Sylvester, Brussels (BE)
Prof.Dr. T. Loch, Flensburg (DE) (ex-officio)
Prof.Dr. H. Van Poppel, Leuven (BE) (ex-officio)
Level of evidence and grading systems

The EAU Guidelines Office have transitioned to a modified
GRADE methodology for the 2018 EAU Pocket Guidelines [1, 2].
Each recommendation within the 2018 Pocket Guidelines
is accompanied by an online strength rating form which
addresses a number of key elements, namely:
1. t he overall quality of the evidence which exists for the

recommendation, references used in this text are graded
according to a classification system modified from the
Oxford Centre for Evidence-Based Medicine Levels of
Evidence (see Table 1) [3];
2. the magnitude of the effect (individual or combined
effects);
3. t he certainty of the results (precision, consistency,
heterogeneity and other statistical or study related
factors);
4. the balance between desirable and undesirable
outcomes;
Introduction 3
5. the impact of patient values and preferences on the
intervention;
6. t he certainty of those patient values and preferences.
These key elements are the basis which panels use to define
the strength rating of each recommendation. The strength of
each recommendation is represented by the words ‘strong’
or ‘weak’ [4]. The strength of each recommendation is
determined by the balance between desirable and
undesirable consequences of alternative management
strategies, the quality of the evidence (including certainty of
estimates), and nature and variability of patient values and
preferences. The strength rating forms will be available online.
Table 1: Level of evidence*
LevelType of evidence
1a Evidence obtained from meta-analysis of randomised
trials.
1b Evidence obtained from at least one randomised
trial.
2a Evidence obtained from one well-designed
controlled study without randomization.
2b Evidence obtained from at least one other type of
well-designed quasi-experimental study.
3 Evidence obtained from well-designed non-
experimental studies, such as comparative studies,
correlation studies and case reports.
4 Evidence obtained from expert committee reports
or opinions or clinical experience of respected
authorities.
* Modified from [3]
4 Introduction
References
1. Guyatt, G.H., et al. GRADE: an emerging consensus on rating quality of evidence
and strength of recommendations. BMJ, 2008. 336: 924.
2. Guyatt, G.H., et al. What is “quality of evidence” and why is it important to
clinicians? BMJ, 2008. 336: 995.
3. Phillips, B., et al. Oxford Centre for Evidence-based Medicine Levels of Evidence.
Updated by Jeremy Howick March 2009.
4. Guyatt, G.H., et al. Going from evidence to recommendations. BMJ, 2008. 336:
1049.
Introduction 5
6 Introduction
Page 9 Non-muscle Invasive Bladder Cancer
Page 27 Urothelial Carcinoma of the Upper Urinary Tract
Page 37 Muscle-invasive and Metastatic Bladder Cancer
Page 53 Prostate Cancer
Page 79 Renal Cell Carcinoma
Page 101 Testicular Cancer
Page 120 Penile Cancer

Page 135 Non-neurogenic Male LUTS,
incl. benign prostatic obstruction (BPO)
Page 155 Urinary Incontinence
Page 179 Neuro-Urology

Page 192 Male Sexual Dysfunction:
Erectile Dysfunction and Premature Ejaculation
Page 208 Priapism
Page 217 Penile Curvature
Page 225 Male Infertility
Page 242 Male Hypogonadism
Page 253 Urological Infections
Page 273 Urolithiasis
Page 306 Paediatric Urology
Page 338 Urological Trauma
Page 355 Chronic Pelvic Pain
Page 378 Renal Transplantation
Page 398 Thromboprophylaxis in Urological Surgery
7
8
EAU GUIDELINES ON
NON-MUSCLE-INVASIVE (TaT1, CIS)
BLADDER CANCER
(Limited text update March 2018)
M. Babjuk (Chair), M. Burger (Vice-chair), E. Compérat,

P. Gontero, A.H. Mostafid, J. Palou, B.W.G. van Rhijn, M. Rouprêt,
S.F. Shariat, R. Sylvester, R. Zigeuner
Guidelines Associates: O. Capoun, D. Cohen, V. Hernández,
V. Soukup
Introduction
The EAU Working Group has published guidelines on
Non-muscle-invasive bladder cancer (NMIBC), TaT1 tumours
and carcinoma in situ (CIS).
Staging and classification systems

The 2017 TNM (Tumour, Node, Metastasis Classification) is
used for staging (Table 1). For grading, both the 1973 and 2004
WHO Grading classifications are used (Table 2).
Non-muscle-invasive (TaT1, CIS) Bladder Cancer 9

Table 1: TNM Classification 2017
T - Primary Tumour
TX Primary tumour cannot be assessed
T0 No evidence of primary tumour
Ta Non-invasive papillary carcinoma
Tis Carcinoma in situ: ’flat tumour’
T1 Tumour invades subepithelial connective tissue
T2 Tumour invades muscle
T2a Tumour invades superficial muscle (inner half)
T2b Tumour invades deep muscle (outer half)
T3 Tumour invades perivesical tissue
T3a Microscopically
T3b Macroscopically (extravesical mass)
T4 Tumour invades any of the following: prostate stroma,
seminal vesicles, uterus, vagina, pelvic wall, abdominal
wall
T4a Tumour invades prostate stroma, seminal
vesicles, uterus or vagina
T4b Tumour invades pelvic wall or abdominal wall
N – Regional Lymph Nodes
NX Regional lymph nodes cannot be assessed
N0 No regional lymph node metastasis
N1 Metastasis in a single lymph node in the true pelvis
(hypogastric, obturator, external iliac, or presacral)
N2 Metastasis in multiple regional lymph nodes in the
true pelvis (hypogastric, obturator, external iliac, or
presacral)
N3 Metastasis in common iliac lymph node(s)
10 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

M - Distant Metastasis
M0 No distant metastasis
M1a Non-regional lymph nodes
M1b Other distant metastases
The prognostic value of both WHO 1973 and 2004 grading

systems has been confirmed. The WHO 2004 system has not
yet been fully incorporated into prognostic models.
Carcinoma in situ
Carcinoma in situ (CIS) is a flat, high-grade, non-invasive
urothelial carcinoma, and classified into the following clinical
types:
• Primary: isolated CIS with no previous or concurrent
papillary tumours and no previous CIS;
• Secondary: CIS detected during follow-up of patients with
a previous tumour that was not CIS;
• Concurrent: CIS in the presence of any other urothelial
tumour in the bladder.
Table 2: WHO grading in 1973 and in 2004
1973 WHO grading

Grade 1: well differentiated
Grade 2: moderately differentiated
Grade 3: poorly differentiated
2004 WHO grading system (Papillary lesions)

Papillary urothelial neoplasm of low malignant potential
(PUNLMP)
Low-grade (LG) papillary urothelial carcinoma
High-grade (HG) papillary urothelial carcinoma

Recommendations for bladder cancer Strength rating
classification (NMIBC)
Use the 2017 TNM system for classification Strong
of the depth of tumour invasion (staging).
Use both the 1973 and 2004/2016 WHO Strong
grading systems for histological
classification.
Do not use the term “superficial bladder Strong
cancer”.
Mention the tumour stage and grade Strong
whenever the terminology NMIBC is used
in individual cases.
Diagnosis
A comprehensive patient history is mandatory. Haematuria
is the most common finding. Physical examination does not
reveal NMIBC.
Recommendations for the primary Strength rating

assessment of non-muscle-invasive
bladder cancer (NMIBC)
Take a patient history, focusing on urinary Strong
tract symptoms and haematuria.
Renal and bladder ultrasound and/or Weak
computed tomography-intravenous
urography may be used during the initial
work-up in patients with haematuria.
Once a NMIBC has been detected, perform Strong
a computed tomography urography in
selected cases (e.g., tumours located in the
trigone, multiple- or high-risk tumours).

Perform cystoscopy in patients with Strong
symptoms suggestive of bladder cancer or
during surveillance. It cannot be replaced by
cytology or by any other non-invasive test.
In men, use a flexible cystoscope, if available. Strong
Describe all macroscopic features of the Strong
tumour (site, size, number and appearance)
and mucosal abnormalities during
cystoscopy. Use a bladder diagram.
Use voided urine cytology as an adjunct to Strong
cystoscopy to detect high-grade tumour.
Perform cytology on fresh urine or urine Strong
with adequate fixation. Morning urine is not
suitable because of the frequent presence
of cytolysis.
Use the Paris system for cytology reporting. Strong
Repeat urine cytology in patients with Weak
initial cytology results suspicious for
high-grade urothelial carcinoma.
Papillary (TaT1) tumours

The diagnosis of papillary bladder cancer ultimately depends
on cystoscopic examination of the bladder and histological
evaluation of the tissue resected during transurethral
resection (TURB). TURB is a crucial procedure in the diagnosis
and treatment of TaT1 tumours and should be performed
systematically in individual steps (see recommendations
below). The strategy of resection depends on the size of the
lesion. In selected cases, due to the risk of tumour persistence
and understaging after initial TURB, a second resection
(2nd TURB) is recommended.

Carcinoma in situ
Carcinoma in situ is diagnosed by a combination of
cystoscopy, urine cytology, and histological evaluation of
multiple bladder biopsies. Carcinoma in situ cannot be
eradicated by TURB and further treatment is mandatory.
Recommendations for transurethral Strength rating

resection of the bladder (TURB), biopsies
and pathology report
In patients suspected of having bladder Strong
cancer, perform a TURB followed by
pathology investigation of the obtained
specimen(s) as a diagnostic procedure and
initial treatment step.
Perform TURB systematically in individual Strong
steps:
• bimanual palpation under anaesthesia;
• insertion of the resectoscope, under
visual control with inspection of the
whole urethra;
• inspection of the whole urothelial lining
of the bladder;
• biopsy from the prostatic urethra
(if indicated);
• cold-cup bladder biopsies (if indicated);
• resection of the tumour;
• recording of findings in the surgery
report/record;
• precise description of the specimen for
pathology evaluation.

Performance of individual steps
Perform en-bloc resection or resection in Strong
fractions (exophytic part of the tumour, the
underlying bladder wall and the edges of
the resection area). The presence of
detrusor muscle in the specimen is
required in all cases except for TaG1/LG
tumours.
Avoid cauterisation as much as possible Strong
during TURB to avoid tissue deterioration.
Take biopsies from abnormal-looking Strong
urothelium. Biopsies from normal-looking
mucosa (trigone, bladder dome, and right,
left, anterior and posterior bladder wall) are
recommended when cytology is positive
or when high-risk exophytic tumour is
expected (non-papillary appearance). If
equipment is available, perform
fluorescence-guided (PDD) biopsies.
Take biopsy of the prostatic urethra in Strong
cases of bladder neck tumour, when
bladder carcinoma in situ is present or
suspected, when there is positive cytology
without evidence of tumour in the bladder,
or when abnormalities of the prostatic
urethra are visible. If biopsy is not
performed during the initial procedure, it
should be completed at the time of the
second resection.

Take the biopsy from abnormal areas in the Weak
prostatic urethra and from the precollicular
area (between the 5 and 7 o’ clock position)
using a resection loop. In primary non-
muscle-invasive tumours when stromal
invasion is not suspected, cold-cup biopsy
with forceps can be used.
Use methods to improve tumour Weak
visualisation (FC, NBI) during TURB, if
available.
Refer the specimens from different biopsies Weak
and resection fractions to the pathologist
in separately labelled containers.
The TURB protocol must describe tumour Strong
appearance, all steps of the procedure, as
well as the extent and completeness of
resection.
In patients with positive cytology, but Strong
negative cystoscopy, exclude an upper tract
urothelial carcinoma, CIS in the bladder
(random biopsies or PDD-guided biopsies)
and tumour in the prostatic urethra
(prostatic urethra biopsy).
Perform a second TURB in the following Strong
situations:
• after incomplete initial TURB, or in
case of doubt about completeness of a
TURB);
• if there is no muscle in the specimen
after initial resection, with the exception
of TaLG/G1 tumours and primary CIS;
• in T1 tumours.

If indicated, perform a second TURB within Weak
two to six weeks after initial resection. This
second TURB should include resection of
the primary tumour site.
Register the pathology results of a second Weak
TURB as it reflects the quality of the initial
resection.
Inform the pathologist of prior treatments Strong
(intravesical therapy, radiotherapy, etc.).
Pathological report
The pathological report should specify Strong
tumour location, tumour grade, depth of
tumour invasion, presence of CIS, and
whether the detrusor muscle is present in
the specimen.
The pathological report should specify the Strong
presence of lymphovascular invasion or
unusual (variant) histology.
Predicting disease recurrence and progression

After TURB, patients should be stratified, according to
prognostic factors, into risk groups which will facilitate
treatment recommendations (see Table 3). For individual
prediction of the risk of tumour recurrence and progression at
different intervals after TURB, application of EORTC risk tables
and calculator (http://www.eortc.be/tools/bladdercalculator/)
is strongly recommended.
For bacillus Calmette-Guerin (BCG)-treated patients,
scoring models have been created by the CUETO and the
EORTC. The CUETO risk calculator is available at: http://www.
aeu.es/Cueto.html.

Table 3: Treatment recommendations in TaT1 tumours and
carcinoma in situ according to risk stratification
Risk category Definition Treatment

recommendation
Low-risk Primary, solitary, One immediate
tumours TaG1 (PUNLMP, instillation of intra-
LG*), < 3 cm, no vesical chemotherapy
CIS. after TURB.
Intermediate- All tumours not In patients with
risk tumours defined in the previous low
two adjacent recurrence rate (≤ one
categories recurrence per year)
(between the and expected EORTC
category of low recurrence score < 5,
and high-risk). one immediate
instillation of
intravesical
chemotherapy after
TURB. In all patients
either one-year full-
dose BCG treatment
(induction plus three-
weekly instillations at
three, six and twelve
months), or instillations
of chemotherapy (the
optimal schedule is not
known) for a maximum
of one year.

High-risk Any of the Intravesical full-dose
tumours following: BCG instillations for
• T1 tumours; one to three years or
• G3 (HG**) tumour; radical cystectomy (in
• CIS; highest-risk tumours -
• Multiple, see below).
recurrent and
large (> 3 cm)
TaG1G2/LG
tumours (all
features must be
present)*.
Subgroup of highest-risk tumours

T1G3/HG Radical cystectomy (RC)
associated with should be considered.
concurrent bladder
CIS, multiple and/ In those who refuse
or largeT1G3/HG or are unfit for RC
and/or recurrent intravesical full-dose
T1G3/HG, T1G3/HG BCG instillations for
with CIS in the one to three years.
prostatic urethra,
some forms of
variant histology
of urothelial
carcinoma, LVI.
BCG-refractory Radical cystectomy is
tumours. recommended.
*Low grade is a mixture of G1 and G2.

** High grade is a mixture of some G2 and all G3.

Recommendations for stratification of Strength rating
non-muscle-invasive bladder cancer
Stratify patients into three risk groups Strong
according to Table 3.
Apply the EORTC risk tables and calculator Strong
for the prediction of the risk of tumour
recurrence and progression in different
intervals after transurethral resection of
the bladder, in individual patients.
Use the CUETO risk tables and the new Strong
EORTC risk groups for the prediction of the
risk of tumour recurrence and progression
in individual patients treated with bacillus
Calmette-Guérin.
Disease management
Adjuvant treatment
Since there is considerable risk for recurrence and/or
progression of tumours after TURB, adjuvant intravesical
therapy is recommended for all stages (TaT1, and CIS).
• Immediate single post-operative instillation of chemo-
therapy within six hours after TURB can reduce recurrence
rate in patients with low-risk and selected intermediate-
risk tumours. The difference of efficacy between individual
drugs (mitomycin C, epirubicin, or doxorubicin) has not
been confirmed.
• Further chemotherapy instillations can improve
recurrence-free survival in intermediate-risk tumours,
but do not prevent progression. These instillations are
associated with minor side-effects.
• Intravesical immunotherapy with BCG (induction and
maintenance) is superior to intravesical chemotherapy
in reducing recurrences and in preventing or delaying
progression to muscle-invasive bladder cancer. However,
intravesical BCG is more toxic.

The individual choice of further intravesical adjuvant therapy
depends on the patient’s risk (Table 3). In patients at highest
risk of progression, radical cystectomy (RC) should be
considered. Patients with BCG failure are unlikely to respond
to further BCG therapy; RC is therefore the preferred option.
General recommendations for adjuvant Strength rating

therapy in TaT1 tumours and for therapy
of CIS
Counsel smokers with confirmed non- Strong
muscle-invasive bladder cancer to stop
smoking.
The type of further therapy after Strong
transurethral resection of the bladder
should be based on the risk groups shown
in Table 3.
In patients with tumours presumed to be Strong
at low risk and in those presumed to be at
intermediate risk with previous low
recurrence rate (≤ one recurrence per year)
and expected EORTC recurrence score < 5,
one immediate chemotherapy instillation is
recommended.

In patients with intermediate-risk tumours Strong
(with or without immediate instillation),
one-year full-dose bacillus Calmette-
Guérin (BCG) treatment (induction plus
three-weekly instillations at 3, 6 and 12
months), or instillations of chemotherapy
(the optimal schedule is not known) for a
maximum of one year is recommended. The
final choice should reflect the individual
patient’s risk of recurrence and progression
as well as the efficacy and side effects of
each treatment modality.
In patients with high-risk tumours, full-dose Strong
intravesical BCG for one to three years
(induction plus three-weekly instillations
at 3, 6, 12, 18, 24, 30 and 36 months), is
indicated. The additional beneficial effect
of the second and third years of
maintenance should be weighed against
its added costs and inconveniences.
Offer transurethral resection of the Weak
prostate, followed by intravesical instillation
of BCG to patients with CIS in the epithelial
lining of the prostatic urethra.
Discuss immediate radical cystectomy (RC) Strong
with patients at highest risk of tumour
progression.
Perform a RC in patients with BCG failure. Strong
In patients with BCG-refractory tumours, Weak
who are not candidates for RC due to
comorbidities, use preservation strategies
(intravesical chemotherapy, chemotherapy
and microwave-induced hyperthermia).

Recommendations – technical aspects for treatment
Intravesical chemotherapy
If given, administer a single immediate Weak
instillation of chemotherapy within
24 hours after TURB.
Omit a single immediate instillation of Strong
chemotherapy in any case of overt or
suspected bladder perforation or bleeding
requiring bladder irrigation.
Give clear instructions to the nursing staff Strong
to control the free flow of the bladder
catheter at the end of the immediate
instillation.
The optimal schedule and duration of Weak
further intravesical chemotherapy
instillation is not defined; however, it
should not exceed one year.
If intravesical chemotherapy is given, it is Strong
advised to use the drug at its optimal pH
and to maintain the concentration of the
drug by reducing fluid intake before and
during instillation.
The length of individual instillation should Weak
be one to two hours.
BCG intravesical immunotherapy
Absolute contraindications of BCG Strong
intravesical instillation are:
• during the first two weeks after TURB;
• in patients with visible haematuria;
• after traumatic catheterisation;
• in patients with symptomatic urinary
tract infection.

Follow-up
As a result of the risk of recurrence and progression, patients
with NMIBC need to be followed-up. However, the frequency
and duration of cystoscopy and imaging should reflect the
individual patient’s degree of risk.
When planning the follow-up schedule and methods, the

following aspects should be considered:
• The prompt detection of muscle-invasive and HG/G3
non-muscle-invasive recurrence is crucial because a delay
in diagnosis and therapy can be life-threatening.
• Tumour recurrence in the low-risk group is nearly always
low stage and LG/G1. Small, TaLG/G1 papillary recurrence
does not present an immediate danger to the patient and
early detection is not essential for successful therapy.
Fulguration of small papillary recurrences on an outpatient
basis could be a safe option that reduces the therapeutic
burden. Multiple authors have even suggested temporary
surveillance in selected cases.
• The first cystoscopy after TURB at three months is a very
important prognostic indicator for recurrence and
progression. Therefore, the first cystoscopy should always
be performed three months after TURB in all patients with
TaT1 tumours and CIS.
• In tumours at low risk, the risk of recurrence after five
recurrence-free years is low.
• Discontinuation of cystoscopy or its replacement with less
invasive methods can be considered.
• In tumours originally intermediate- or high risk, recurrences
after ten years tumour-free are not unusual. Therefore,
life-long follow-up is recommended.
• The follow-up strategy must reflect the risk of extravesical
recurrence (prostatic urethra in men and upper urinary
tract in both genders).

• The risk of upper urinary tract recurrence increases in
patients with multiple- and high-risk tumours.
• Positive urine test results have a positive impact on the
quality of performed follow-up cystoscopy, supporting the
adjunctive role of urine tests during follow-up.
• In patients initially diagnosed with TaLG/G1-2 BC, US of the
bladder may be a mode of surveillance in case cystoscopy
is not possible or refused by the patient.
Recommendations for follow-up in Strength rating

patients after transurethral resection of
the bladder
Base follow-up of TaT1 tumours and Strong
carcinoma in situ (CIS) on regular
cystoscopy.
Patients with low-risk Ta tumours should Weak
undergo cystoscopy at three months. If
negative, subsequent cystoscopy is advised
nine months later, and then yearly for five
years.
Patients with high-risk tumours should Weak
undergo cystoscopy and urinary cytology
at three months. If negative, subsequent
cystoscopy and cytology should be
repeated every three months for a period of
two years, and every six months thereafter
until five years, and then yearly.
Patients with intermediate-risk Ta tumours Weak
should have an in-between (individualised)
follow-up scheme using cystoscopy.
Regular (yearly) upper tract imaging Weak
(computed tomography-intravenous
urography [CT-IVU] or IVU) is recommended
for high-risk tumours.

Endoscopy under anaesthesia and bladder Strong
biopsies should be performed when office
cystoscopy shows suspicious findings or if
urinary cytology is positive.
Consider random (R)-biopsies or Weak
photodynamic diagnosis (PDD)-guided
biopsies after intravesical treatment (at
three or six months) in patients with CIS.
During follow-up in patients with positive Strong
cytology and no visible tumour in the
bladder, R-biopsies or PDD-guided biopsies
(if equipment is available) and investigation
of extravesical locations (CT urography,
prostatic urethra biopsy) are recommended.
In patients initially diagnosed with TaLG/ Weak
G1-2 bladder cancer, use ultrasound of
the bladder during surveillance in case
cystoscopy is not possible or refused by
the patient.
This short booklet text is based on the more comprehensive

EAU Guidelines (ISBN: 978-94-92671-01-1), available to all members of
the European Association of Urology at their website:
http://www.uroweb.org/guidelines/.

EAU GUIDELINES ON UROTHELIAL
CARCINOMA OF THE UPPER URINARY
TRACT (UTUCs)
M. Rouprêt, M. Babjuk, M. Burger, E. Compérat, N.C. Cowan,

P. Gontero, A.H. Mostafid, J. Palou, B.W.G. van Rhijn,
S.F. Shariat, R. Sylvester, R. Zigeuner
Guidelines Associates: J.L. Dominguez-Escrig, B. Peyronnet,
T. Seisen
Epidemiology
UTUC are uncommon and account for only 5-10% of urothe-
lial cell carcinomas (UCs). They have a similar morphology
to bladder carcinomas and nearly all UTUCs are urothelial in
origin.
Staging and grading systems

The UICC 2017 TNM (Tumour, Node, Metastasis Classification)
for renal pelvis and ureter is used for staging (Table 1).
Tumour grade
There are currently two main classifications used for UTUC;
the 1973 WHO classification, which classifies tumours into
three grades, G1, G2 and G3, and the 2004 WHO classification,
which classifies tumours into three groups:
• papillary urothelial neoplasia of low malignant potential;
• low-grade carcinomas;
• high-grade carcinomas.
Upper urinary tract tumours with low malignant potential are

very rare.
Urothelial Carcinomas of the Upper Urinary Tract 27

T - Primary tumour
Tis Carcinoma in situ
T2 Tumour invades muscularis
T3 (Renal pelvis) Tumour invades beyond muscularis
into peripelvic fat or renal parenchyma
(Ureter) Tumour invades beyond muscularis into
periureteric fat
T4 Tumour invades adjacent organs or through the
kidney into perinephric fat
N - Regional lymph nodes
N1 Metastasis in a single lymph node 2 cm or less in
greatest dimension
N2 Metastasis in a single lymph node more than 2 cm or
multiple lymph nodes
M - Distant metastasis
M1 Distant metastasis
28 Urothelial Carcinomas of the Upper Urinary Tract

Diagnosis
UTUCs are diagnosed using imaging, cystoscopy, urinary
cytology and diagnostic ureteroscopy. The benefits of uretero-
scopy for pre-operative assessment should also be discussed
with the patient.
Recommendations Strength rating

Perform a cystoscopy to rule out Strong
concomitant bladder tumour.
Perform a computed tomography Strong
urography for upper tract evaluation and
for staging.
Use diagnostic ureteroscopy and biopsy Strong
only in cases where additional information
will impact treatment decisions.
Prognosis
UTUC invading the muscle wall usually has a very poor
prognosis. The main prognostic factors are listed in Figure 1.

Figure 1: UTUCs - Prognostic factors
UTUC
Systemac screening during medical interview
Suspicion of hereditary UTUC (10-20%) Sporadic UTUC

- Age < 60 yr (80-90%)
- Personal history of HNPCC-spectrum cancer
or
- First-degree relave < 50 yr with HNPCC-spectrum cancer
or
- Two first-degree relaves with HNPCC-spectrum cancer
Germ-line DNA sequencing: mutaon?
- Clinical evaluaon for other HNPCC-related cancer:

colorectal, gastrointesnal, endometrial ovarian and skin
- Close monitoring and follow-up
- Familial genec counselling
ASA = American Society of Anesthesiologists; BMI = body

mass index; ECOG PS = Eastern Cooperative Oncology Group
performance status performance score.
Risk stratification
It is necessary to ‘risk-stratify’ UTUC cases before treatment to
identify those patients (and tumours) who are more suitable
for kidney-sparing management rather than radical extirpative
surgery (Figure 2).

Figure 2: Pre-intervention risk stratification of UTUCs
UTUC
Low-risk UTUC* High-risk UTUC**
• Unifocal disease • Hydronephrosis

• Tumour size < 2 cm • Tumour size > 2 cm
• Low-grade cytology • High-grade cytology
• Low-grade URS biopsy • High-grade URS biopsy
• No invasive aspect on CT-urography • Mulfocal disease
• Previous radical cystectomy for
bladder cancer
• Variant histology
*All of these factors need to be present.

** Any of these factors need to be present.
CTU = computed tomography urography;
URS = ureterorenoscopy.
Disease management (see also Figures 3 & 4)

Localised disease
Kidney-sparing surgery
Kidney-sparing surgery for low-risk UTUC consists of surgery
preserving the upper urinary renal unit. It is used in imperative
cases (renal insufficiency, solitary functional kidney). Kidney-
sparing surgery can also be considered in select patients with
serious renal insufficiency or solitary kidney.
Kidney-sparing surgery in low-risk UTUCs potentially allows
avoiding the morbidity associated with open radical surgery
without compromising oncological outcomes and kidney
function.

Offer kidney-sparing management as Strong
primary treatment option to patients with
low-risk tumours.
Offer a kidney-sparing management to Weak
patients with high-risk distal ureteral
tumours.
Offer kidney-sparing management to Strong
patients with solitary kidney and/or
impaired renal function, providing that it
will not compromise survival. This decision
will have to be made on a case-by-case
basis with the patient.
Use a laser for endoscopic treatment of Weak
upper tract urothelial carcinoma.
The instillation of bacillus Calmette-Guérin or mitomycin C

in the urinary tract by percutaneous nephrostomy or via a
ureteric stent is technically feasible after kidney-sparing
management or for treatment of carcinoma in situ. However,
the benefits have not been confirmed.
Radical nephroureterectomy
Open RNU with bladder cuff excision is the standard treat-
ment for high-risk UTUC, regardless of tumour location.

Perform radical nephroureterectomy in Strong
patients with high-risk tumours.
Technical steps of radical nephroureterectomy:
Remove the bladder cuff. Strong
Perform a lymphadenectomy in patients Weak
with high-risk tumours.
Offer a post-operative bladder instillation Strong
of chemotherapy to lower the intravesical
recurrence rate.
Advanced disease
Radical nephroureterectomy (RNU) has no benefit in
metastatic (M+) disease, but may be used in palliative care. As
UTUC are urothelial tumours, platinum-based chemotherapy
should give similar results to those in bladder cancer.
Currently, insufficient data are available to provide any
recommendations.
Radiotherapy is no longer relevant nowadays, not as a sole
treatment option, nor as an adjunct to chemotherapy.
Follow-up after initial treatment

In all cases, there should be strict follow-up after radical
management to detect metachronous bladder tumours,
as well as invasive tumours, local recurrence and distant
metastases. When kidney-sparing surgery is performed, the
ipsilateral upper urinary tract requires careful follow-up due
to the high risk of recurrence.

After radical nephroureterectomy:
Low-risk tumours
Perform cystoscopy at three months. If Weak
negative, perform subsequent cystoscopy
nine months later and then yearly, for five
years.
Perform computed tomography urography Weak
every year, for five years.
High-risk tumours
Perform cystoscopy and urinary cytology Weak
at three months. If negative, repeat
subsequent cystoscopy and cytology every
three months for a period of two years, and
every six months thereafter until five years,
and then yearly.
Perform computed tomography urography Weak
every six months for two years, and then
yearly.
After kidney-sparing management:
Low-risk tumours
Perform cystoscopy and computed Weak
tomography urography at three and six
months, and then yearly for five years.
Perform ureteroscopy at three months. Weak
High-risk tumours
Perform cystoscopy, urinary cytology and Weak
computed tomography urography at three
and six months, and then yearly.
Perform ureteroscopy and urinary cytology Weak
in situ at three and six months.

Figure 3: Proposed flowchart for the management of UTUC
UTUC
Diagnosc evaluaon:
CTU, urinary cytology, cystoscopy
Flexible ureteroscopy with biopsies
Low-risk UTUC High-risk UTUC*
RNU template lymphadenectomy
Kidney-sparing surgery:
flexible ureteroscopy or segmental Open Laparoscopic
resecon (prefer open in cT3, cN+)
or percutaneous approach
Recurrence
Single post-operave dose of intravesical

Close and stringent follow-up
chemotherapy
*In patients with a solitary kidney, consider a more

conservative approach.
CTU = computed tomography urography;
RNU = nephroureterectomy.

EAU Guidelines (ISBN: 978-94-92671-01-1), available to all members of

UTUC
status
Mid & Proximal Kidney
1. First treatment option

Mid & Proximal Distal Calyx Renal pelvis
2. Secondary treatment option

Low risk High risk Low risk High risk Low risk High risk Low risk High risk

1. URS • RNU 1. RNU 1. RNU 1. URS • RNU 1. URS • RNU
2. Uretero- LND or or 2. RNU* LND 2. Percuta- LND
uretero- 2. Distal urete- 2. Distal urete- neous
stomy* rectomy rectomy
LND
*In case not amendable to endoscopic management.

Figure 4: Surgical treatment according to location and risk
EAU GUIDELINES ON
MUSCLE-INVASIVE AND METASTATIC
BLADDER CANCER
J.A. Witjes (Chair), M. Bruins, E. Compérat, N.C. Cowan, G. Gakis,

V. Hernández, T. Lebret, A. Lorch, M.J. Ribal (Vice-chair)
A.G. van der Heijden, E. Veskimae
Guidelines Associates: E. Linares Espinós, M. Rouanne,
Y. Neuzillet
Introduction
Optimal treatment strategies for Muscle-invasive Bladder
Cancer (MIBC) require the involvement of a specialist
multidisciplinary team and a model of integrated treatment
strategies to avoid fragmentation of patient care.
Staging and grading systems

The 2017 TNM (Tumour, Node, Metastasis Classification) is
used for staging (Table 1). For grading, the 1973 and 2016 WHO
grading classifications are used (Table 2).
Muscle-invasive and Metastatic Bladder Cancer 37

T - Primary Tumour
Tis Carcinoma in situ: ’flat tumour’
T2 Tumour invades muscle
T2a Tumour invades superficial muscle
(inner half)
T2b Tumour invades deep muscle (outer half)
T3 Tumour invades perivesical tissue
T3a Microscopically
T3b Macroscopically (extravesical mass)
T4 Tumour invades any of the following: prostate
stroma, seminal vesicles, uterus, vagina, pelvic wall,
abdominal wall
T4a Tumour invades prostate stroma, seminal
vesicles, uterus or vagina
T4b Tumour invades pelvic wall or abdominal wall
N – Regional Lymph Nodes
N1 Metastasis in a single lymph node in the true pelvis
(hypogastric, obturator, external iliac, or presacral)
N2 Metastasis in multiple regional lymph nodes in the
true pelvis (hypogastric, obturator, external iliac, or
presacral)
N3 Metastasis in a common iliac lymph node(s)
38 Muscle-invasive and Metastatic Bladder Cancer

M1a Non-regional lymph nodes
M1b Other distant metastasis
Table 2: WHO grading in 1973 and 2016

1973 WHO grading
Grade 1: well differentiated
Grade 2: moderately differentiated
Grade 3: poorly differentiated
2016 WHO grading system (Papillary lesions)

Papillary urothelial neoplasm of low malignant potential
(PUNLMP)
Low-grade (LG) papillary urothelial carcinoma (UC)
High-grade (HG) papillary UC
Pathology of MIBC
Determination of morphological subtypes can be helpful in
assessing the prognosis and treatment options of high-grade
UCs (grade II or grade III) as discussed in these guidelines. The
following differentiation is used:
1. urothelial carcinoma (more than 90% of all cases);
2. urothelial carcinomas with partial squamous and/or
glandular differentiation;
3. micropapillary and microcystic UC;
4. nested variant (including large nested variety);
5. lymphoepithelioma;
6. plasmocytoid, giant cell, signet ring, diffuse,
undifferentiated;
7. some UCs with trophoblastic differentiation;
8. small-cell carcinomas;
9. sarcomatoid carcinomas.

Recommendations for the assessment of Strength rating
tumour specimens
Record the depth of invasion (categories Strong
pT2a and pT2b, pT3a and pT3b or pT4).
Record margins with special attention
paid to the radial margin, prostate, ureter,
urethra and peritoneal fat and uterus and
vaginal top.
Record the number of lymph nodes (LNs),
the number of positive LNs and extranodal
spread.
Record lymphatic or blood vessel invasion
and extranodal extension.
Record the presence of carcinoma in situ.
Recommendations for the primary Strength rating

assessment of presumably invasive
bladder tumours*
Describe all macroscopic features of the Strong
tumour (site, size, number and appearance)
and mucosal abnormalities during
cystoscopy. Use a bladder diagram.
Take a biopsy of the prostatic urethra in Strong
cases of bladder neck tumour, when
bladder carcinoma in situ is present or
suspected, when there is positive cytology
without evidence of tumour in the bladder,
or when abnormalities of the prostatic
urethra are visible.
Take a biopsy at the time of the second Strong
resection, if no biopsy was taken during the
initial procedure.

In women undergoing subsequent Strong
orthotopic neobladder construction,
obtain procedural information (including
histological evaluation) of the bladder neck
and urethral margin, either prior to, or at
the time of cystoscopy.
Specify the grade, depth of tumour Strong
invasion, and whether the lamina propria
and muscle tissue are present in the
specimen in the pathological report.
*F or general information on the assessment of bladder
tumours, see the EAU Guidelines on Non-muscle-invasive
Bladder Cancer.
Recommendations for staging of muscle- Strength rating

invasive bladder cancer (MIBC)
In patients with confirmed MIBC, use Strong
computed tomography (CT) of the chest,
abdomen and pelvis as the optimal form of
staging.
Perform a CT urography for upper tract Strong
evaluation and for staging.
For upper tract evaluation, use diagnostic Strong
ureteroscopy and biopsy only in cases
where additional information will impact
treatment decisions.
Use magnetic resonance urography when Strong
CT urography is contraindicated for reasons
related to contrast administration or
radiation dose.
Use CT or magnetic resonance imaging Strong
(MRI) for staging locally advanced or
metastatic disease in patients in whom
radical treatment is considered.

Use CT to diagnose pulmonary metastases. Strong
Computed tomography and MRI are
generally equivalent for diagnosing local
disease and distant metastases in the
abdomen.
Prognosis
Recommendations for the use of Strength rating

comorbidity scales
Base the decision on bladder-sparing Strong
treatment or radical cystectomy in elderly/
geriatric patients with invasive bladder
cancer on tumour stage and comorbidity.
Assess comorbidity by a validated score, Strong
such as the Charlson Comorbidity Index.
The American Society of Anesthesiologists
score should not be used in this setting.
Disease Management
Recommendations for treatment failure of Strength rating

non-muscle-invasive bladder cancer
Discuss immediate radical treatment in Strong
all T1 tumours at high risk of progression
(i.e., high grade, multifocality, carcinoma
in situ, and tumour size, as outlined in the
EAU Guidelines for Non-muscle-invasive
Bladder Cancer).
Offer radical treatment to all T1 patients Strong
failing intravesical therapy.

Neoadjuvant chemotherapy
Neoadjuvant cisplatin-containing combination chemotherapy
(NAC) improves overall survival (5-8% at five years),
irrespective of the type of definitive treatment used. Currently,
no tools are available to select patients who have a higher
probability of benefitting from NAC. However, NAC has its
limitations regarding patient selection, current development
of surgical techniques, and current chemotherapy
combinations.
Recommendations for neoadjuvant Strength rating

chemotherapy
Offer NAC for T2-T4a, cN0M0 bladder Strong
cancer. In this case, always use cisplatin-
based combination therapy.
Do not offer NAC to patients who are Strong
ineligible for cisplatin-based combination
chemotherapy.
Recommendations for pre- and post- Strength rating

operative radiotherapy in MIBC
Do not offer pre-operative radiotherapy (RT) Strong
to improve survival.
Offer pre-operative RT for operable MIBC Weak
since it can result in tumour downstaging
after four to six weeks.
Radical cystectomy and urinary diversion

Contraindications for orthotopic bladder substitution are
positive margins at the level of urethral dissection, positive
margins anywhere on the bladder specimen (in both sexes),
if the primary tumour is located at the bladder neck or in the

urethra (in women), or if tumour extensively infiltrates the
prostate (in men).
Recommendations for radical cystectomy Strength rating

and urinary diversion
Do not delay cystectomy for > 3 months Strong
as it increases the risk of progression and
cancer-specific mortality.
Before cystectomy, fully inform the patient Strong
about the benefits and potential risks of
all possible alternatives. The final decision
should be based on a balanced discussion
between the patient and the surgeon.
Do not offer an orthotopic bladder Strong
substitute diversion to patients who have
a tumour in the urethra or at the level of
urethral dissection.
Do not offer pre-operative radiotherapy Strong
when subsequent cystectomy with urinary
diversion is planned.
Do not offer sexual-preserving cystectomy Strong
as standard therapy for MIBC.
Offer sexual-preserving techniques to men Strong
motivated to preserve their sexual function
since the majority will benefit.
Select patients based on: Strong
• organ-confined disease;
• absence of any kind of tumour at the
level of the prostate, prostatic urethra
or bladder neck.
Do not offer pelvic organ-preserving radical Strong
cystectomy (RC) to female patients as
standard therapy for MIBC.

Offer sexual-preserving techniques to Weak
female patients motivated to preserve
their sexual function since the majority will
benefit.
Select patients based on: Strong
• organ-confined disease;
• absence of tumour in bladder neck or
urethra.
Pre-operative bowel preparation is not Strong
mandatory. “Fast track” measurements may
reduce the time of bowel recovery.
Offer RC in T2-T4a, N0M0, and high-risk Strong
non-MIBC.
Perform a lymph node dissection as an Strong
integral part of cystectomy.
Do not preserve the urethra if margins are Strong
positive.
Recommendations for laparoscopic/ Strength rating

robotic-assisted laparoscopic cystectomy
Inform the patient of the advantages and Strong
disadvantages of open radical cystectomy
and robot-assisted radical cystectomy
(RARC) to allow selection of the proper
procedure.
Select experienced centres, not specific Strong
techniques, both for RARC and ORC.

Figure 1: Flow chart for the management of T2-T4a N0M0
urothelial bladder cancer
Diagnosis 1 – Males: biopsy apical prostac urethra

• Cystoscopy and tumour resecon or frozen secon during surgery
• Evaluaon of urethra1
• CT imaging of abdomen, chest, UUT – Females : biopsy of proximal urethra
• MRI can be used for local staging or frozen secon during surgery
pT2N0M0 selected paents

Findings - Mulmodality bladder-sparing therapy
• pT2-4a, clinical N0M0 urothelial can be considered for T2 tumours
carcinoma of the bladder (Note: alternave, not the standard
opon)
Neoadjuvant chemotherapy2
• Should be considered in selected 2 - Neoadjuvant radiotherapy is not
paents recommended
• 5-8% five year survival benefit
Radical cystectomy
• Know general aspects of surgery
o Preparaon
o Surgical technique
o Integrated node dissecon
o Urinary diversion
o Timing of surgery
• A higher case load improves outcome
Direct adjuvant chemotherapy

• Not indicated aer cystectomy
CT = computed tomography; MRI = magnetic resonance

imaging; UUT = upper urinary tract.

Bladder-sparing treatments for localised disease
Transurethral resection of bladder tumour
Transurethral resection of bladder tumour alone is only
possible as a therapeutic option if tumour growth is limited
to the superficial muscle layer and if restaging biopsies are
negative for residual tumour.
External beam radiotherapy

External beam radiotherapy alone should only be considered
as a therapeutic option when the patient is unfit for
cystectomy or a multimodality bladder-preserving approach.
Radiotherapy can also be used to stop bleeding from the
tumour when local control cannot be achieved by
transurethral manipulation due to extensive local tumour
growth.
Chemotherapy and best supportive care

Complete and partial local responses have been reported with
cisplatin-based chemotherapy as primary therapy for locally
advanced tumours in highly selected patients.
Multimodality treatment
In a highly selected patient population, long-term survival
rates of multimodality treatment are comparable to those of
early cystectomy. Delaying surgery can compromise survival
rates.
Recommendations for bladder-sparing Strength rating

treatments for localised disease
Do not offer transurethral resection of Strong
bladder tumour alone as a curative
treatment option as most patients will not
benefit.
Do not offer radiotherapy alone as primary Strong
therapy for localised bladder cancer.

Do not offer chemotherapy alone as primary Strong
therapy for localised bladder cancer.
Offer surgical intervention or multimodality Strong
treatments (MMT) as primary curative
therapeutic approaches since they are
more effective than radiotherapy alone.
Offer MMT as an alternative in selected, Strong
well-informed and compliant patients,
especially for whom cystectomy is not an
option.
Surgically non-curable tumours

Palliative radical cystectomy for metastatic disease
Primary radical cystectomy (RC) in T4b bladder cancer is not
a curative option. If there are symptoms, RC may be a
therapeutic/palliative option. Intestinal or non-intestinal forms
of urinary diversion can be used, with or without palliative
cystectomy.

Offer radical cystectomy as a palliative Weak
treatment to patients with inoperable
locally advanced tumours (T4b).
Offer palliative cystectomy in patients with Weak
symptoms.
Adjuvant Chemotherapy

Offer adjuvant cisplatin-based combination Strong
chemotherapy to patients with pT3/4
and/or pN+ disease if no neoadjuvant
chemotherapy has been given.

Metastatic disease

First-line treatment for fit patients
Use cisplatin-containing combination Strong
chemotherapy with GC, MVAC, preferably
with G-CSF, HD-MVAC with G-CSF or PCG.
Do not use carboplatin and non-platinum Strong
combination chemotherapy.
First-line treatment in patients ineligible (unfit) for cisplatin:
Use checkpoint inhibitors pembrolizumab Strong
or atezolizumab.
Use carboplatin combination Weak
chemotherapy.
Second-line treatment
Offer checkpoint inhibitors pembrolizumab Strong
or atezolizumab to patients progressing
during or after platinum-based
combination chemotherapy for metastatic
disease. Alternatively, offer treatment
within a clinical trial setting.
Offer checkpoint inhibitor nivolumab to Strong
patients progressing during or after
platinum-based combination chemotherapy
for metastatic disease. Alternatively, offer
treatment within a clinical trial setting.
Offer zoledronic acid or denosumab to Weak
treat bone metastases.

Subsequent treatment
Only offer vinflunine to patients for Weak
metastatic disease as second-line
treatment if immunotherapy or
combination chemotherapy is not feasible.
Alternatively, offer vinflunine as
subsequent treatment line, or offer
treatment within a clinical trial setting or
best supportive care.
GC = gemcitabine plus cisplatin; G-CSF = granulocyte colony-
stimulating factor; HD-MVAC = high-dose methotrexate,
vinblastine, adriamycin plus cisplatin; PCG = paclitaxel,
cisplatin, gemcitabine.

Figure 2: Flow chart for the management of metastatic
urothelial cancer
Paent characteriscs
PS 0-1/ 2/ >2
GFR ≥/< 60 mL/min
Comorbidies
CISPLATIN?
YES NO NO
PS 0-1 and PS 2 or PS ≥ 2 and

GFR ≥ 60 mL/min GFR < 60 mL/min GFR < 60 mL/min
1. carboplan and (no comb chemo studies)
STANDARD GC gemcitabine
MVAC 2. pembrolizumab Monotherapy with either:
HD MVAC 3. atezolizumab 1. pembrolizumab
PCG 4. Alternate regimens (no 2. atezolizumab
comb chemo, studies, Or
monotherapy, BSC) Best supporve care
independent of the me of progression aer first-line treatment
PS 0-1 PS ≥ 2
Progression (independent a. Consider

of the me interval aer immunotherapy
receiving first-line b. Clinical trial
chemotherapy), adequate c. Best supporve care
renal funcon
Standard regimens
1. pembrolizumab
2. atezolizumab
3. nivolumab
Or
1. Clinical trial
2. Comb chemotherapy
3. Monotherapies
Subsequent treatment
1. Chemotherapy
2. Immunotherapy, if not
given as second-line
treatment
3. Clinical trial
4. Best supporve care
BSC = best supportive care; GC = gemcitabine plus cisplatin;

GFR = glomerular filtration rate; HD MVAC = high-dose
methotrexate, vinblastine, adriamycin plus cisplatin; MVAC =
methotrexate, vinblastine,adriamycin plus cisplatin; PCG =
paclitaxel, cisplatin, gemcitabine; PS = performance status.
Health-related quality-of-life (HRQoL)
Important determinants of (subjective) quality of life are a
patient’s personality, coping style and social support.

Use validated questionnaires to assess Strong
HRQoL in patients with MIBC.
Offer a continent urinary diversion unless Strong
a patient’s comorbidities, tumour variables
and coping abilities present clear
contraindications.
Pre-operative patient information, patient Strong
selection, surgical techniques, and
careful post-operative follow-up are the
cornerstones for achieving good long-term
results.
Provide clear and exhaustive information Strong
on all potential benefits and side-effects,
allowing patients to make informed
decisions. Encourage patients to actively
participate in the decision-making process.

EAU Guidelines (978-94-92671-01-1), available to all members of the
European Association of Urology at their website,

EAU-ESTRO-ESUR-SIOG GUIDELINES
ON PROSTATE CANCER
(Text update March 2018)
N. Mottet (Chair), R.C.N. van den Bergh, E. Briers (Patient

Representative), L. Bourke, P. Cornford (Vice-chair), M. De Santis,
S. Gillessen, A. Govorov, J. Grummet, A.M. Henry, T.B. Lam,
M.D. Mason, H.G. van der Poel, T.H. van der Kwast, O. Rouvière,
T. Wiegel
Guidelines Associates: T. Van den Broeck, M. Cumberbatch,
N. Fossati, T. Gross, M. Lardas, M. Liew, L. Moris, I.G. Schoots,
P.M. Willemse
Introduction
Prostate cancer (PCa) is a complex disease, in which disease
characteristics, age, comorbidities and individual patient
preference will impact treatment choice. All available manage-
ment options need to be discussed, in full, with the patient.
Epidemiology and Risk Prevention

Prostate cancer is the second most common cancer in males.
It is a major health concern, especially in developed countries
due to the greater proportion of elderly men in the general
population, and the potential risk of over-treatment following
early diagnosis. There are three well-established risk factors
for PCa: increasing age, ethnic origin, and genetic
predisposition. There is currently no high-level evidence that
preventative measures may reduce the risk of PCa.
Classification and Staging Systems

The 2017 Tumour Node Metastasis (TNM) classification is used
for staging (Table 1).
Prostate Cancer 53
Table 1: 2017 TNM classification
T - Primary Tumour
T1 Clinically inapparent tumour that is not palpable
T1a Tumour incidental histological finding in 5% or
less of tissue resected
T1b Tumour incidental histological finding in more
than 5% of tissue resected
T1c Tumour identified by needle biopsy (e.g. because
of elevated prostate-specific antigen [PSA])
T2 Tumour that is palpable and confined within the
prostate
T2a Tumour involves one half of one lobe or less
T2b Tumour involves more than half of one lobe, but
not both lobes
T2c Tumour involves both lobes
T3 Tumour extends through the prostatic capsule*
T3a Extracapsular extension (unilateral or bilateral)
including microscopic bladder neck
involvement
T3b Tumour invades seminal vesicle(s)
T4 Tumour is fixed or invades adjacent structures other
than seminal vesicles: external sphincter, rectum,
levator muscles, and/or pelvic wall
N - Regional Lymph Nodes1
N1 Regional lymph node metastasis
54 Prostate Cancer
M - Distant Metastasis2
M1a Non-regional lymph node(s)
M1b Bone(s)
M1c Other site(s)
* Invasion into the prostatic apex or into (but not beyond) the
prostatic capsule is not classified as T3, but as T2.
1 Metastasis no larger than 0.2 cm can be designated pNmi.
2 When more than one site of metastasis is present, the most
advanced category is used. (p)M1c is the most advanced

category.
Pathological staging (pTNM) is based on histopathological

tissue assessment and largely parallels the clinical TNM,
except for clinical stage T1c and the T2 substages. All
histopathologically confirmed organ-confined PCas after
radical prostatectomy (RP) are pathological stage T2 and the
current UICC no longer recognises pT2 substages.
Table 2: EAU risk groups for biochemical recurrence of

localised and locally advanced prostate cancer
Definition
Low-risk Intermediate- High-risk
risk
PSA < 10 ng/mL PSA 10-20 ng/mL PSA > 20 ng/mL any PSA
and GS < 7 or GS 7 or GS > 7 any GS
(ISUP grade 1) (ISUP grade 2/3) (ISUP grade 4/5) cT3-4 or cN+
and cT1-2a or cT2b or cT2c
Localised Locally
advanced
GS = Gleason score; ISUP = International Society for Urological
Pathology; PSA = prostate-specific antigen.
Prostate Cancer 55
Recommendations for screening and early Strength rating
detection
Do not subject men to prostate-specific Strong
antigen (PSA) testing without counselling
them on the potential risks and benefits.
Offer an individualised risk-adapted Strong
strategy for early detection to a well-
informed man with a good performance
status (PS) and a life-expectancy of at least
ten to fifteen years.
Offer early PSA testing in well-informed Strong
men at elevated risk of having PCa:
• men > 50 years of age;
• men > 45 years of age and a family
history of PCa;
• African-Americans > 45 years of age.
Offer a risk-adapted strategy (based on Weak
initial PSA level), with follow-up intervals of
two years for those initially at risk:
• men with a PSA level of > 1 ng/mL at 40
years of age;
• men with a PSA level of > 2 ng/mL at 60
years of age.
Postpone follow-up to eight years in those
not at risk.
Stop early diagnosis of PCa based on life Strong
expectancy and PS; men who have a
life-expectancy of < 15 years are unlikely to
benefit.
56 Prostate Cancer
Diagnostic Evaluation
Clinical diagnosis
Prostate cancer is usually suspected on the basis of digital
rectal examination (DRE) and/or PSA levels. Definitive
diagnosis depends on histopathological verification of
adenocarcinoma in prostate biopsy cores or unexpected
discovery in specimens from transurethral resection of
the prostate (TURP) or prostatectomy for benign prostatic
enlargement.
The decision whether to proceed with further diagnostic
or staging work-up is guided by which treatment options are
available to the patient, taking the patient’s life expectancy
into consideration. Diagnostic procedures that will not affect
the treatment decision can usually be avoided.
A biopsy pathology report includes the type of carcinoma and

parameters describing its extent (e.g. proportion of positive
cores, percentage or mm of carcinoma involvement per core)
as well as Gleason score (GS) per biopsy site and global GS.
Reporting of a radical prostatectomy (RP) specimen includes
type of carcinoma, global GS, pathological stage and surgical
margin status.
The International Society of Urological Pathology (ISUP) World

Health Organization (WHO) 2014 grade groups were adopted
which allow patients to better understand the behaviour of
their diagnosed prostate carcinoma, while separating GS 7
adenocarcinoma into two prognostically very distinct cat-
egories; grade group 2 for GS 7(3+4) and grade group 3 for GS
7(4+3) (see Table 3).
Prostate Cancer 57
Table 3: ISUP 2014 grade groups
Gleason score Grade group

2-6 1
7 (3+4) 2
7 (4+3) 3
8 (4+4 or 3+5 or 5+3) 4
9-10 5
Recommendations for clinical diagnosis Strength rating

of PCa
Do not use transurethral resection of the Strong
prostate as a tool for cancer detection.
Use the International Society of Urological Strong
Pathology (ISUP) 2014 Gleason grading
system for grading of PCa.
In symptomatic men, base the initial Strong
decision to perform a biopsy on prostate-
specific antigen testing and digital rectal
examination.
Do not initially offer transition zone Weak
biopsies due to low detection rates.
For initial diagnosis, perform a core biopsy Strong
of ten to twelve systematic transrectal
or transperineal peripheral zone biopsies
under ultrasound guidance.
Perform transrectal prostate needle Strong
biopsies under antibiotic protection.
Use a local anaesthetic by periprostatic Strong
infiltration for transrectal prostate needle
biopsies.
58 Prostate Cancer
Ensure that prostate core biopsies from Strong
different sites are submitted separately for
processing and pathology reporting.
Adhere to the 2010 ISUP Consensus Strong
Meeting Guidelines for processing and
reporting of prostatectomy specimens.
Recommendations for processing Strength rating

prostatectomy specimens
Ensure total embedding, by conventional Strong
(quadrant) or whole-mount sectioning.
Ink the entire surface before cutting, to Strong
evaluate the surgical margin.
Examine the apex and base separately, Strong
using the cone method with sagittal or
radial sectioning.
Recommendations for repeat-biopsy Strength rating

imaging
Before repeat biopsy, perform Strong
multiparametric magnetic resonance
imaging (mpMRI) when clinical suspicion of
PCa persists in spite of negative biopsies.
During repeat biopsy include Strong
systematic biopsies and targeting of any
mpMRI lesions seen.
Guidelines for staging
Any risk group staging Strength rating

Do not use computed tomography and Strong
transrectal ultrasound for local staging.
Prostate Cancer 59
Low-risk localised PCa Strength rating
Do not use additional imaging for staging Strong
purposes.
Intermediate-risk PCa Strength rating

In predominantly Gleason pattern 4 Weak
(≥ ISUP 3) use prostate multiparametric
magnetic resonance imaging (mpMRI) for
local staging.
In predominantly Gleason pattern 4, Weak
include at least a cross-sectional
abdominopelvic imaging and bone-scan
for metastatic screening.
High-risk localised PCa/locally advanced Strength rating

PCa
Use prostate mpMRI for local staging. Strong
Perform metastatic screening including at Strong
least cross-sectional abdominopelvic
imaging and a bone-scan.
60 Prostate Cancer
Figure 1: Decision-making based on health status
assessment (men > 70 years)*
Screening with G8 and mini-COGTM
Score > 14 Score < 14

No simplified Simplified
geriatric geriatric
evalua on is evalua on is
needed mandatory
Reversible= Nonreversible =
- Abnormal ADL: 1 or 2 - Abnormal ADL: > 2
- Weight loss 5–10% - Weight loss > 10%
- Comorbidi es CISR-G - Comorbidi es CISR-G
grades 1-2 grades 3-4
CGA then
geriatric
intervenon
Disabled/severe
Fit Frail
comorbidies
*Reproduced with permission of Elsevier, from Droz J-P, et al.

Eur Urol 2017:72(4); 521.
Mini-COGTM = cognitive test; ADL = activities of daily living;
CIRS-G = cumulative illness rating score-geriatrics;
CGA = comprehensive geriatric assessment.
Prostate Cancer 61
Recommendations for evaluating health Strength rating
status and life expectancy
Systematically screen the health status of Strong
older (> 70 years) men with PCa (Figure 1).
Use the Geriatric-8 and mini-COG tools for Weak
health status screening.
Perform a full specialist geriatric evaluation Strong
in patients with G8 score ≤ 14.
Consider standard treatment in frail Weak
patients with reversible impairments (after
resolution of geriatric problems) similar to
fit patients, if life expectancy is > 10 years.
Offer adapted treatment in patients with
irreversible impairment.
Offer palliation in patients with poor health
status.
Disease Management
Deferred treatment
Many men with localised PCa will not benefit from definitive
treatment, and 45% of men with PSA-detected PCa may be
candidates for deferred management.
In men with comorbidity and a limited life expectancy,
treatment of localised PCa may be deferred to avoid loss of
quality of life (QoL).
Primary treatment of PCa
General recommendations for active Strength rating

treatment
Inform patients that no active treatment Strong
modality has shown superiority over any
other management options in terms of
survival.
62 Prostate Cancer
Inform patients that all active treatments Strong
have side effects.
Surgical treatment
Inform patients that no surgical approach Strong
(open, laparoscopic- or robotic radical
prostatectomy) has clearly shown
superiority in terms of functional or
oncological results.
Perform an extended pelvic LND (ePLND), Strong
when a LND is deemed necessary.
Do not perform nerve-sparing surgery when Strong
there is a risk of extracapsular extension
(based on cT stage, GS, nomogram,
multiparametric magnetic resonance
imaging).
Do not offer neoadjuvant androgen Strong
deprivation therapy before surgery.
Radiotherapeutic treatment
Offer intensity-modulated radiation therapy Strong
(IMRT) or volumetric arc external-beam
radiotherapy (VMAT) for definitive
treatment of PCa by external-beam
radiation therapy (EBRT).
Only offer moderate hypofractionation Strong
(HFX) with IMRT/VMAT, including image-
guided radiation therapy (IGRT) to the
prostate, to carefully selected patients with
localised disease.
Ensure that moderate HFX adheres to Strong
radiotherapy (RT) protocols from trials with
equivalent outcome and toxicity, i.e.
60 Gy/20 fractions in four weeks or
70 Gy/28 fractions in six weeks.
Prostate Cancer 63
Active therapeutic options outside surgery and radiotherapy
Only offer cryotherapy and high-intensity Strong
focused ultrasound within a clinical trial
setting.
Only offer focal therapy within a clinical Strong
trial setting.
Guidelines for first line treatment of various Strength

disease stages rating
Low-risk disease
Watchful Offer a WW policy to Strong
waiting (WW) asymptomatic patients with
a life expectancy < 10 years
(based on comorbidities).
Active Offer AS to patients suitable for Strong
surveillance curative treatment but with
(AS) low-risk PCa.
Perform multiparametric Strong
magnetic resonance imaging
(mpMRI) before a confirmatory
biopsy.
During confirmatory biopsy Strong
include systematic and targeted
biopsies.
Base follow up on digital rectal Strong
examination, prostate-specific
antigen (PSA) and repeat
biopsies.
Counsel patients about the Strong
possibility of needing further
treatment in the future.
64 Prostate Cancer
Active Offer surgery and radiotherapy Weak
treatment (RT) as alternatives to AS to
patients suitable for such
treatments and who accept a
trade-off between toxicity and
prevention of disease
progression.
Pelvic Do not perform a PLND Strong
lymph node (estimated risk for pN+ < 5%).
dissection
(PLND)
Radiotherapy Offer low-dose rate (LDR) Strong
brachytherapy to patients with
low-risk PCa, without a previous
transurethral resection of the
prostate (TURP) and with a good
International Prostatic Symptom
Score (IPSS) and a prostate
volume < 50 mL.
Use intensity-modulated Strong
radiation therapy (IMRT) with a
total dose of 74-80 Gy, without
androgen deprivation therapy
(ADT).
Offer moderate hypofractionation Strong
(HFX) (68 Gy/20 fx in four weeks
or 70 Gy/28 fractions (fx) in six
weeks) as an alternative
treatment option.
Other options Only offer whole gland treatment Strong
(such as cryotherapy, HIFU, etc.)
or focal treatment within a
clinical trial setting.
Prostate Cancer 65
Intermediate-risk disease
Active Offer AS to highly selected Weak
surveillance patients (< 10% pattern 4)
accepting the potential
increased risk of further
metastases.
Radical Offer RP to patients with Strong
prostatectomy intermediate-risk disease and
(RP) a life expectancy > 10 years.
Offer nerve-sparing surgery strong
to patients with a low risk of
extracapsular disease (refer to
nomograms).
Extended Perform an ePLND in Strong
pelvic intermediate-risk disease if the
lymph node estimated risk for positive lymph
dissection nodes exceeds 5%.
(ePLND)
Radiotherapy Offer LDR brachytherapy to Strong
selected patients; patients
without a previous TURP and
with a good IPSS and a prostate
volume < 50 mL.
For EBRT, use a total dose of Strong
76-78 Gy, in combination with
short-term neoadjuvant plus
concomitant ADT (four to six
months).
In patients not willing to undergo Weak
ADT, use an escalated dose of
EBRT (76-80 Gy) or a
combination with brachytherapy.
66 Prostate Cancer
Other options Only offer whole gland treatment Strong
(such as cryotherapy, HIFU, etc.)
or focal treatment within a
clinical trial setting.
High-risk localised disease
Radical Offer RP to patients with high- Strong
prostatectomy risk localised PCa and a life
expectancy of > 10 years only as
part of multi-modal therapy.
Extended Perform an ePLND in high-risk Strong
pelvic disease.
lymph node Do not perform a frozen section Strong
dissection of nodes during RP to decide
whether to proceed with, or
abandon, the procedure.
Radiotherapy In patients with high-risk Strong
localised disease, use ERBT with
76-78 Gy in combination with
long-term ADT (two to three
years).
In patients with high-risk Weak
localised disease, use EBRT with
brachytherapy boost (either
HDR or LDR), in combination
with long-term ADT (two to
three years).
Other options Do not offer either whole gland Strong
or focal treatment to high-risk
patients.
Do not use ADT monotherapy in Strong
asymptomatic patients.
Prostate Cancer 67
Locally-advanced disease
Radical Offer RP to highly selected Strong
prostatectomy patients with (cT3b-T4 N0 or any
T N1) only as part of multi-modal
therapy.
Extended Perform an ePLND in high-risk Strong
pelvic PCa.
lymph node Do not perform a frozen section Strong
dissection of nodes during RP to decide
whether to proceed with, or
abandon, the procedure.
Radiotherapy In patients with locally advanced Strong
cN0 disease, offer RT in
combination with long-term
ADT.
Offer long-term ADT for two to Weak
three years.
Other options Do not offer whole gland Strong
treatment or focal treatment to
high-risk patients.
Only offer ADT monotherapy to Strong
those patients unwilling or
unable to receive any form of
local treatment and who are
either symptomatic or
asymptomatic, but with a
PSA-doubling time (DT) over
twelve months or a PSA
> 50 ng/mL or a poorly
differentiated tumour.
68 Prostate Cancer
Adjuvant treatment after radical prostatectomy
Only discuss adjuvant treatment Strong
in men with a post-operative
PSA < 0.1 ng/mL.
Do not prescribe adjuvant ADT Strong
in pN0 patients.
Offer adjuvant EBRT to the Strong
surgical field to patients at
increased risk of local relapse:
pT3 pN0 with positive margins
(highest impact), and/or invasion
of the seminal vesicles.
Discuss three management Weak
options with patients with pN+
disease after an ePLND, based
on nodal involvement
characteristics:
1. Offer adjuvant ADT for node-
positive (pN+).
2. Offer adjuvant ADT with
additional radiotherapy.
3. Offer observation (expectant
management) to a patient
after eLND and ≤ 2 nodes with
microscopic involvement,
and a PSA < 0.1 ng/mL and
absence of extranodal
extension.
Prostate Cancer 69
Non-curative or palliative treatments in a first-line setting
Localised disease
Watchful Offer WW to asymptomatic Strong
waiting patients not eligible for local
curative treatment and those
with a short life expectancy.
While on WW, base the decision Strong
to start non-curative treatment
on symptoms and disease
progression.
Locally advanced disease
Watchful Offer a deferred treatment Strong
waiting policy using ADT monotherapy
to M0 asymptomatic patients
with a PSA-DT > twelve months,
a PSA < 50 ng/mL and well
differentiated tumour, who are
unwilling or unable to receive
any form of local treatment.
Metastatic disease in a first-line setting
Symptomatic In M1 symptomatic patients, Strong
patients offer immediate systemic
treatment to palliate symptoms
and reduce the risk for
potentially serious sequelae of
advanced disease (spinal cord
compression, pathological
fractures, ureteral obstruction,
and extra-skeletal metastasis).
70 Prostate Cancer
Asymptomatic In M1 asymptomatic patients, Strong
patients offer immediate systemic
treatment to improve survival,
defer progression to a
symptomatic stage and prevent
serious disease progression-
related complications.
In M1 asymptomatic patients, Weak
discuss deferred castration with
a well-informed patient since
it lowers the treatment side
effects, provided the patient is
closely monitored.
All M1 patients Offer LHRH antagonists, Weak
especially to patients with an
impending spinal cord
compression or bladder outlet
obstruction.
In M1 patients treated with a Weak
LHRH agonist, offer short-term
administration of anti-androgens
to reduce the risk of the ‘flare-
up’ phenomenon.
Do not offer anti-androgen Strong
monotherapy for M1 disease.
Offer castration combined with Strong
chemotherapy (docetaxel) to
all patients whose first
presentation is M1 disease and
who are fit enough for docetaxel.
Prostate Cancer 71
Offer castration combined Strong
with abiraterone acetate plus
prednisone to all patients whose
first presentation is M1 disease
and who are fit enough for the
regimen.
Offer castration alone, with or Strong
without an anti-androgen, to
patients unfit for, or unwilling to
consider, castration combined
with docetaxel or abiraterone
acetate plus prednisone.
M1 patients In asymptomatic M1 patients, Strong
receiving only offer intermittent treatment
Intermittent to highly motivated men, with
treatment a major PSA response after the
induction period.
• In M1 patients, follow the Weak
schedules used in published
clinical trials on timing of
intermittent treatment.
• Stop treatment when the PSA
level is < 4 ng/mL after six to
seven months of treatment.
• Resume treatment when the
PSA level is > 10-20 ng/mL (or
returned to the initial level of
< 20 ng/mL).
Do not use castration combined Strong
with any local treatment
(RT/surgery) outside an
investigational setting except
for symptom control.
72 Prostate Cancer
Guidelines for second-line and palliative treatments
Biochemical recurrence after treatment with curative intent

Biochemical Offer AS and possibly delayed Strong
recurrence salvage RT (SRT) to patients with
after radical a biochemical recurrence and
prostatectomy favourable prognostic factors
(RP) (≤ pT3a, time to biochemical
recurrence > three year, PSA-DT
> twelve months, GS ≤ 7), who
may not benefit from
intervention.
Treat patients with a PSA rise Strong
from the undetectable range
with SRT. The total dose of SRT
should be at least 66 Gy and
should be given early
(PSA < 0.5 ng/mL).
Biochemical Treat highly selected patients Weak
recurrence with localised PCa and a
after RT histologically proven local
recurrence with salvage RP (SRP).
Salvage RP should only be Strong
performed in experienced
centres.
Do not offer HIFU, cryosurgical Strong
ablation and salvage brachy-
therapy to patients with proven
local recurrence since it is still
experimental.
Systemic Do not offer ADT to M0 patients Strong
salvage with a PSA-DT > twelve months.
treatment
Prostate Cancer 73
Life-prolonging treatments of castration-resistant disease
Ensure that testosterone levels Strong
are confirmed to be < 50 ng/mL,
before diagnosing castration-
resistant PCa (CRPC).
Do not treat patients for non- Strong
metastatic CRPC outside of a
clinical trial.
Counsel, manage and treat Strong
patients with metastatic CRPC
(mCRPC) in a multidisciplinary
team.
Treat patients with mCRPC with Strong
life-prolonging agents.
Base the choice of first-line
treatment on the performance
status (PS), symptoms,
comorbidities, location and
extent of disease, patient
preference, and on the previous
treatment for hormone-sensitive
PCa (alphabetical order:
abiraterone, docetaxel,
enzalutamide, radium-223,
sipuleucel-T).
Cytotoxic treatments of castration-resistant disease
Counsel, manage and treat Strong
patients with mCRPC in a
multidisciplinary team.
Offer patients with mCRPC who Strong
are candidates for cytotoxic
therapy docetaxel with
75 mg/m2 every three weeks.
74 Prostate Cancer
In patients with mCRPC and Strong
progression following docetaxel
chemotherapy offer further life-
prolonging treatment options,
which include abiraterone,
cabazitaxel, enzalutamide and
radium-223.
Base second-line treatment Strong
decisions of mCRPC on pre-
treatment PS, symptoms, patient
preference, comorbidities and
extent of disease.
Supportive care of castration-resistant disease
Offer bone protective agents Strong
to patients with mCRPC and
skeletal metastases to prevent
osseous complications.
Offer calcium and vitamin D Strong
supplementation when
prescribing either denosumab
or bisphosphonates.
Treat painful bone metastases Strong
early on with palliative measures
such as EBRT, and adequate use
of analgesics.
In patients with spinal cord Strong
compression start immediate
high-dose corticosteroids and
assess for spinal surgery
followed by irradiation. Offer
radiation therapy alone if
surgery is not appropriate.
Prostate Cancer 75
Follow-up after treatment with curative intent
• After RP, PSA should be undetectable (< 0.1 ng/mL).
A PSA of > 0.1 ng/mL after RP is a signal of residual prostate
tumour tissue. After an undetectable PSA is obtained
following RP, a PSA > 0.4 ng/mL and rising, best predicts
further metastases.
• After RT, an increase in PSA > nadir + 2 ng/mL best predicts
further metastases.
• Palpable nodules and increasing serum PSA are often signs
of local recurrence.
Recommendations for follow-up Strength rating

Routinely follow-up asymptomatic patients, Strong
by obtaining a disease-specific history
and serum prostate-specific antigen (PSA)
measurement. These should be performed
at three, six and twelve months after
treatment, then every six months until
three years, and then annually.
During follow up, perform a systematic Weak
digital rectal examination (DRE) after
surgery if unfavourable pathology
(> pT3, pN1, Gleason ≥ 8).
During follow up, perform a systematic Strong
DRE after radiotherapy.
At recurrence, only image to detect local Strong
recurrence if it affects treatment planning.
Do not routinely offer bone scans and Strong
other imaging modalities to asymptomatic
patients if there are no signs of biochemical
relapse. In case patients have bone pain or
other symptoms of possible progression,
restaging should be considered
irrespective of serum PSA level.
76 Prostate Cancer
Recommendations for follow-up during Strength rating
hormonal treatment
Evaluate patients at three to six months Strong
after the initiation of treatment.
The follow-up strategy must be Strong
individualised based on stage of disease,
prior symptoms, prognostic factors and the
treatment given.
In patients with stage M0 disease, schedule Strong
follow-up every six months. As a minimum
requirement, include a disease-specific
history, DRE and serum PSA determination
in the diagnostic work-up.
In patients with stage M1 disease, schedule Strong
follow-up every three to six months. As a
minimum requirement, include a disease-
specific history, DRE, serum PSA,
haemoglobin, serum creatinine and
alkaline phosphatase measurements in
the diagnostic work-up. The testosterone
level should be checked, especially during
the first year.
Counsel patients (especially with M1b Strong
status) about the clinical signs suggestive
of spinal cord compression.
When disease progression is suspected, Strong
adapt/individualise follow up.
In patients with suspected progression, Strong
assess the testosterone level. By definition,
castration resistant PCa (CRPC) requires a
testosterone level < 50 ng/dL (< 1 mL/L).
Do not offer routine imaging to otherwise Strong
stable asymptomatic patients.
Prostate Cancer 77
Quality of Life
Treating PCa can affect an individual both physically and
mentally, as well as his close relations and his work or
vocation. These multifaceted issues all have a bearing on his
perception of ‘quality of life (QoL)’. Prostate cancer care should
not be reduced to focusing on the organ in isolation. Taking
QoL into consideration relies on understanding the patient’s
wishes and preferences so that optimal treatment proposals
can be formulated and discussed. There is clear evidence of
unmet needs and ongoing support requirements for some
men after diagnosis and treatment for PCa.

EAU Guidelines (ISBN 978-94-92671-01-1), available to all members of
78 Prostate Cancer
EAU GUIDELINES ON RENAL CELL
CARCINOMA
B. Ljungberg (Chair), L. Albiges, K. Bensalah, A. Bex (Vice-chair),

R.H. Giles (Patient Advocate), M. Hora, M.A. Kuczyk, T. Lam,
L. Marconi, A.S. Merseburger, T. Powles, M. Staehler, A. Volpe
Guidelines Associates: Y. Abu-Ghanem, S. Dabestani,
S. Fernández-Pello Montes, F. Hofmann, R. Tahbaz
Epidemiology
The use of imaging techniques such as ultrasound (US) and
computerised tomography (CT) has increased the detection
of asymptomatic renal cell cancer (RCC). The peak incidence
of RCC occurs between 60 and 70 years of age, with a 3 : 2
ratio of men to women. Aetiological factors include lifestyle
factors, such as smoking, obesity and hypertension. Having a
first-degree relative with RCC is associated with a significantly
increased risk of RCC.
Staging system
The current UICC 2017 TNM (Tumour Node Metastasis)
classification is recommended for the staging of RCC (Table 1).
Renal Cell Carcinoma 79

Table 1: The 2017 TNM staging classification system
T - Primary Tumour
T1 Tumour ≤ 7 cm or less in greatest dimension, limited to
the kidney
T1a Tumour ≤ 4 cm or less
T1b Tumour > 4 cm but ≤ 7 cm
T2 Tumour > 7 cm in greatest dimension, limited to the
kidney
T2a Tumour > 7 cm but ≤ 10 cm
T2b Tumours > 10 cm, limited to the kidney
T3 Tumour extends into major veins or perinephric tissues
but not into the ipsilateral adrenal gland and not
beyond Gerota fascia
T3a Tumour grossly extends into the renal vein or
its segmental (muscle-containing) branches, or
tumour invades perirenal and/or renal sinus fat
(peripelvic), but not beyond Gerota fascia
T3b Tumour grossly extends into the vena cava below
diaphragm
T3c Tumour grossly extends into vena cava above the
diaphragm or invades the wall of the vena cava
T4 Tumour invades beyond Gerota fascia (including
contiguous extension into the ipsilateral adrenal gland)
N - Regional Lymph Nodes
N1 Metastasis in regional lymph node(s)
80 Renal Cell Carcinoma

TNM stage grouping
Stage I T1 N0 M0
Stage II T2 N0 M0
Stage III T3 N0 M0
T1, T2, T3 N1 M0
Stage IV T4 Any N M0
Any T Any N M1
A help desk for specific questions about TNM classification is
available at http://www.uicc.org/tnm.
Clinical Diagnosis
Many renal masses remain asymptomatic until late disease
stages. The classic triad of flank pain, visible haematuria,
and palpable abdominal mass is rare and correlates with
aggressive histology and advanced disease.
Paraneoplastic syndromes are found in approximately
30% of patients with symptomatic RCCs. A few symptomatic
patients present with symptoms caused by metastatic
disease, such as bone pain or persistent cough.
Imaging
Computed tomography imaging, before and after intravenous
contrast, can verify the diagnosis and provide information on
the function and morphology of the contralateral kidney and
assess tumour extension, including extra-renal spread, venous
involvement, and enlargement of lymph nodes (LNs) and
adrenals.
Abdominal US and magnetic resonance imaging (MRI)
are supplements to CT. Contrast-enhanced US can be
helpful in specific cases (e.g., chronic renal failure with a
relative contraindication for iodinated or gadolinium-based

contrast media, complex cystic masses, and differential
diagnosis of peripheral vascular disorders such as infarction
and cortical necrosis).
Magnetic resonance imaging can be used in patients with
possible venous involvement, or allergy to intravenous
contrast. Chest CT is the most accurate for chest staging
and is recommended in the primary work–up of patients with
suspected RCC.
In patients with hereditary RCC who are worried about the
radiation exposure of frequent CT scans, MRI may be offered
as alternative for follow-up imaging.
Biopsy
Percutaneous renal tumour biopsies are used:
• to obtain histology of radiologically indeterminate renal
masses;
• to select patients with small renal masses for active
surveillance;
• to obtain histology before, or simultaneously with, ablative
treatments;
• to select the most suitable form of medical and surgical
strategy in the setting of metastatic disease.
In patients with any sign of impaired renal function, a renal

scan and total renal function evaluation using estimated
glomerular filtration rate should always be undertaken to
optimise the treatment decision.
Renal biopsy is not indicated for comorbid and frail
patients who can be considered only for conservative
management (watchful waiting) regardless of biopsy results.

Recommendations for the diagnostic Strength rating
assessment of renal cell cancer
Use multi-phasic contrast-enhanced Strong
computed tomography (CT) of abdomen
and chest for the diagnosis and staging of
renal tumours.
Use magnetic resonance imaging to better Weak
evaluate venous involvement, reduce
radiation or avoid intravenous CT contrast.
Use non-ionising modalities, mainly Weak
contrast enhanced ultrasound, for further
characterisation of small renal masses,
tumour thrombus and differentiation of
unclear renal masses.
Do not routinely use bone scan and/or Weak
positron-emission tomography (PET) CT
for staging of RCC.
Perform a renal tumour biopsy before Strong
ablative therapy and systemic therapy
without previous pathology.
Perform a percutaneous biopsy in select Weak
patients who are considered for active
surveillance.
Use a coaxial technique when performing Strong
a renal tumour biopsy.
Do not perform a renal tumour biopsy of Strong
cystic renal masses.
Use a core biopsy technique rather than Strong
fine needle aspiration for histological
characterisation for solid renal tumours.

Histological diagnosis
A variety of renal tumours exist, and about 15% are benign. All
kidney lesions require examination for malignant behaviour.
Histopathological classification
The new WHO/ISUP classification will replace the Fuhrman
nuclear grade system in due time but will need validation.
The three most common RCC subtypes, with genetic and

histological differences, are: clear cell RCC (80-90%), papillary
RCC (10-15%), and chromophobe RCC (4-5%). The various RCC
types have different clinical courses and responses to therapy.
Prognostic factors
In all RCC types, prognosis worsens with stage and
histopathological grade. Histological factors include tumour
grade, RCC subtype, sarcomatoid features, microvascular
invasion, tumour necrosis, and invasion of the perirenal fat
and collecting system. Clinical factors include performance
status (PS), local symptoms, cachexia, anaemia, platelet count,
neutrophil/lymphocyte ratio, C-reactive protein and albumin.

Use the current Tumour, Node, Metastasis Strong
classification system.
Use grading systems and classify RCC Strong
subtype.
Use prognostic systems in the metastatic Strong
setting.
In localised disease, use integrated Strong
prognostic systems or nomograms to
assess risk of recurrence.

Disease Management
Treatment of localised RCC
Localised renal cancers are best managed with partial
nephrectomy (PN) rather than radical nephrectomy (RN),
irrespective of the surgical approach. Partial nephrectomy is
unsuitable in some patients with localised RCC due to:
• locally advanced tumour growth;
• unfavourable tumour location;
• significant health deterioration.
If pre-operative imaging and intra-operative findings

are normal, routine adrenalectomy is not indicated.
Lymphadenectomy should be restricted to staging because
the survival benefit of extended LN dissection is unclear in
patients with localised disease. In patients who have RCCs
with tumour thrombus and no metastatic spread, prognosis is
improved after nephrectomy and complete thrombectomy.
Nephron-sparing surgery versus radical nephrectomy

Based on current available oncological and quality of life
outcomes, localised renal cancers are best managed by
nephron-sparing surgery (NSS) rather than RN, irrespective of
the surgical approach. Before routine nephrectomy, tumour
embolisation has no benefit. In patients unfit for surgery with
massive haematuria or flank pain, embolisation can be a
beneficial palliative approach.

Offer surgery to achieve cure in localised Strong
RCC.
Offer partial nephrectomy to patients with Strong
T1 tumours.

Do not perform ipsilateral adrenalectomy if Strong
there is no clinical evidence of invasion of
the adrenal gland.
Consider an extended lymph node Weak
dissection in patients with adverse clinical
features including a large diameter of the
primary tumour.
Offer embolisation in patients unfit for Weak
surgery presenting with massive
haematuria or flank pain.
Radical- and partial nephrectomy techniques
Summary of evidence LE
Laparoscopic RN has lower morbidity than open 1b
surgery.
Oncological outcomes for T1-T2a tumours are 2a
equivalent between laparoscopic and open RN.
Partial nephrectomy can be performed, either with an 2b
open, pure laparoscopic- or robot-assisted approach,
based on surgeon’s expertise and skills.
Partial nephrectomy is associated with a higher 3
percentage of positive surgical margins compared
with RN.

Offer laparoscopic radical nephrectomy (RN) Strong
to patients with T2 tumours and localised
masses not treatable by partial
nephrectomy.

Do not perform minimally invasive RN in Strong
patients with T1 tumours for whom a partial
nephrectomy is feasible by any approach,
including open.
Do not perform minimally invasive surgery Strong
if this approach may compromise
oncological, functional and perioperative
outcomes.
Alternatives to surgery
Surveillance
Elderly and comorbid patients with incidental small renal
masses have a low RCC-specific mortality and significant
competing-cause mortality. In selected patients with
advanced age and/or comorbidities, active surveillance (AS)
is appropriate to initially monitor small renal masses, followed,
if required, by treatment for progression. The concept of AS
differs from the concept of watchful waiting. Watchful waiting
is reserved for patients whose comorbidities contraindicate
any subsequent active treatment and who do not require
follow-up imaging, unless clinically indicated.
Cryoablation and radiofrequency ablation

Currently there are no data showing oncological benefit of
cryoablation or radiofrequency ablation (RFA) techniques over
PN.

Offer active surveillance, radiofrequency Weak
ablation and cryoablation to elderly and/or
comorbid patients with small renal masses.

Treatment of locally advanced RCC
Management of clinically positive lymph nodes (cN+)
In the presence of clinically positive LNs (cN+), LND is always
justified but the extent of LND is still controversial.
Low level data suggest that tumour thrombus in the
setting of non-metastatic disease should be excised.
Adjunctive procedures such as tumour embolisation or
inferior vena cava filter do not appear to offer any benefits in
the treatment of tumour thrombus.
In patients unfit for surgery, or with non-resectable
disease, embolisation can control symptoms, including visible
haematuria or flank pain. At present there is no evidence for
the use of adjuvant therapy following surgery.
Treatment of advanced/metastatic RCC

Management of RCC with venous tumour thrombus

In patients with clinically enlarged lymph Weak
nodes, perform lymph node dissection for
staging purposes or local control.
In case of venous involvement, remove the Strong
renal tumour and thrombus.
Cytoreductive nephrectomy
Tumour nephrectomy is curative only if all tumour deposits
are excised. This includes patients with the primary tumour
in place and single- or oligo-metastatic resectable disease.
For most patients with metastatic disease, cytoreductive
nephrectomy is palliative and systemic treatments are
necessary.

Cytoreductive nephrectomy combined with 1a
interferon-alpha (INF-α) improves survival in patients
with metastatic RCC and good performance status.
Deferred cytoreductive nephrectomy with presurgical 2b
sunitinib in intermediate-risk patients with clear-cell
metastatic RCC leads to a survival benefit in
secondary endpoint analysis and selects out patients
with inherent resistance to systemic therapy.
Cytoreductive nephrectomy for patients with 3
simultaneous complete resection of a single
metastasis or oligometastases may improve survival
and delay systemic therapy.
Patients with IMDC poor risk (≥ four risk factors) do 2b
not benefit.

Offer cytoreductive nephrectomy to Weak
favourable- and intermediate-risk patients
with metastatic RCC (mRCC).
Do not offer cytoreductive nephrectomy Weak
in IMDC poor-risk patients with ≥ four risk
factors.
Perform immediate cytoreductive Weak
nephrectomy in patients with
oligometastases when complete resection
can be achieved.
Offer deferred cytoreductive nephrectomy Weak
to intermediate-risk patients with clear-cell
mRCC who require systemic therapy with
sunitinib.
IMDC = The Metastatic Renal Cancer Database Consortium.

Local therapy of metastases in metastatic RCC (mRCC)
A systematic review of the local treatment of metastases from
RCC in any organ was undertaken. The heterogeneity of the
data will only allow for cautious recommendations.
All included studies were retrospective 3
non-randomised comparative studies, resulting in a
high risk of bias associated with non-randomisation,
attrition, and selective reporting.
With the exception of brain and possibly bone 3
metastases, metastasectomy remains by default the
only local treatment for most sites.
Retrospective comparative studies consistently point 3
towards a benefit of complete metastasectomy in
mRCC patients in terms of overall survival, cancer-
specific survival and delay of systemic therapy.
Radiotherapy to bone and brain metastases from RCC 3
can induce significant relief from local symptoms
(e.g. pain).

Offer local therapy for metastatic disease Weak
(including metastasectomy) to patients
with a favourable disease profile in whom
complete resection is achievable or when
local symptoms need to be controlled.
Offer stereotactic radiotherapy for clinically Weak
relevant bone or brain metastases for local
control and symptom relief.

Systemic therapy for advanced/metastatic RCC
Chemotherapy
In metastatic RCC, 5-fluorouracil combined with 1b
immunotherapy has equivalent efficacy to INF-α.
In metastatic RCC, chemotherapy is otherwise not 3
effective with the exception of gemcitabine and
doxorubicine in sarcomatoid and rapidly progressive
disease.
Recommendation Strength rating

Do not offer chemotherapy as first-line Strong
therapy in patients with clear-cell
metastatic RCC.
Immunotherapy
Interferon-α may only be effective in some patient subgroups,
including patients with clear-cell RCC (ccRCC), favourable-risk
criteria, and lung metastases only. Interleukin-2 (IL-2), vaccines
and targeted immunotherapy have no place in the standard
treatment of advanced/mRCC.
Immune checkpoint inhibition of programmed death receptor

(PD-1) and ligand (PD-L1) inhibition have been investigated
in mRCC. Randomised data support the use of nivolumab
(a PD-1 inhibitor) in vascular endothelial growth factor (VEGF)-
refractory disease. A combination of two immune checkpoint
inhibitors ipilimumab and nivolumab versus sunitinib in a
phase III study on metastatic RCC showed superior survival
for a combination of ipilimumab and nivolumab in
intermediate- and poor-risk patients.

Interferon-α monotherapy is inferior to VEGF-targeted 1b
therapy or mTOR inhibition in mRCC.
Interleukin (IL)-2 monotherapy may have an effect in 2a
selected cases (good PS, ccRCC, lung metastases only).
IL-2 has more side-effects than IFN-α. 2b
High-dose (HD)-IL-2 is associated with durable 1b
complete responses in a limited number of patients.
However, no clinical factors or biomarkers exist to
accurately predict a durable response in patients
treated with HD-IL-2.
Bevacizumab plus IFN-α is more effective than IFN-α 1b
in treatment-naïve, low-risk and intermediate-risk
ccRCC.
Vaccination therapy with tumour antigen 5T4 showed 1b
no survival benefit over first-line standard therapy.
Cytokine combinations, with or without additional 1b
chemotherapy, do not improve overall survival (OS)
compared with monotherapy.
Nivolumab leads to superior OS compared to 1b
everolimus in patients failing one or two lines of
VEGF-targeted therapy.
The combination of nivolumab and ipilimumab in 1b
treatment-naïve patients with clear-cell mRCC of
IMDC intermediate-and poor-risk leads to superior
survival compared to sunitinib.
The combination of nivolumab and ipilimumab in the 2b
intention to treat population of treatment-naïve
unselected patients with clear-cell mRCC leads to
superior survival compared to sunitinib.

Due to the exploratory nature of PD-L1 tumour 2b
expression, the small sample size, the lack of OS data
and the premature results in this subpopulation,
definitive conclusions cannot be drawn.
Nivolumab plus ipilimumab was associated with 15% 1b
grade 3-5 toxicity and 1.5% treatment-related deaths.

Use ipilimumab plus nivolumab in Strong
treatment-naïve patients with clear-cell
mRCC of IMDC intermediate and poor risk.
Offer nivolumab after one or two lines of Strong
VEGF-targeted therapy in mRCC.
Do not offer monotherapy with interferon-α Weak
or high-dose bolus interleukin-2 as first-line
therapy in mRCC.
Do not use bevacizumab plus INF-α in Weak
treatment-naïve clear-cell favourable- and
intermediate-risk RCC patients.
Do not use PD-L1 tumour expression as a Weak
predictive biomarker.
Administer nivolumab plus ipilimumab in Weak
centres with experience of immune
combination therapy and appropriate
supportive care within the context of a
multidisciplinary team.
Do not rechallange patients who stop Strong
nivolumab plus ipilimumab because of
toxicity with the same drugs in the future
without expert guidance and support from
a multidisciplinary team.
IMDC = The Metastatic Renal Cancer Database Consortium;
VEGF = vascular endothelial growth factor.

Targeted therapies
At present, several targeting drugs have been approved both
for the treatment of mRCC.
VEGF-targeted therapies increase progression-free 1b
survival (PFS) and/or OS as both first-line and second-
line treatments for patients with clear-cell mRCC.
Cabozantinib in intermediate-and poor-risk treatment- 1a
naïve clear-cell RCC leads to better response rates
and PFS but not OS when compared to sunitinib.
Tivozanib has recently been approved but the 3
evidence is still considered inferior over existing
choices.
Axitinib has proven efficacy and superiority in PFS as 1b
a second-line treatment after failure of cytokines and
VEGF-targeted therapy in comparison with sorafenib.
Sunitinib is more effective than IFN-α in treatment- 1b
naïve patients.
In treatment-naïve patients, bevacizumab in 1b
combination with INF-α has not been tested against
nivolumab plus ipilimumab and the evidence for
subsequent therapies is unclear.
Pazopanib is superior to placebo in both treatment- 1b
naïve mRCC patients and post-cytokine patients.
First-line pazopanib is not inferior to sunitinib in clear- 1b
cell mRCC patients.
Temsirolimus monotherapy prolongs OS compared to 1b
IFN-α in treatment-naïve poor-risk mRCC.
In treatment-naïve patients, temsirolimus has not 3
been tested against nivolumab plus ipilimumab and
the evidence for subsequent therapies is unclear.

Cabozantinib is superior to everolimus in terms of 1b
PFS and OS in patients after one or more lines of
VEGF-targeted therapy.
Everolimus prolongs PFS after VEGF-targeted therapy 1b
when compared to placebo or when the patient
cannot tolerate these therapies.
Sorafenib has broad activity in a spectrum of settings 4
in ccRCC patients previously treated with cytokine or
targeted therapies. It is inferior to axitinib in both
sunitinib or cytokine pre-treated patients.
Both mTOR inhibitors (everolimus and temsirolimus) 2a
and VEGF-targeted therapies (sunitinib or sorafenib)
have limited oncological efficacy in non-clear cell RCC.
There is a non-significant trend for improved
oncological outcomes for sunitinib, over everolimus.
Lenvatinib in combination with everolimus modestly 2a
improved PFS over everolimus alone.

Use sunitinib or pazopanib in treatment- Strong
naïve patients with clear-cell mRCC of
IMDC favourable risk.
Use cabozantinib in treatment-naïve Weak
patients with clear-cell mRCC of IMDC
intermediate and poor risk.
Do not use bevacizumab plus INF-α in Weak
treatment-naïve clear-cell favourable- and
intermediate-risk RCC patients.
Do not use tivozanib in treatment-naïve Weak
clear-cell mRCC patients.
Do not use temsirolimus in treatment-naïve Weak
clear-cell poor-risk RCC patients.

Use VEGF-TKIs in second-line in patients Weak
refractory to nivolumab plus ipilimumab.
Offer cabozantinib for ccRCC after one Strong
or two lines of VEGF-targeted therapy in
mRCC.
Offer axitinib, everolimus or lenvatinib plus Strong
everolimus to ccRCC patients who failed
VEGF-targeted therapy, and when
nivolumab or cabozantinib are not safe,
tolerable or available.
Sequence systemic therapy in treating Strong
mRCC.
Offer sunitinib as first-line therapy for Weak
non-clear cell mRCC.
Do not offer sorafenib as second-line Weak
treatment to patients with mRCC.
IMDC = The Metastatic Renal Cancer Database Consortium;
VEGF = vascular endothelial growth factor.

Figure 1: Updated EAU Guidelines recommendations for the
treatment of first-line clear-cell metastatic renal
cancer.
First-line therapy Second-line therapy Third-line therapy
IMDC favourable suninib or cabozannib or cabozannib or

risk disease pazopanib nivolumab nivolumab
cabozannib or cabozannib or an
ipilimumab/
VEGF-targeted alternave targeted
nivolumab
IMDC intermediate therapy therapy
and poor risk
disease cabozannib, VEGF targeted An alternave
suninib or therapy or targeted therapy or
pazopanib* nivolumab nivolumab
Boxed categories represent strong recommendaons
IMDC = The International Metastatic Renal Cell Carcinoma

Database Consortium; VEGF = vascular endothelial growth
factor.
*pazopanib for intermediate-risk disease only.
Recurrent RCC
Locally recurrent disease can occur either after nephrectomy,
PN, or after ablative therapy. After nephron-sparing treatment
approaches the recurrence may be intra-renal or regional, e.g.
venous tumour thrombi or retroperitoneal LN metastases.
Isolated local recurrence in the true renal fossa is rare.
Patients can benefit from a complete surgical resection of
local recurrent disease. In cases where complete surgical
removal is not feasible due to advanced tumour growth and
pain, palliative treatments including radiation treatment can
be considered.

Surveillance following surgery for RCC
The aim of surveillance is to detect either local recurrence or
metastatic disease while the patient is still surgically curable.
Surveillance after treatment for RCC allows the urologist to
identify:
• postoperative complications;
• renal function;
• local recurrence;
• recurrence in the contralateral kidney;
• development of metastases.
Depending on the availability of new effective treatments,

more intensive follow-up schedules may be required,
particularly as there is a higher local recurrence rate after
cryotherapy and RFA. At present there is no evidence-based
standard for the follow-up of patients with RCC, or for the
optimal duration of follow-up. An example of a surveillance
algorithm monitoring patients after treatment for RCC that
recognises not only the patient’s risk profile but also
treatment efficacy is provided in Table 2. For patients with
metastatic disease, individualised follow-up is indicated.

Table 2: Proposed surveillance schedule following treatment
for RCC, taking into account patient risk profile and
treatment efficacy
Risk profile Surveillance

6 mo 1 y 2y 3y >3y
Low US CT US CT CT once every 2 years;
counsel about recurrence
risk of ~10%
Intermediate CT CT CT CT CT once every 2 years
CT = computed tomography of chest and abdomen,
alternatively use magnetic resonance imaging for the
abdomen; US = ultrasound of abdomen, kidneys and renal
bed.
Summary of evidence and recommendations for surveillance

following RN or PN orablative therapies in RCC
Surveillance can detect local recurrence or metastatic 4
disease while the patient is still surgically curable.
After NSS, there is an increased risk of recurrence for 3
larger (> 7 cm) tumours, or when there is a positive
surgical margin.
Patients undergoing surveillance have a better overall 3
survival than patients not undergoing surveillance.
Repeated CT scans do not reduce renal function in 3
chronic kidney disease patients.

Base follow-up after RCC on the risk of Strong
recurrence.
Intensify follow-up in patients after NSS Weak
for tumours > 7 cm or in patients with a
positive surgical margin.
Base risk stratification on pre-existing Strong
classification systems such as the
University of California Los Angeles
integrated staging system integrated risk
assessment score
(http://urology.ucla.edu/body.cfm?id=443).

EAU Guidelines (ISBN: 978-94-92671-01-1), available to all members
of the European Association of Urology at their website:

EAU GUIDELINES ON TESTICULAR
CANCER
P. Albers (Chair), W. Albrecht, F. Algaba, C. Bokemeyer,

G. Cohn-Cedermark, K. Fizazi, A. Horwich,
M.P. Laguna (Vice-chair), N. Nicolai, J. Oldenburg
Guidelines Associates: J.L. Boormans, J. Mayor de Castro
Introduction
Compared with other types of cancer, testicular cancer is
relatively rare accounting for approximately 1-1.5% of all
cancers in men. Nowadays, testicular tumours show excellent
cure rates, mainly due to early diagnosis and their extreme
chemo- and radiosensitivity.
Staging and Classification

Staging
Postorchiectomy half-life kinetics of serum tumour markers
For an accurate staging the following steps are necessary
(see Table 1):
The persistence of elevated serum tumour markers after
orchiectomy may indicate the presence of disease, while their
normalisation does not necessarily mean absence of tumour.
Tumour markers should be assessed until they are normal, as
long as they follow their half-life kinetics and no metastases
are revealed. A chest computed tomography (CT) scan should
be routinely performed in patients diagnosed with non-
seminomatous germ cell tumours (NSGCT), because in up to
10% of cases, small subpleural nodes may be present that are
not visible radiologically.
Testicular Cancer 101

Table 1: Recommended tests for staging at diagnosis
Tests Recommendations Strength rating

Serum tumour - Alpha-fetoprotein Strong
markers - human chorionic
gonadotrophin
(hCG)
- Lactate
dehydrogenase
Abdominopelvic All patients Strong
computed
tomography (CT)
Chest CT All patients Strong
Testis ultrasound All patients Strong
(bilateral)
Bone scan or magnetic In case of Strong
resonance imaging symptoms
(MRI) columna
Brain scan (CT/MRI) In case of symptoms Strong
and patients with
metastatic disease
with multiple lung
metastases and/
or high beta-hCG
values.
Further investigations
Fertility investigations: Weak
• total testosterone
• luteinising hormone
• follicle-stimulating
hormone
• semen analysis
Discuss sperm banking with all men prior to Strong
starting treatment for testicular cancer.
102 Testicular Cancer

Staging system
The Tumour, Node, Metastasis (TNM 2017) staging system is
endorsed (Table 2).
Table 2: TNM classification for testicular cancer
pT - Primary Tumour1
pTX Primary tumour cannot be assessed (see note 1)
pT0 No evidence of primary tumour (e.g. histological scar
in testis)
pTIS Intratubular germ cell neoplasia (carcinoma in situ)
pT1 Tumour limited to testis and epididymis without
vascular/lymphatic invasion; tumour may invade
tunica albuginea but not tunica vaginalis*
pT2 Tumour limited to testis and epididymis with
vascular/lymphatic invasion, or tumour extending
through tunica lbuginea with involvement of tunica
vaginalis
pT3 Tumour invades spermatic cord with or without
vascular/lymphatic invasion
pT4 Tumour invades scrotum with or without vascular/
lymphatic invasion
N - Regional Lymph Nodes - Clinical
N1 Metastasis with a lymph node mass 2 cm or less in
greatest dimension and 5 or fewer positive nodes,
none more than 2 cm in greatest dimension
N2 Metastasis with a lymph node mass more than 2 cm
but not more than 5 cm in greatest dimension; or
more than 5 nodes positive, none more than 5 cm; or
evidence of extranodal extension of tumour

N3 Metastasis with a lymph node mass more than 5 cm
in greatest dimension
Pn - Regional Lymph Nodes - Pathological
pNX Regional lymph nodes cannot be assessed
pN0 No regional lymph node metastasis
pN1 Metastasis with a lymph node mass 2 cm or less in
greatest dimension and 5 or fewer positive nodes,
none more than 2 cm in greatest dimension
pN2 Metastasis with a lymph node mass more than 2 cm
but not more than 5 cm in greatest dimension; or
more than 5 nodes positive, none more than 5 cm; or
evidence or extranodal extension of tumour
pN3 Metastasis with a lymph node mass more than 5 cm
in greatest dimension
MX Distant metastasis cannot be assessed
M1a Non-regional lymph node(s) or lung metastasis
M1b Distant metastasis other than non-regional
lymph nodes and lung
S - Serum tumour markers
SX Serum marker studies not available or not performed
S0 Serum marker study levels within normal limits
LDH (U/l) hCG (mIU/mL) AFP (ng/mL)
S1 < 1.5 x N and < 5,000 and < 1,000
S2 1.5-10 x N or 5,000-50,000 or 1,000-10,000
S3 > 10 x N or > 50,000 or > 10,000
N indicates the upper limit of normal for the LDH assay.

LDH = lactate dehydrogenase; hCG = human chorionic
gonadotrophin; AFP = alpha-fetoprotein.

1Exceptfor pTis and pT4, where radical orchidectomy is not
always necessary for classification purposes, the extent of
the primary tumour is classified after radical orchidectomy;
see pT. In other circumstances, TX is used if no radical
orchidectomy has been performed.
The International Germ Cell Cancer Collaborative Group

(IGCCCG) defined a prognostic factor-based staging system
for metastatic germ cell cancer that includes good and
intermediate prognosis seminoma and good, intermediate,
and poor prognosis NSGCT (Table 3).
Table 3: Prognostic-based staging system for metastatic germ

cell cancer (IGCCCG)*
Good-prognosis group
Non-seminoma (56% of All of the following criteria:
cases) • Testis/retro-peritoneal primary
5-year PFS 89% • No non-pulmonary visceral
5-year survival 92% metastases
• AFP < 1,000 ng/mL
• hCG < 5,000 IU/L (1,000 ng/mL)
• LDH < 1.5 x ULN
Seminoma (90% of cases) All of the following criteria:
5-year PFS 82% • Any primary site
5-year survival 86% • No non-pulmonary visceral
metastases
• Normal AFP
• Any hCG
• Any LDH

Intermediate-prognosis group
Non-seminoma (28% of Any of the following criteria:
cases) • Testis/retro-peritoneal primary
5-year PFS 75% • No non-pulmonary visceral
• AFP 1,000 - 10,000 ng/mL or
• hCG 5,000 - 50,000 IU/L or
• LDH 1.5 - 10 x ULN
Seminoma (10% of cases) All of the following criteria:
5-year PFS 67% • Any primary site
5-year survival 72% • Non-pulmonary visceral
metastases
• Normal AFP
• Any hCG
• Any LDH
Poor-prognosis group
Non-seminoma (16% of Any of the following criteria:
cases) • Mediastinal primary
5-year PFS 41% • Non-pulmonary visceral
• AFP > 10,000 ng/mL or
• hCG > 50,000 IU/L
(10,000 ng/mL) or
• LDH > 10 x ULN
Seminoma No patients classified as poor
prognosis
* Pre-chemotherapy serum tumour markers should be
assessed immediately prior to the administration of
chemotherapy (same day).
PFS = progression-free survival; AFP = alpha-fetoprotein;
hCG = human chorionic gonadotrophin; LDH = lactate
dehydrogenase.

Diagnostic evaluation
The diagnosis of testicular cancer is based on:
Clinical examination of the testis and general examination
to rule out enlarged nodes or abdominal masses. Ultrasound
(US) of both testes should be performed whenever a testicular
tumour is suspected. An additional US of the retroperitoneum
is recommended to screen for extensive retroperitoneal
metastasis. Ultrasound of both testes should also be
performed in patients with a retroperitoneal mass and/or
elevated tumour serum markers without a palpable scrotal
mass.
Serum tumour markers, both before, and five to seven days

after orchiectomy (AFP and hCG) and LDH. The latter is
mandatory in advanced tumours.
Inguinal exploration and orchiectomy with en bloc removal of

testis, tunica albuginea, and spermatic cord. If the diagnosis
is not clear, a testicular biopsy (tumour enucleation) is to be
taken for histopathological frozen section.
Organ-sparing surgery can be attempted in special cases

(bilateral tumour or solitary testes). Routine contralateral
biopsy for diagnosis of carcinoma in situ should be discussed
with the patient and is recommended in 'high-risk' patients
(testicular volume < 12 mL, a history of cryptorchidism and
age < 40 years).
Pathological examination of the testis

Following orchiectomy, the pathological examination of the
testis should include a number of investigations.
1. macroscopic features: side, testis size, maximum tumour
size, and macroscopic features of the epididymis,
spermatic cord, and tunica vaginalis;

2. sampling: a 1 cm2 section for every centimetre of maximum
tumour diameter, including normal macroscopic
parenchyma (if present), albuginea and epididymis, with
selection of suspected areas;
3. at least one proximal and one distal section of spermatic
cord plus any suspected area;
4. microscopic features and diagnosis: histological type
(specify individual components and estimate amount as
percentage) according to WHO 2004;
5. presence or absence of peri-tumoural venous and/or
lymphatic invasion;
6. presence or absence of albuginea, tunica vaginalis, rete
testis, epididymis or spermatic cord invasion; presence
or absence of germ cell neoplasia in situ (GCNIS) in non-
tumour parenchyma;
7. pT category according to TNM 2016;
8. immunohistochemical studies: in seminoma and mixed
germ cell tumour, AFP and hCG.
Diagnosis and treatment of testicular intraepithelial

neoplasia
Diagnosis and treatment of testicular intraepithelial
neoplasia (TIN) Biopsy should be offered to patients at high
risk for contralateral TIN (testicular volume < 12 mL, history
of cryptorchidism or poor spermatogenesis). If performed,
a double biopsy is preferred. In the case of TIN, local
radiotherapy is indicated following counselling on impaired
testosterone production and infertility.

Recommendations for the diagnosis and Strength rating
staging of testicular cancer
Perform testicular ultrasound in all patients Strong
with suspicion of testicular cancer.
Offer biopsy of the contralateral testis and Strong
discuss its consequences with patients at
high risk for contralateral germ cell
neoplasia in situ.
Perform orchiectomy and pathological Strong
examination of the testis to confirm the
diagnosis and to define the local extension
(pT category). In a life-threatening situation
due to extensive metastasis, start
chemotherapy before orchiectomy.
Perform serum determination of tumour Strong
markers (alpha-fetoprotein, human
chorionic gonadotrophin, and lactate
dehydrogenase), both before, and five to
seven days after orchiectomy, for staging
and prognostic reasons.
Assess the state of the retroperitoneal, Strong
mediastinal and supraclavicular nodes and
viscera in testicular cancer.
Advise patients with a familiar history of Strong
testis cancer, as well as their family
members, to perform regular testicular
self-examination.

Prognosis
Risk factors for occult metastatic disease in stage I

testicular cancer
For seminoma For non-seminoma
Pathological (for stage I)
Histopathological • Tumour size • Vascular/lymphatic
type (> 4 cm) or peri-tumoural
• Invasion of the invasion
rete testis • Proliferation rate
> 70%
• Percentage of
embryonal
carcinoma > 50%
Disease management
Recommendations for the treatment of Strength rating

stage I seminoma
Fully inform the patient about all available Strong
management options, including
surveillance or adjuvant chemotherapy
after orchiectomy, as well as treatment-
specific recurrence rates and acute and
long-term side effects.
Offer surveillance as a management option Strong
if facilities are available and the patient is
compliant.
Offer one course at area under curve (AUC) Strong
7, if carboplatin chemotherapy is
considered.
Do not perform adjuvant treatment in Strong
patients at very low risk (no risk factors).

Do not perform radiotherapy as adjuvant Strong
treatment.
Recommendations for the treatment Strength rating

of stage 1 non-seminomatous germ cell
tumour
Inform patients with stage 1 non- Strong
seminomatous germ cell tumour (NSGCT)
about all adjuvant treatment options after
orchiectomy (surveillance, adjuvant
chemotherapy, and retroperitoneal lymph
node dissection [RPLND]) including
treatment-specific recurrence rates as well
as acute and long-term side effects.
In patients with stage 1 NSGCT, offer Strong
surveillance or risk-adapted treatment
based on vascular invasion (see below).
If patients are not willing to undergo Strong
surveillance, offer one course of cisplatin,
etoposide, bleomycin (BEP) as an adjuvant
treatment alternative since it has proven to
be superior to RPLND in terms of
recurrence rates.
In patients with marker-positive recurrent Strong
and/or progressing lesion during
surveillance, perform salvage treatment
consisting of three or four courses of BEP
chemotherapy according to the
International Germ Cell Cancer
Collaborative Group classification, followed
by post-chemotherapy RPLND, if necessary.

Recommendations for risk-adapted Strength rating
treatment for clinical stage 1 based on
vascular invasion
Stage IA (pT1, no vascular invasion): low risk
Offer surveillance if the patient is willing Strong
and able to comply.
In low-risk patients not willing (or Strong
unsuitable) to undergo surveillance, offer
adjuvant chemotherapy with one course of
cisplatin, etoposide, bleomycin (BEP).
Stage IB (pT2-pT4): high risk
Offer primary chemotherapy with one Strong
course of BEP, or surveillance.
Inform patients having adjuvant Strong
chemotherapy about the advantages and
disadvantages of one vs. two cycles of BEP.
Offer surveillance to patients not willing to Strong
undergo adjuvant chemotherapy.
Offer nerve-sparing retroperitoneal lymph Strong
node dissection to highly selected patients
only; those with contraindication to
adjuvant chemotherapy and unwilling to
accept surveillance.

Figure 1: Treatment options in patients with seminoma
clinical stage IIA and B
Clinical stage IIA Clinical stage IIB
either or either or
Radiotherapy Chemotherapy Chemotherapy Radiotherapy

2 Gy x 15 to a 3 x BEP or 4 x EP 3 x BEP or 4 x EP 2 Gy x 15 to a target
target dose of if if dose of 30 Gy
30 Gy to contraindications contraindications to para-aortic and
para-aortic to Bleomycin to Bleomycin ipsilateral iliac field
and ipsilateral and an additional
iliac field boost to the
enlarged lymph
nodes of
2 Gy x 3 to 6 Gy.
Follow-up Follow-up
Residual tumour to be followed
BEP = cisplatin, etoposide, bleomycin; EP = etoposide and

cisplatin.

metastatic germ cell tumours
Treat low volume non-seminomatous Strong
germ cell tumour (NSGCT) stage IIA/B
with elevated markers like ‘good- or
intermediate-prognosis’ advanced NSGCT,
with three or four cycles of cisplatin,
etoposide, bleomycin (BEP).

In stage IIA/B NSGCT without marker Strong
elevation, exclude marker negative
embryonal carcinoma by obtaining
histology by either retroperitoneal lymph
node dissection (RPLND) or biopsy. If not
possible, repeat staging after six weeks of
surveillance before making a final decision
on further treatment.
In metastatic NSGCT with an intermediate Strong
prognosis, treat with four courses of
standard BEP.
In metastatic NSGCT with a poor prognosis, Strong
treat with one cycle of BEP, or cisplatin,
etoposide and ifosfamide (PEI) in case of
poor lung function, followed by tumour
marker assessment after three weeks.
In case of a favourable marker decline,
continue BEP (or PEI) up to a total of four
cycles. In case of an unfavourable decline,
initiate chemotherapy intensification.
Perform surgical resection of residual Strong
masses after chemotherapy in NSGCT in
the case of visible residual masses and
when serum levels of tumour markers are
normal or normalising.
In CS IIA seminoma, offer radiotherapy or Strong
chemotherapy and inform the patient of
possible undesirable long-term side effects
of both management options.
Initially offer chemotherapy in seminoma Strong
stage CS IIB (BEP x 3 or EP x 4, in good
prognosis) as an alternative to radiotherapy.

Treat seminoma stage IIC and higher, with Strong
primary chemotherapy according to the
same principles used for NSGCT.
Relapse after chemotherapy

The treatment of relapsed GCT after chemotherapy is typically
salvage chemotherapy. For patients at first relapse with
good prognostic features (initial achievement of CR/PRM-
and gonadal primary tumour) four cycles of standard-dose
salvage chemotherapy are proposed. For patients with poor
prognostic factors (extragonadal primary and/or incomplete
response to first-line chemotherapy) and for all patients with
subsequent (> first) relapse, high-dose chemotherapy with
autologous stem cell support is recommended.
Follow-up
The primary aim of follow-up in the first five years is the timely
diagnosis of recurrent disease in order to be able to treat the
patient with curative intent with the least aggressive therapy.
a) Interval between examinations and duration of follow-up
should be consistent with the time of maximal risk of
recurrence;
b) Tests should be directed at the most likely sites of
recurrence and have a good accuracy;
c) The increased risk of second malignancy (in the primary
site and in other tissues that may have been exposed to
the same carcinogens, or in which there is epidemiological
evidence of increased risk) should also guide the selection
of tests;
d) Non-malignant complications of therapy must also be
considered.

Table 4: Recommended minimal follow-up for seminoma
stage I on active surveillance or after adjuvant
treatment (carboplatin or radiotherapy)
Modality Year Year Year Years After 5

1 2 3 4 & 5 years
Tumour markers 2 times 2 times 2 times once Further
± doctor visit management
Chest X-ray - - - - according to
survivorship
Abdominopelvic 2 times 2 times Once Once
care plan
computed tomography/ at 36 at 60
magnetic resonance months months
imaging
Table 5: Recommended minimal follow-up for non-seminoma

stage I on active surveillance
Modality Year Year Year Years After 5

1 2 3 4&5 years
Tumour markers 4 4 times 2 times 1-2 times Further
± doctor visit times** management
Chest X-ray 2 times 2 times Once, in At 60 according to
case of months survivorship
LVI+ if LVI+ care plan
Abdominopelvic 2 times At 24 Once Once

computed months at 36 at 60
tomography/magnetic *** months* months*
resonance imaging
*Recommended by 50% of the consensus group members.
**In case of high risk (LVI+) a minority of the consensus group
members recommended six times.
***In case of high risk (LVI+) a majority of the consensus group
members recommended an additional CT at eighteen
months.

Table 6: Recommended minimal follow up after adjuvant
treatment or complete remission for advanced
disease (excluded: poor prognosis and no remission)
Modality Year Year Year Years After

1 2 3 4 & 5 5 years
Tumour markers 4 times 4 times 2 times 2 times Further
± doctor visit management
Chest X-ray 1-2 Once Once Once according to
times survivorship
care plan**
Abdominopelvic 1-2 At 24 Once Once
computed tomography/ times months at 36 at 60
magnetic resonance months months
imaging
Thorax CT * * * *
*Same time points as abdomino-pelvic CT/MRI in case of
pulmonary metastases at diagnosis.
**In case of teratoma in resected residual disease: the patient
should remain with the uro-oncologist.
Quality of life and long-term toxicities after cure

Patients diagnosed with TC are usually between 18 and 40
years at diagnosis and life expectancy after cure extends over
several decades. Before any treatment is planned, patients
should be informed of common long-term toxicities.
During follow-up, patients should be screened and treated
for known risk factors such as high blood pressure,
hyperlipidaemia and testosterone deficiency. When follow up
by the clinical expert is discontinued, a written cancer
survivorship plan addressing late toxic effects, lifestyle
recommendations, recurrence risk, and cancer-specific
follow-up might be helpful.

Testicular Stromal Tumours
Testicular stromal tumours are rare, however, Leydig cell and
Sertoli cell tumours are of clinical relevance.
Leydig cell tumours

Approximately 10% of Leydig tumours are malignant
presenting the following features:
• large size (> 5 cm);
• cytologic atypia and DNA aneuploidy;
• increased mitotic activity and increased MIB-1 expression;
• necrosis;
• vascular invasion infiltrative margins;
• extension beyond the testicular parenchyma.
The tumour presents as a painless enlarged testis or as an

incidental US finding accompanied in up to 80% of cases by
hormonal disorders. Serum tumour markers are negative and
approximately 30% of patients present with gynaecomastia.
These tumours are often treated by inguinal orchiectomy
because they are misinterpreted as germ cell tumours. In
patients with symptoms of gynaecomastia or hormonal
disorders or typical imaging on US, until final histology is
available, a partial orchiectomy (+ frozen section) should be
considered. In the case of histological signs of malignancy,
orchiectomy and RPLND are the treatment of choice.
Sertoli cell tumours

Sertoli cell tumours are malignant in 10-22% of cases.
Morphological signs of malignancy are:
• large size (> 5 cm);
• pleomorphic nuclei with nucleoli;
• increased mitotic activity;
• necrosis and vascular invasion.

They present either as an enlarged testis or as incidental US
finding. Hormonal disorders are infrequent and serum tumour
markers are negative. Ultrasonographically, they generally
appear as hypoechoic and cannot be safely distinguished from
germ-cell tumour except for the subtype large cell calcifying
form which is usually associated with genetic syndromes
(Carney’s complex, Peutz-Jeghers syndrome). Sertoli cell
tumours are often interpreted as germ-cell tumours and an
orchiectomy is performed.
Organ-sparing surgery should be considered (with
caution) but, in the case of histological signs of malignancy,
orchiectomy and RPLND are the treatment of choice.
Conclusions
Most testis tumours are diagnosed at an early stage. Staging
is the cornerstone.
Following orchiectomy, excellent cure rates are achieved
for those early stages irrespective of the treatment policy
adopted, although pattern and relapse rates are closely linked
to the treatment modality chosen. In metastatic disease a
multidisciplinary therapeutic approach offers an acceptable
survival. Follow-up schedules should be tailored to initial
staging and treatment.

EAU Guidelines (978-94-92671-01-1), available to all members
of the European Association of Urology at their website:

EAU GUIDELINES ON PENILE CANCER
O.W. Hakenberg (Chair), E. Compérat, S. Minhas,

A. Necchi, C. Protzel, N. Watkin (Vice-chair)
Guidelines Associate: R. Robinson
Introduction and epidemiology

The incidence of penile cancer increases with age, peaking
during the sixth decade of life. However, the disease does
occur in younger men. There are significant geographical
variations within Europe as well as worldwide. Penile cancer
is common in regions with a high prevalence of human
Papilloma virus (HPV), which may account for the global
incidence variation, as the worldwide HPV prevalence varies
considerably. There is at present no recommendation for the
use of HPV vaccination in boys.
Risk factors
Recognised aetiological and epidemiological risk factors for
penile cancer are:
120 Penile Cancer

Risk factors Relevance
Phimosis Odds ratio 11-16 vs. no
phimosis
Chronic penile inflammation Risk
(balanoposthitis related to
phimosis), lichen sclerosus
Sporalene and ultraviolet A Incidence rate ratio 9.51 with
phototherapy for various > 250 treatments
dermatological conditions
such as psoriasis
Smoking Five-fold increased risk (95%
Confidence interval: 2.0-10.1)
vs. non-smokers
HPV infection, condylomata 22.4% in verrucous
acuminata squamous cell carcinoma
36-66.3% in basaloid-warty
Rural areas, low
socio-economic status,
unmarried
Multiple sexual partners, Three to five-fold increased
early age of first intercourse risk of penile cancer
Pathology
Different variants of squamous cell carcinoma (SCC) accounts
for more than 95% of cases of malignant penile disease.
Table 1 lists premalignant lesions and Table 2 lists the
pathological subtypes of penile carcinomas.
Penile Cancer 121

Table 1: Premalignant penile lesions (precursor lesions)
Lesions sporadically associated with squamous cell
carcinoma (SCC) of the penis:
• Bowenoid papulosis of the penis (HPV related)
• Lichen sclerosus
Premalignant lesions (up to one-third transform to invasive
SCC):
• Penile intraepithelial lesions
• Giant condylomata (Buschke-Löwenstein)
• Bowen’s disease
• Paget’s disease (intradermal ADK)
Table 2: Histological subtypes of penile carcinomas, their

frequency and outcome
Subtype Frequency Prognosis
(% of cases)
Common 48-65 Depends on location,
squamous cell stage and grade
carcinoma (SCC)
Basaloid carcinoma 4-10 Poor prognosis,
frequently early inguinal
nodal metastasis
Warty carcinoma 7-10 Good prognosis,
metastasis rare
Verrucous 3-8 Good prognosis, no
carcinoma metastasis
Papillary carcinoma 5-15 Good prognosis,
metastasis rare
Sarcomatoid 1-3 Very poor prognosis,
carcinoma early vascular metastasis
Mixed carcinoma 9-10 Heterogeneous group
122 Penile Cancer

Pseudohyperplastic < 1 Foreskin, related to
carcinoma lichen sclerosis, good
prognosis, metastasis
not reported
Carcinoma <1 Variant of verrucous
cuniculatum carcinoma, good
prognosis, metastasis
not reported
Pseudoglandular <1 High-grade carcinoma,
carcinoma early metastasis, poor
prognosis
Warty-basaloid 9-14 Poor prognosis, high
carcinoma metastatic potential
(higher than in warty,
lower than in basaloid
SCC)
Adenosquamous <1 Central and peri-
carcinoma meatal glans, high-
grade carcinoma, high
metastatic potential but
low mortality
Mucoepidermoid <1 Highly aggressive, poor
carcinoma prognosis
Clear cell variant of 1-2 Exceedingly rare,
penile carcinoma associated with
human papilloma
virus, aggressive,
early metastasis, poor
prognosis, outcome
is lesion-dependent,
frequent lymphatic
metastasis
Penile Cancer 123

Biopsy
Doubtful penile lesions should be biopsied and histological
verification obtained before local treatment. Histological
confirmation is necessary to guide management when:
• there is doubt about the exact nature of the lesion
(e.g. carcinoma in situ, metastasis or melanoma);
• treatment with topical agents, radiotherapy or laser surgery
is planned.
Recommendations for the pathological Strength rating

assessment of tumour specimens
The pathological evaluation of penile Strong
carcinoma specimens must include an
assessment of the HPV status.
carcinoma specimens must include a
diagnosis of the squamous cell carcinoma
subtype.
carcinoma surgical specimens must
include an assessment of surgical margins
including the width of the surgical margin.
Staging and classification systems

The 2016 UICC, Tumour Node Metastasis (TNM) classification
should be used for staging and classification (Table 3). The
T1 category is stratified into two prognostically different
risk groups. The classification T2 denotes invasion of
the corpus spongiosum and T3 invasion of the corpora
cavernosa, recognising that these two invasion patterns differ
prognostically. The current pN1 group consists of one or two
inguinal lymph node metastases, pN2 is more than two uni- or
bilateral metastatic nodes, and pN3 any pelvic nodes, uni- or
bilateral and any extranodal extension.
124 Penile Cancer

Table 3: 2016 TNM clinical and pathological classification of
penile cancer
Clinical classification
T - Primary tumour
Tis Carcinoma in situ
Ta Non-invasive verrucous carcinoma*
T1a Tumour invades subepithelial connective tissue
without lymphovascular invasion and is not
poorly differentiated
T1b Tumour invades subepithelial connective tissue
with lymphovascular invasion or is poorly
differentiated
T2 Tumour invades corpus spongiosum with or without
invasion of the urethra
T3 Tumour invades corpus cavernosum with or without
invasion of the urethra
T4 Tumour invades other adjacent structures
N - Regional lymph nodes
N0 No palpable or visibly enlarged inguinal lymph nodes
N1 Palpable mobile unilateral inguinal lymph node
N2 Palpable mobile multiple or bilateral inguinal lymph
nodes
N3 Fixed inguinal nodal mass or pelvic lymphadenopathy,
unilateral or bilateral
M - Distant metastasis
Penile Cancer 125

Pathological classification
The pT categories correspond to the clinical T categories
The pN categories are based upon biopsy or surgical excision
pN - Regional Lymph Nodes
pNX Regional lymph nodes cannot be assessed
pN0 No regional lymph node metastasis
pN1 Metastasis in one or two inguinal lymph nodes
pN2 Metastasis in more than two unilateral inguinal nodes
or bilateral inguinal lymph nodes
pN3 Metastasis in pelvic lymph node(s), unilateral or
bilateral or extranodal extension of regional lymph
node metastasis
pM - Distant Metastasis
pM1 Distant metastasis microscopically confirmed
G - Histopathological Grading
GX Grade of differentiation cannot be assessed
G1 Well differentiated
G2 Moderately differentiated
G3 Poorly differentiated
G4 Undifferentiated
*Verrucous carcinoma not associated with destructive
invasion.
Diagnostic evaluation and staging

Penile cancer can be cured in over 80% of all cases if
diagnosed early. Once metastatic spread has occurred, it is a
life-threatening disease with poor prognosis. Local treatment,
although potentially life-saving, can be mutilating and
devastating for the patient’s psychological well-being.
126 Penile Cancer

Physical Examination
Careful palpation of both groins for enlarged inguinal lymph
nodes must be part of the initial physical examination of
patients with penile cancer.
Imaging
• Ultrasound (US) can give information about infiltration of
the corpora.
• Magnetic resonance imaging (MRI) with an artificially
induced erection can help to exclude tumour invasion
of the corpora cavernosa if preservation of the penis is
planned.
• In case of non-palpable inguinal nodes, current imaging
techniques are not reliable in detecting micrometastases.
• A pelvic computed tomography (CT) scan can be used to
assess pelvic lymph nodeIn case of positive inguinal nodes,
CT of the abdomen and pelvis and a chest X-ray are
recommended; a thoracic CT will be more sensitive than
an X-ray.

staging of penile cancer
Primary tumour
Perform a physical examination, record Strong
morphology, extent and invasion of penile
structures.
Obtain a penile Doppler ultrasound or Weak
MRI with artificial erection in cases with
intended organ-sparing surgery.
Penile Cancer 127

Inguinal lymph nodes
Perform a physical examination of both Strong
groins, record the number, laterality and
characteristics of inguinal nodes and:
• If nodes are not palpable, offer invasive
lymph node staging in intermediate- and
high-risk patients;
• If nodes are palpable, stage with a pelvic
computed tomography (CT) or positron
emission tomography (PET)/CT.
Distant metastases
In N+ patients, obtain an abdominopelvic Strong
CT scan and chest X-ray/thoracic CT for
systemic staging. Alternatively, stage with
a PET/CT scan.
In patients with systemic disease or with
relevant symptoms, obtain a bone scan.
Disease management
Treatment of the primary penile cancer lesion aims to remove
the tumour completely while preserving as much of the penis
as possible without compromising radicality.
128 Penile Cancer

Recommendations for stage-dependent local treatment of
penile carcinoma
Primary tumour Use organ-preserving Strength
treatment whenever possible rating
Tis Topical treatment with Strong
5-fluorouracil or imiquimod
for superficial lesions with or
without photodynamic control.
Laser ablation with carbon
dioxide (CO2) or neodymium:
yttrium-aluminium-garnet
(Nd:YAG) laser.
Glans resurfacing.
Ta, T1a (G1, G2) Wide local excision with Strong
circumcision, CO2 or Nd:YAG
laser with circumcision.
Laser ablation with CO2 or
Nd:YAG laser.
Glans resurfacing.
Glansectomy with
reconstruction.
Radiotherapy for lesions
< 4 cm.
T1b (G3) and T2 Wide local excision plus Strong
reconstruction.
Glansectomy with
circumcision and
reconstruction.
Radiotherapy for lesions
< 4 cm in diameter.
T3 Partial amputation with Strong
reconstruction or radiotherapy
for lesions < 4 cm in diameter.
Penile Cancer 129

T3 with invasion Partial penectomy or total Strong
of the urethra penectomy with perineal
urethrostomy.
T4 Neoadjuvant chemotherapy Weak
followed by surgery in
responders or palliative
radiotherapy.
Local recurrence Salvage surgery with penis- Weak
sparing in small recurrences or
partial amputation.
Large or high-stage recurrence:
partial or total amputation.
Management of inguinal lymph nodes

The treatment of regional lymph nodes is crucial for the
survival of the patient. A surveillance strategy carries
considerable risk as regional lymph node recurrence
dramatically reduces the chance of long-term survival.
Invasive staging by modified inguinal lymphadenectomy or
dynamic sentinel node biopsy is recommended for penile
cancers pT1G1 and higher.
130 Penile Cancer

Recommendations for treatment strategies for nodal
metastases
Regional lymph Management of regional Strength
nodes lymph nodes is fundamental rating
in the treatment of penile
cancer
No palpable Tis, Ta G1, T1G1: surveillance. Strong
inguinal nodes > T1G2: invasive lymph Strong
(cN0) node staging by either
bilateral modified inguinal
lymphadenectomy or
dynamic sentinel node
biopsy.
Palpable inguinal Radical inguinal Strong
nodes (cN1/cN2) lymphadenectomy.
Fixed inguinal Neoadjuvant chemotherapy Weak
lymph nodes followed by radical inguinal
(cN3) lymphadenectomy in
responders.
Pelvic Ipsilateral pelvic Strong
Lymph nodes lymphadenectomy if two
or more inguinal nodes are
involved on one side (pN2)
or if extracapsular nodal
metastasis (pN3) reported.
Adjuvant In pN2/pN3 patients after Strong
chemotherapy radical lymphadenectomy.
Radiotherapy Not recommended for nodal Strong
disease except as a palliative
option.
Penile Cancer 131

Recommendations for chemotherapy in Strength rating
penile cancer patients
Offer patients with pN2-3 tumours Strong
adjuvant chemotherapy after radical
lymphadenectomy (three to four cycles
of cisplatin, a taxane and 5-fluorouracil or
ifosfamide).
Offer patients with non-resectable or Weak
recurrent lymph node metastases
neoadjuvant chemotherapy (four cycles of
a cisplatin- and taxane-based regimen)
followed by radical surgery.
Offer palliative chemotherapy to patients Weak
with systemic disease.
Follow-up
Follow-up after curative treatment in penile carcinoma, as in
any malignant disease, is important for two reasons:
• early detection of recurrence allows for potentially curative
treatment;
• the detection and management of treatment-related
complications.
Local recurrence does not significantly reduce long-term
survival if successfully treated, while inguinal nodal recurrence
leads to a drastic reduction in the probability of long-term
disease-specific survival.
132 Penile Cancer

Recommendations for follow-up in penile cancer
Interval of follow-up Examinations and investigations Minimum duration Strength
Years one to Years three of follow-up rating
two to five
Recommendations for follow-up of the primary tumour
Penile- Three months Six months Regular physician or self-examination. Five years Strong
preserving Repeat biopsy after topical or laser
treatment treatment for penile intraepithelial
neoplasia.
Amputation Three months One year Regular physician or self-examination. Five years Strong
Recommendations for follow-up of the inguinal lymph nodes
Surveillance Three months Six months Regular physician or self-examination. Five years Strong
pN0 at initial Three months One year Regular physician or self-examination. Five years Strong
treatment Ultrasound with fine-needle
aspiration biopsy optional.
pN+ at initial Three months Six months Regular physician or self-examination. Five years Strong
treatment Ultrasound with fine-needle
aspiration cytology optional,
computed tomography/magnetic
resonance imaging optional.
Penile Cancer 133

Quality of life
Overall, nearly 80% of penile cancer patients of all stages can
be cured. Partial penectomy has negative consequences for
the patients’ self-esteem and sexual function. Organ
preserving treatment allows for better quality of life and sexual
function and should be offered to all patients whenever
feasible. Referral to centres with experience is recommended
and psychological support is very important for penile cancer
patients.

EAU Guidelines (ISBN 978-94-92671-01-1), available to all members
of the European Association of Urology at their website,
134 Penile Cancer

EAU GUIDELINES ON NON-
NEUROGENIC MALE LUTS INCLUDING
BENIGN PROSTATIC OBSTRUCTION
S. Gravas (Chair), J.N. Cornu, M.J. Drake, M. Gacci, C. Gratzke,

T.R.W. Herrmann, S. Madersbacher, C. Mamoulakis,
K.A.O. Tikkinen
Guidelines Associates: M. Karavitakis, I. Kyriazis, S. Malde,
V. Sakkalis, R. Umbach
Introduction
The EAU Guidelines on Male Lower Urinary Tract Symptoms
(LUTS) is a symptom-orientated guideline that mainly reviews
LUTS secondary to benign prostatic obstruction (BPO),
detrusor overactivity/overactive bladder (OAB), or nocturnal
polyuria in men ≥ 40 years. The multifactorial aetiology of
LUTS is illustrated in Figure 1.
Non-neurogenic Male LUTS including benign prostatic obstruction 135

Figure 1: Causes of male lower urinary tract symptoms (LUTS)
Benign
prostatic
Detrusor obstruction
under- Others
activity
Overactive
bladder / Distal
detrusor ureteric
overactivity stone
Nocturnal Bladder
polyuria LUTS tumour
Chronic
pelvic pain Urethral
syndrome stricture
Neurogenic
Foreign
bladder
dysfunction Urinary body
tract
infection
The high prevalence and the underlying multifactorial patho-
physiology of male LUTS mean that an accurate assessment
of LUTS is critical to provide best evidence-based care. Clinical
assessment of LUTS aims to differentially diagnose and to
define the clinical profile. A practical algorithm has been
developed (Figure 2).
136 Non-neurogenic Male LUTS including benign prostatic obstruction

evaluation of male LUTS
Take a complete medical history from men Strong
with LUTS.
Use a validated symptom score Strong
questionnaire including bother and quality
of life assessment during the assessment
of male LUTS and for re-evaluation during
and/or after treatment.
Use a bladder diary to assess male LUTS Strong
with a prominent storage component or
nocturia.
Tell the patient to complete a bladder diary Strong
for the duration of at least three days.
Perform a physical examination including Strong
digital rectal examination in the
assessment of male LUTS.
Urinalysis and prostate-specific antigen (PSA)
Use urinalysis (by dipstick or urinary Strong
sediment) in the assessment of male LUTS.
Measure PSA if a diagnosis of prostate Strong
cancer will change management.
Measure PSA if it assists in the treatment Strong
and/or decision making process.
Renal function, post-void residual and uroflowmetry
Assess renal function if renal impairment Strong
is suspected based on history and clinical
examination, or in the presence of
hydronephrosis, or when considering
surgical treatment for male LUTS.
Measure post-void residual in the Weak

Perform uroflowmetry in the initial Weak
Perform uroflowmetry prior to medical or Strong
invasive treatment.
Imaging and urethrocystoscopy
Perform ultrasound of the upper urinary Weak
tract in men with LUTS.
Perform imaging of the prostate when Weak
considering medical treatment for male
LUTS, if it assists in the choice of the
appropriate drug.
Perform imaging of the prostate when Strong
considering surgical treatment.
Perform urethrocystoscopy in men with Weak
LUTS prior to minimally invasive/surgical
therapies if the findings may change
treatment.
Pressure-flow studies (PFS)
Perform PFS only in individual patients for Weak
specific indications prior to invasive treat-
ment or when evaluation of the underlying
pathophysiology of LUTS is warranted.
Perform PFS in men who have had previous Weak
unsuccessful (invasive) treatment for LUTS.
Perform PFS in men considering invasive Weak
treatment who cannot void > 150 mL.
Perform PFS when considering surgery in Weak
men with bothersome predominantly
voiding LUTS and Qmax > 10 mL/s.

Perform PFS when considering invasive Weak
therapy in men with bothersome,
predominantly voiding LUTS with a post-
void residual > 300 mL.
treatment in men with bothersome, pre-
dominantly voiding LUTS aged > 80 years.
treatment in men with bothersome, pre-
dominantly voiding LUTS aged < 50 years.
Non-invasive tests in diagnosing bladder outlet obstruction
Do not offer non-invasive tests, as an Strong
alternative to PFS, for diagnosing bladder
outlet obstruction in men.

Figure 2: Assessment algorithm of LUTS in men aged 40 years
or older
Male LUTS Manage according to
EAU mLUTS
treatment algorithm
History (+ sexual function) No

Symptom score questionnaire
Urinalysis
Physical examination
PSA (if diagnosis of PCa will change the
management – discuss with patient) Bothersome
Measurement of PVR symptoms
Yes
Abnormal DRE Significant PVR
Suspicion of
neurological disease
High PSA
Abnormal urinalysis FVC in cases of predominant
US of kidneys storage LUTS/nocturia
+/- Renal function US assessment of prostate
assessment Uroflowmetry
Evaluate according to
relevant guidelines or
clinical standard Benign conditions of
Medical treatment
according to treatment bladder and/or prostate
algorithm with baseline values
PLAN TREATMENT
Treat underlying
condition
(if any, otherwise Endoscopy (if test would alter the
return to initial choice of surgical modality)
assessment) Pressure-flow studies (see text for
specific indications)
Surgical treatment according

to treatment algorithm
DRE = digital-rectal examination; FVC = frequency volume

chart; LUTS = lower urinary tract symptoms;
PCa = prostate cancer; PSA = prostate specific antigen;
PVR = post-void residual; US = ultrasound.
Notice: Readers are strongly recommended to read the full

text that highlights the current position of each test in detail.

Disease Management
Conservative and pharmacological treatment
Watchful waiting is suitable for mild-to-moderate
uncomplicated LUTS. It includes education, re-assurance,
lifestyle advice, and periodic monitoring.
Recommendation for the conservative Strength rating

and pharmacological management of male
LUTS.
Conservative management
Offer men with mild/moderate symptoms, Strong
minimally bothered by their symptoms,
watchful waiting.
Offer men with LUTS lifestyle advice prior Strong
to, or concurrent with, treatment.
Pharmacological management
Offer α1-blockers to men with moderate-to- Strong
severe LUTS.
Use 5α-reductase inhibitors (5-ARIs) in men Strong
who have moderate-to-severe LUTS and an
increased risk of disease progression
(e.g. prostate volume > 40 mL).
Counsel patients about the onset of action Strong
(3-6 months) of 5-ARIs.
Use muscarinic receptor antagonists in Strong
men with moderate-to-severe LUTS who
mainly have bladder storage symptoms.
Do not use antimuscarinic overactive Weak
bladder medications in men with a post-
void residual (PVR) volume > 150 mL.
Use phosphodiesterase type 5 inhibitors in Strong
men with moderate-to-severe LUTS with or
without erectile dysfunction.

Use beta-3 agonists in men with moderate- Weak
to-severe LUTS who mainly have bladder
storage symptoms.
Offer combination treatment with an Strong
α1-blocker and a 5-ARI to men with
moderate-to-severe LUTS and an increased
risk of disease progression (e.g. prostate
volume > 40 mL).
Use combination treatment of a α1-blocker Strong
with a muscarinic receptor antagonist in
patients with moderate-to-severe LUTS
if relief of storage symptoms has been
insufficient with monotherapy with either
drug.
Do not prescribe combination treatment in Weak
men with a PVR volume > 150 mL.
Summary conservative and/or medical treatment

First choice of therapy is behavioural modification, with or
without pharmacological treatment. A flowchart illustrating
conservative and pharmacological treatment choices
according to evidence-based medicine and patients’ profiles
is provided in Figure 3.

Figure 3: Treatment algorithm of male LUTS using medical
and/or conservative treatment options.
Treatment decisions depend on results assessed during initial

evaluation. Note that patients’ preferences may result in
different treatment decisions.
Male LUTS
(without indications for surgery)
Bothersome
no symptoms? yes
Nocturnal
no polyuria yes
predominant
no Storage symptoms yes

predominant?
Prostate
no volume yes
> 40 mL?
Education + lifestyle Long-term

advice with or without no treatment?
α1-blocker/PDE5I
yes
Residual
storage
symptoms
Watchful Add muscarinic Education + Education + Education +

waiting receptor lifestyle advice lifestyle advice lifestyle advice
with or without antagonist/beta with or without with or without with or without
education + -3 agonist 5α-reductase muscarinic vasopressin
lifestyle advice inhibitor ± α1- receptor analogue
blocker/PDE5I antagonist/beta
-3 agonist
LUTS = lower urinary tract symptoms;

PDE5I = phosphodiesterase type 5 inhibitor.
Notice: Readers are strongly recommended to read the full text
that highlights the current position of each treatment in detail.
Surgical treatment
Prostate surgery is usually required when patients have
experienced recurrent or refractory urinary retention,
overflow incontinence, recurrent urinary tract infections,
bladder stones or diverticula, treatment-resistant macroscopic
haematuria due to BPH/BPE, or dilatation of the upper urinary
tract due to BPO, with or without renal insufficiency (absolute
operation indications, need for surgery). Surgery is usually
needed when patients have had insufficient relief of LUTS
or post-void residual after conservative or pharma-cological
treatments (relative operation indications).
Recommendations for surgical treatment Strength rating

of male LUTS
Offer transurethral incision of the prostate Strong
to surgically treat moderate-to-severe LUTS
in men with prostate size < 30 mL, without
a middle lobe.
Offer bipolar- or monopolar- transurethral Strong
resection of the prostate (TURP) to
surgically treat moderate-to-severe LUTS in
men with prostate size of 30-80 mL.
Offer plasma bipolar transurethral Strong
vaporisation of the prostate as an
alternative to TURP to surgically treat
moderate-to-severe LUTS in men with
prostate size of 30-80 mL.
Offer endoscopic enucleation of the Strong
prostate or open prostatectomy to treat
moderate-to-severe LUTS in men with
prostate size > 80 mL.

Offer open prostatectomy in the absence of Strong
endoscopic enucleation to treat moderate-
to-severe LUTS in men with prostate size
> 80 mL.
Laser treatments of the prostate
Offer laser enucleation of the prostate Strong
using holmium:yttrium-aluminum-garnet
laser (HoLEP) to men with moderate-to-
severe LUTS as an alternative to TURP or
open prostatectomy.
Offer 80 Watt 532-nm Kalium-Titanyl- Strong
phosphate (KTP) laser vaporisation of the
prostate to men with moderate-to-severe
LUTS as an alternative to TURP.
Offer 120 Watt 532-nm Lithium Borat (LBO) Strong
laser vaporisation of the prostate to men
with moderate-to-severe LUTS as an
alternative to TURP.
Offer 180 Watt 532-nm LBO laser Strong
vaporisation of the prostate to men with
moderate-to-severe LUTS as an alternative
to TURP.
Offer laser vaporisation of the prostate Weak
using 80 Watt KTP, 120 or 180 Watt LBO
for the treatment of patients receiving
antiplatelet or anticoagulant therapy with
a prostate volume < 80 mL.
Offer 120 Watt 980 nm diode laser Weak
vaporisation of the prostate to men with
moderate-to-severe LUTS as a comparable
alternative to TURP.

Offer 120 Watt 980 nm or 1,318 nm diode Weak
laser enucleation of the prostate to men
with moderate-to-severe LUTS as a
comparable alternative to TURP.
Offer laser enucleation of the prostate Weak
using Tm:YAG vapoenucleation (ThuVEP)
and Tm:YAG laser assisted anatomical
enucleation (ThuLEP) to men with
moderate-to-severe LUTS as alternatives
to TURP and HoLEP.
Offer ThuVEP to patients receiving Weak
anticoagulant or antiplatelet therapy.
Offer laser resection of the prostate using Strong
Tm:YAG laser (ThuVARP) as an alternative
to TURP.
Offer ThuVARP to patients receiving Weak
anticoagulant or antiplatelet therapy.
Prostatic stents and prostatic urethral lift
Offer prostatic stents as an alternative to Weak
catheterisation in men unfit for invasive
procedures requiring spinal or general
anaesthesia.
Offer Prostatic urethral lift (Urolift®) to Strong
men with LUTS interested in preserving
ejaculatory function, with prostates
< 70 mL and no middle lobe.
Novel interventions
Do not offer intraprostatic Botulinum toxin Strong
injection treatment to patients with male
LUTS.

Summary surgical treatment
The choice of the surgical technique depends on prostate
size, co-morbidities, ability to undergo anaesthesia, patient’s
preference/willingness to accept surgery-associated side
effects, availability of the surgical armamentarium, and
experience of the surgeon. Figure 4 illustrates surgical
treatment choices according to the patient’s profile.

Figure 4: Treatment algorithm of bothersome LUTS refractory
to conservative/medical treatment or in cases of
absolute operation indications.
The flowchart is stratified by the patient’s ability to have

anaesthesia, cardiovascular risk, and prostate size.
Male LUTS
with absolute indications for surgery or non-responders to medical treatment or those
who do not want medical treatment but request active treatment
High-risk
low high
patients?
Can have
yes surgery under no
anaesthesia?
Can stop
yes no
anticoagulation/
antiplatelet therapy
Prostate
< 30 mL volume > 80 mL
30 – 80 mL
TUIP (1) TURP (1) Open Laser TUMT

TURP Laser prostatectomy (1) vaporisation (1) TUNA
enucleation HoLEP (1) Laser PU lift
Bipolar Bipolar enucleation Stent
enucleation enucleation (1)
Laser Laser
vaporisation vaporisation
PU lift Thulium
TUMT enucleation
TUNA TURP
(1) Current standard/first choice. The alternative treatments are presented in alphabetical order.
Notice: Readers are strongly recommended to read the full text that highlights the current
position of each treatment in detail.

Laser vaporisation includes GreenLight, thulium, and diode
laser vaporisation; Laser enucleation includes holmium and
thulium laser enucleation.
HoLEP = holmium laser enucleation; TUIP = transurethral
incision of the prostate; TUMT = transurethral microwave
therapy; TUNA = transurethral needle ablation; TURP =
transurethral resection of the prostate.
Management of Nocturia in Men with LUTS
Diagnostic assessment
Evaluation is outlined in Figure 5.

Figure 5: Evaluation of nocturia in non-neurogenic male LUTS
• History (+ sexual function)

• Symptom Score Questionnaire
• Physical Examination
• Urinalysis Bothersome Nocturia
• PSA (if diagnosis of PCa will change
the management – discuss with patient)
• Measurement of PVR
yes no
Significant PVR
• US assessment of prostate
• Uroflowmetry
• US of kidneys +/- renal
function assessment
• FVC with predominant storage LUTS
• Abnormal DRE, high PSA Mixed features

• Haematuria Polyuria/ LUTS
• Chronic pelvic pain NP
Evaluate according to
relevant guidelines or
clinical standard
Medical Conditions/Sleep Nocturia with LUTS in
disorders Care Pathway benign LUT conditions
Treat underlying condition Behavioural and drug NP Behavioural and drug

or sleep disorder treatment LUTS treatment
Offer shared care LUTS Algorithm
Interventional LUTS
treatment
(Indirect MoA for
nocturia)
Assessment must establish whether the patient has polyuria,

LUTS, sleep disorder or a combination. Therapy may be driven
by the bother it causes, but non-bothersome nocturia may
warrant assessment of a frequency volume chart (FVC),
(indicated by the dotted line), depending on history and
clinical examination since potential presence of a serious
underlying medical condition must be considered.
DRE = digital rectal examination; NP = nocturnal polyuria;
MoA = mechanism of action; PVR = post-void residual;
PSA = prostate-specific antigen; US = ultrasound.

Medical conditions and sleep disorders shared care pathway
Figure 6: Shared care pathway for nocturia, highlighting the

need to manage potentially complex patients using
relevant expertise for the causative factors.
UROLOGICAL CONTRIBUTION SHARED CARE MEDICAL CONTRIBUTION
Diagnosis of LUTD Diagnosis of conditions causing NP
• Urological/LUTS evaluation • Evaluate patient’s known conditions
• Nocturia symptom scores • Screening for sleep disorders
• Bladder diary • Screening for potential causes of polyuria*
Conservative management Conservative management Management

Behavioural therapy • Initiation of therapy for new diagnosis
• Fluid/sleep habits advice • Antidiuretic • Optimised therapy of known conditions
• Drugs for storage LUTS • Diuretics
• (Drugs for voiding LUTS) • Drugs to aid sleep
* Potential causes of polyuria
• ISC/catherisation
NEPHROLOGICAL DISEASE
• Tubular dysfunction
• Global renal dysfunction
Interventional therapy CARDIOVASCULAR DISEASE
• Therapy of refractory • Cardiac disease
storage LUTS • Vascular disease
• Therapy of refractory ENDOCRINE DISEASE
• Diabetes insipidus/mellitus
voiding LUTS
• Hormones affecting diuresis/natriuresis
NEUROLOGICAL DISEASE
• Pituitary and renal innervation
• Autonomic dysfunction
RESPIRATORY DISEASE
• Obstructive sleep apnoea
BIOCHEMICAL
• Altered blood oncotic pressure

Recommendations for treatment of Strength rating
nocturia
Treat underlying causes of nocturia, in- Weak
cluding behavioural, systemic condition(s),
sleep disorders, lower urinary tract
dysfunction, or a combination of factors.
Discuss behavioural changes with the Weak
patient to reduce nocturnal urine volume
and episodes of nocturia, and improve
sleep quality.
Offer desmopressin to decrease nocturia Strong
due to nocturnal polyuria in men < 65.
Screen for hyponatremia at baseline, during
dose titration and during treatment.
Offer α1-adrenergic antagonists for treating Weak
nocturia in men who have nocturia
associated with LUTS.
Offer antimuscarinic drugs for treating Weak
associated with overactive bladder.
Offer 5α-reductase inhibitors for treating Weak
associated with LUTS and an enlarged
prostate (> 40 mL).
Do not offer phosphodiesterase type 5 Weak
inhibitors for the treatment of nocturia.
Follow-up
Recommended follow-up strategy:
• Patients managed with watchful waiting should be
reviewed at six months and then annually, provided
symptoms do not deteriorate or absolute indications
develop for surgical treatment.
• Patients receiving α1-blockers, muscarinic receptor

antagonists, beta-3 agonists, phospodiesterase 5 inhibitors,
or a combination should be reviewed four to six weeks
after drug initiation. If patients gain symptomatic relief,
without troublesome side effects, drug therapy may be
continued. Patients should be reviewed at six months and
then annually, provided symptoms do not deteriorate or
absolute indications develop for surgical treatment.
• Patients receiving 5α-reductase inhibitor should be
reviewed after twelve weeks and six months to determine
their response and adverse events.
• Patients receiving desmopressin: serum sodium
concentration should be measured at day three and seven
and after one month and, if serum sodium concentration
has remained normal, every three months subsequently;
the follow-up sequence should be restarted after dose
escalation.
• Patients after prostate surgery should be reviewed four
to six weeks after catheter removal to evaluate treatment
response and side effects. If patients have symptomatic
relief and there are no side effects, further assessment is
not necessary.

Follow-up all patients who receive Weak
conservative, medical or surgical
management.
Define follow-up intervals and examinations Weak
according to the specific treatment.
Readers are strongly recommended to read the full version of

the Guidelines where the efficacy, safety and considerations
for each treatment are presented.

EAU Guidelines (ISBN 978-94-92671-01-1) available to all members
http://www.uroweb.org/guidelines.

EAU GUIDELINES ON URINARY
INCONTINENCE
F.C. Burkhard (Chair), J.L.H.R. Bosch, F. Cruz, G.E. Lemack,

A.K. Nambiar, N. Thiruchelvam, A. Tubaro
Guidelines Associates: D. Ambühl, D. Bedretdinova, F. Farag,
R. Lombardo, M.P. Schneider
Introduction
This pocket version aims to synthesise the important
clinical messages described in the full text and is presented
as a series of ‘action based recommendations’ with a strength
rating.
History and physical examination
The history should include details of the type, timing and
severity of urinary incontinence (UI), associated voiding and
other urinary symptoms. The history should allow UI to be
categorised into stress urinary incontinence (SUI), urgency
urinary incontinence (UUI) or mixed urinary incontinence (MUI).
It should also identify patients who need rapid referral
to an appropriate specialist. These include patients with
associated pain, haematuria, a history of recurrent urinary
tract infection (UTI), pelvic surgery (particularly prostate
surgery) or radiotherapy, constant leakage suggesting a fistula,
voiding difficulty or suspected neurological disease. The patient
should also be asked about other ill health and for the details
of current medications, as these may impact on symptoms of
UI.
Urinary Incontinence 155

Questionnaires

Use a validated and appropriate Strong
questionnaire when standardised
assessment is required.
Voiding diaries

Ask patients with UI to complete a voiding Strong
diary.
Use a diary duration of at least three days. Strong
Urinalysis and urinary tract infection

Perform urinalysis as a part of the initial Strong
assessment of a patient with UI.
If a symptomatic urinary tract infection is Strong
present with UI, reassess the patient after
treatment.
Do not routinely treat asymptomatic Strong
bacteriuria in elderly patients to improve UI.
Post-voiding residual volume

When measuring post-void residual (PVR) Strong
urine volume, use ultrasound.
Measure (PVR) in patients with UI who have Strong
voiding symptoms.
156 Urinary Incontinence

Measure (PVR) when assessing patients Strong
with complicated UI.
Monitor PVR in patients receiving Strong
treatments that may cause or worsen
voiding dysfunction, including surgery for
SUI.
Urodynamics

(NB: Concerning only neurologically intact adults with UI)
When performing urodynamics in patients Strong
with UI adhere to ‘Good Urodynamic
Practice’ standards as described by the
International Continence Society:
• attempt to replicate the patient’s
symptoms;
• check recordings for quality control;
• interpret results in the context of the
clinical problem;
• remember there may be physiological
variability within the same individual.
Do not routinely carry out urodynamics Strong
when offering treatment for uncomplicated
SUI.
Perform urodynamics if the findings may Weak
change the choice of invasive treatment.
Do not use urethral pressure profilometry Strong
or leak point pressure to grade severity of
incontinence.

Pad testing

Use a pad test of standardised duration and Strong
activity protocol.
Use a pad test when quantification of UI is Weak
required.
Imaging

Do not routinely carry out imaging of the Strong
upper or lower urinary tract as part of the
assessment of UI.
Disease Management
Conservative management
In clinical practice, it is a convention that non-surgical
therapies are tried first because they usually carry the least
risk of harm. Conventional medical practice encourages the
use of simple, relatively harmless, interventions before
resorting to those associated with higher risks.
Simple medical interventions

Correction of underlying disease/cognitive impairment
Urinary incontinence, especially in the elderly, has been
associated with multiple comorbid conditions including:
• cardiac failure;
• chronic renal failure;
• diabetes;
• chronic obstructive pulmonary disease;
• neurological disease including stroke and multiple
sclerosis;
• general cognitive impairment;
• sleep disturbances, e.g. sleep apnoea;

• depression;
• metabolic syndrome.
Adjustment of medication
Although changing drug regimens for underlying disease may
be considered as a possible early intervention for UI, there is
very little evidence of benefit. There is also a risk that stopping
or altering medication may result in more harm than benefit.

Take a drug history from all patients with UI. Strong
Review any new medication associated Weak
with the development or worsening of UI.
Constipation
Studies have shown strong associations between
constipation and UI. Constipation can be improved by
behavioural, physical and medical treatments.

Advise adults with UI who also suffer from Strong
constipation about bowel management, in
line with good medical practice.
Containment (pads etc.)

Inform adults with UI and/or their carers Strong
regarding available treatment options
before deciding on containment alone.
Offer incontinence pads and/or containment Strong
devices for management of UI.
Lifestyle interventions
Examples of lifestyle factors that may be associated with UI

include obesity, smoking, level of physical activity and diet.
Modification of these factors may improve UI.

Encourage overweight and obese adults Strong
with UI to lose weight and maintain weight
loss.
Advise adults with UI that reducing caffeine Strong
intake may improve symptoms of urgency
and frequency but not incontinence.
Review type and amount of fluid intake in Weak
patients with UI.
Provide smoking cessation strategies to Strong
patients with UI who smoke.
Behavioural and physical therapies

Offer prompted voiding for adults with Strong
incontinence, who are cognitively impaired.
Offer bladder training as a first-line therapy Strong
to adults with UUI or MUI.
Offer supervised intensive pelvic floor Strong
muscle training (PFMT), lasting at least
three months, as a first-line therapy to
women with SUI or MUI (including the
elderly and post-natal).
Offer instruction on PFMT to men Strong
undergoing radical prostatectomy to
speed-up recovery from UI.
Ensure that PFMT programmes are as Strong
intensive as possible.

Do not offer electrical stimulation with Strong
surface electrodes (skin, vaginal, anal)
alone for the treatment of SUI.
Do not offer magnetic stimulation for the Strong
treatment of UI or overactive bladder in
women.
Consider percutaneous tibial nerve Strong
stimulation as an option for improvement
of UUI in women who have not benefited
from antimuscarinic medication.
Conservative therapy in MUI

Treat the most bothersome symptom first Weak
in patients with MUI.
Pharmacological Management
Antimuscarinics

Offer antimuscarinic drugs for adults with Strong
UUI who failed conservative treatment.
Consider extended release formulations of Strong
antimuscarinics drugs, whenever possible.
If an antimuscarinic treatment proves Strong
ineffective, consider dose escalation or
offering an alternative antimuscarinic
formulation, or mirabegron, or a
combination.

Encourage early review (of efficacy and Strong
side effects) of patients on antimuscarinic
medication for UUI.
Mirabegron

Offer antimuscarinic drugs or mirabegron Strong
to adults with UUI who failed conservative
treatment.
Antimuscarinic drugs in the elderly

Use long-term antimuscarinic treatment Strong
with caution in elderly patients especially
those who are at risk of, or have, cognitive
dysfunction.
Drugs for SUI

Offer Duloxetine in selected patients with Strong
symptoms of SUI when surgery is not
indicated.
Initiate and withdraw duloxetine using dose Strong
titration because of high risk of adverse
events.

Oestrogen

Offer long-term vaginal oestrogen therapy Strong
to post-menopausal women with UI and
symptoms of vulvo-vaginal atrophy.
In women with a history of breast Weak
cancer, the treating oncologist should be
consulted.
Discuss alternative hormone replacement Strong
therapies with women taking oral
conjugated equine oestrogen as hormone
replacement therapy who develop or
experience worsening UI.
Advise women who are taking systemic Strong
oestradiol who suffer from UI that stopping
the oestradiol is unlikely to improve their
UI.
Desmopressin

Consider offering desmopressin to patients Strong
requiring occasional short-term relief from
daytime UI and inform them that this drug
is not licensed for this indication.
Monitor plasma sodium levels in patients Strong
on desmopressin.
Do not use desmopressin for long-term Strong
control of UI.

Drug treatment in MUI

Offer antimuscarinic drugs or beta 3 Strong
agonists to patients with urgency-
predominant MUI.
Consider offering duloxetine to patients Strong
with MUI unresponsive to other
conservative treatments and who are not
seeking cure.
Surgical Management
The section considers surgical options for the following
situations:
• Women with uncomplicated SUI; this means no history
of previous surgery, no neurological lower urinary tract
dysfunction (LUTD), no bothersome genitourinary prolapse,
and those not considering further pregnancy.
• Women with complicated SUI. Neurogenic LUTD is
reviewed in the EAU Guidelines on Neuro-urology.
• Associated genitourinary prolapse has been included in
these Guidelines in terms of treating the incontinence, but
no attempt has been made to comment on treatment of
prolapse itself.
• Men with SUI, mainly those with post-prostatectomy
incontinence without neurological disease affecting the
lower urinary tract.
• Patients with refractory DO (detrusor overactivity)
incontinence.

Women with uncomplicated SUI

Offer a mid-urethral sling to women with Strong
uncomplicated SUI.
Inform women of the unique complications Strong
associated with each individual procedure.
Inform women who are being offered a Strong
single-incision sling that long-term efficacy
remains uncertain.
Inform women undergoing Strong
colposuspension that there is a longer
duration of surgery, hospital stay and
recovery, as well as a high risk of
development of pelvic organ prolapse and
voiding dysfunction post-operatively.
Inform older women with SUI about the Weak
increased risks associated with surgery,
including the lower probability of success.
Inform women that any vaginal surgery may Weak
have an impact on sexual function, which is
generally positive.
Only offer new devices, for which there Strong
is no level 1 evidence base, as part of a
structured research programme.
Only offer adjustable mid-urethral sling as Strong
a primary surgical treatment for SUI as part
of a structured research programme.
Offer bulking agents to women with SUI Strong
who request a low-risk procedure with
the understanding that repeat injections
are likely and long-term durability is not
established.

Women with complicated SUI

Management of complicated SUI should Weak
only be offered in expert centres*.
Base the choice of surgery for recurrent Weak
SUI on careful evaluation of the
individual patient including multichannel
urodynamics and imaging as appropriate.
Inform women with recurrent SUI that Weak
the outcome of a surgical procedure,
when used as a second-line treatment,
is generally inferior to its use as a
first-line treatment, both in terms of
reduced efficacy and increased risk of
complications.
Consider secondary synthetic sling, Weak
colposuspension or autologous sling as
first options for women with complicated
SUI.
Inform women receiving artificial urinary Weak
sphincter (AUS) or Adjustable Compression
device (ACT©) that although cure is
possible, even in expert centres, there is
a high risk of complications, mechanical
failure, or a need for explantation.
* Expert centres refers to the comments on surgeon volume in
the introduction to the surgical chapter.

Women with both stress urinary incontinence and
pelvic organ prolapse
Recommendations for women requiring Strength rating

surgery for bothersome pelvic organ
prolapse who have symptomatic or
unmasked SUI.
Offer simultaneous surgery for pelvic organ Strong
prolapse and SUI.
Inform women of the increased risk of Strong
adverse events with combined surgery
compared to prolapse surgery alone.
Recommendations for women requiring surgery for
bothersome pelvic organ prolapse without symptomatic
or unmasked SUI.
Inform women that there is a risk of Strong
developing de novo SUI after prolapse
surgery.
Warn women that the benefit of surgery for Strong
SUI may be outweighed by the increased
risk of adverse events with combined
surgery compared to prolapse surgery
alone.

Urethral diverticulum

Symptomatic urethral diverticula should be Strong
completely surgically removed.
Men with SUI

Offer duloxetine only to hasten recovery Weak
of continence after prostate surgery but
inform the patient about the possible
adverse events and that its use is off
label for this indication in most European
countries.
Only offer bulking agents to men with Weak
mild post-prostatectomy UI who desire
temporary relief of UI symptoms.
Do not offer bulking agents to men with Weak
severe post-prostatectomy UI.
Offer fixed slings to men with mild-to- Weak
moderate* post-prostatectomy UI.
Warn men that severe UI, prior pelvic Weak
radiotherapy or urethral stricture surgery,
may worsen the outcome of fixed male
sling surgery.
Offer artificial urinary sphincter (AUS) Weak
to men with moderate-to-severe post-
prostatectomy incontinence.
Implantation of AUS or ProACT© for men Weak
should only be offered in expert centres.

Warn men receiving AUS or ProACT© Weak
that, although cure can be achieved, even
in expert centres, there is a high risk of
complications, mechanical failure or a need
for explantation.
Do not offer non-circumferential Weak
compression device (ProACT®) to men who
have had pelvic radiotherapy.
*T he terms mild and moderate post-prostatectomy UI remain
undefined.
Surgical interventions for refractory detrusor

overactivity
Intravesical injection of botulinumtoxin A

Offer bladder wall injections of Strong
onabotulinum toxin A (100 U) to patients
with UUI refractory to conservative therapy
(such as pelvic floor muscle training and/or
drug treatment).
Warn patients of the limited duration of Strong
response, risk of urinary tract infection
and the possible prolonged need to self-
catheterise (ensure that they are willing
and able to do so).

Sacral nerve stimulation (neuromodulation)

Offer sacral nerve modulation to patients Strong
who have UUI refractory to antimuscarinic
therapy.
Cystoplasty/urinary diversion

Offer augmentation cystoplasty to patients Weak
with UI who have failed all other treatment
options.
Inform patients undergoing augmentation Weak
cystoplasty of the high risk of having
to perform clean intermittent self-
catheterisation (ensure they are willing and
able to do so) and that they need lifelong
surveillance.
Do not offer detrusor myectomy as a Weak
treatment for UI.
Only offer urinary diversion to patients Weak
who have failed less invasive therapies for
the treatment of UI and who will accept a
stoma and have been warned about the
possible small risk of malignancy.

Surgery in patients with MUI

Warn patients with MUI that surgery is less Strong
likely to be successful than surgery for SUI
alone.
Inform women with MUI that one single Strong
treatment may not cure UI; it may be
necessary to treat other components of the
incontinence problem as well as the most
bothersome symptom.
Surgery for UI in the elderly

Inform older women with UI about the Weak
increased risks associated with surgery
(including onabotulinum toxin A injection),
together with the lower probability of
benefit.

Figure 1: Women presenting with urinary incontinence

Figure 2: Men presenting with urinary incontinence

Non Obstetric Urinary Fistula*

General
Surgeons undertaking complex pelvic Weak
surgery should be competent at identifying,
preserving and repairing the ureter.
Do not routinely use ureteric stents as Weak
prophylaxis against injury during routine
gynaecological surgery.
Suspect ureteric injury or fistula in patients Weak
following pelvic surgery if a fluid leak
or pelvicalyceal dilatation occurs post-
operatively or if drainage fluid contains high
levels of creatinine.
Suspect uretero-arterial fistula in patients Weak
presenting with haematuria with a history
of relevant surgery.
Use three dimensional imaging techniques Weak
to diagnose and localise urinary fistulae.
Manage upper urinary tract fistulae by Weak
conservative or endoluminal technique
where such expertise and facilities exists.
Surgical principles
Surgeons involved in fistula surgery Weak
should have appropriate training, skills,
and experience to select an appropriate
procedure for each patient.
Attention should be given as appropriate Weak
to skin care, nutrition, rehabilitation,
counselling and support prior to, and
following, fistula repair.

If a vesicovaginal fistula is diagnosed within Weak
six weeks of surgery, consider indwelling
catheterisation for a period of up to twelve
weeks after the causative event.
Tailor the timing of fistula repair to Weak
the individual patient and surgeon
requirements once any oedema,
inflammation, tissue necrosis, or infection,
are resolved.
Where concurrent ureteric re-implantation Weak
or augmentation cystoplasty are required,
the abdominal approach is necessary.
Ensure that the bladder is continuously Weak
drained following fistula repair until healing
is confirmed (expert opinion suggests:
10-14 days for simple and/or post-surgical
fistulae; 14-21 days for complex and/or post-
radiation fistulae).
Where urinary and/or faecal diversions are Weak
required, avoid using irradiated tissue for
repair.
Use interposition grafts when repair of Weak
radiation associated fistulae is undertaken.
In patients with intractable UI from Weak
radiation-associated fistula, where
life expectancy is very short, consider
performing ureteric occlusion.
Repair persistent ureterovaginal fistula Weak
by an abdominal approach using open,
laparoscopic or robotic techniques
according to availability and competence.

Consider palliation by nephrostomy tube Weak
diversion and endoluminal distal ureteric
occlusion for patients with ureteric fistula
associated with advanced pelvic cancer
and poor performance status.
Urethrovaginal fistulae should preferably be Weak
repaired by a vaginal approach.
*T hese recommendations are derived from the ICUD 2013
review and have not been fully validated by the EAU
Guidelines Office methodology.

the European Association of Urology at their website,

EAU GUIDELINES ON NEURO-UROLOGY
B. Blok (Chair), J. Pannek (Vice-chair) D. Castro-Diaz,

G. Del Popolo, J. Groen, R. Hamid, G. Karsenty, T.M. Kessler
Guidelines Associates: H. Ecclestone, S. Musco,
B. Padilla-Fernández, V. Phé, A. Sartori, L. ‘t Hoen
Introduction
Neuro-urological disorders can cause a variety of long-term
complications; the most dangerous being damage of renal
function. Treatment and intensity of follow-up examinations
are based on the type of neuro-urological disorder and the
underlying cause.
Terminology
The terminology used and the diagnostic procedures outlined
in this document follow those published by the International
Continence Society (ICS).
Risk factors and epidemiology

All central and peripheral neurological disorders carry a high
risk of causing functional disturbances of the urinary tract.
Classification
The pattern of lower urinary tract (LUT) dysfunction following
neurological disease is determined by the site and nature of
the lesion. A very simple classification system, for use in daily
clinical practice, to decide on the appropriate therapeutic
approach is provided in Figure 1.
Neuro-Urology 179
Figure 1: Patterns of lower urinary tract dysfunction following
neurological disease
A Suprapontine lesion Over-

• History: predominantly storage symptoms active
• Ultrasound: insigniﬁcant PVR urine volume
• Urodynamics: detrusor overactivity
Normo-active
B
Spinal (infrapontine–suprasacral) lesion Over-

• History: both storage and voiding symptoms active
• Ultrasound: PVR urine volume usually raised
• Urodynamics: detrusor overactivity, detrusor–sphincter
dyssynergia Overactive
C
Sacral/infrasacral lesion Under- Under-
• History: predominantly voiding symptoms active active
• Ultrasound: PVR urine volume raised
• Urodynamics: hypocontractile or
acontractile detrusor Normo-active Underactive
The pattern of LUT dysfunction following neurological disease

is determined by the site and nature of the lesion. Panel A
denotes the region above the pons, panel B the region
between the pons and sacral cord and panel C the sacral cord
and infrasacral region. Figures on the right show the expected
dysfunctional states of the detrusor-sphincter system. Figure
adapted from Panicker et al. with permission from Elsevier.
PVR = post-void residual.
Early diagnosis and treatment are essential in both congenital
and acquired neuro-urological disorders, even in the presence
180 Neuro-Urology
of normal neurological reflexes. Neuro-urological disorders
can be the presenting feature of neurological pathology and
early intervention can prevent irreversible deterioration of the
lower and upper urinary tract.
Patient assessment
Diagnosis of neuro-urological disorders should be based
on a comprehensive assessment of neurological and
non-neurological conditions. Initial assessment should include
a detailed history, physical examination, and urinalysis.
History
An extensive general and specific history is mandatory and
should concentrate on past and present symptoms, disorders
of the urinary tract as well as bowel, sexual and neurological
function. Special attention should be paid to possible warning
signs and symptoms (e.g. pain, infection, haematuria, fever)
that warrant further investigation.
The neurological status should be described as completely
as possible. All sensations and reflexes in the urogenital area
must be tested, including detailed testing of the anal sphinc-
ter and pelvic floor functions (Figure 2). Availability of this
clinical information is essential for the reliable interpretation
of subsequent diagnostic investigations.
Neuro-Urology 181
Figure 2: Lumbosacral dermatomes, cutaneous nerves, and
reflexes
A B
T12 Genitofemoral and
Subcostal nerve Iliohypogastric nerve
(T12) Pudendal nerve
L1
Iliohypogastric
nerve (L1) L3
L2
Dorsal rami
(L1, L2, L3)
S2
S3 S4 Obturator nerve
S5 S4
Dorsal rami
S3 S5
(S1, S2, S3)
Lateral
cutaneous
nerve of
thigh (L2, L3)
L2 Gluteal branches of
Obturator nerve posterior cutaneous
(L2, L3, L4) nerve of thigh
Posterior
S2
L3 cutaneous nerve
of thigh
(S1, S2, S3)
C D
Ilioinguinal nerve Dorsal nerve of penis L1
Cremasteric reflex
L2
T12 Knee reflex L3
L4
L5
L1
S1
Ankle reflex
S3 S2
S4 Genitofemoral
nerve S3 Bulbocavernosus reflex
Anal reflex
S4
S5
L2
Pudendal nerve
The physical examination includes testing sensations and

reflexes mediated through the lower spinal cord. Abnormal
findings would suggest a lesion affecting the lumbosacral
segments; mapping out distinct areas of sensory impairment
helps to further localise the site of lesion. Distribution of
dermatomes (areas of skin mainly supplied by a single spinal
nerve) and cutaneous nerves over the perianal region and
back of the upper thigh (A), the perineum (B), male external
genitalia (C) and root values of lower spinal cord reflexes (D).
Figure adapted from Panicker et al., with parts A-C adapted
from Standring, both with permission from Elsevier.
182 Neuro-Urology
Recommendations for history taking and physical
examination

History taking
Take an extensive general history, concen- Strong
trating on past and present symptoms.
Take a specific history for each of the four Strong
mentioned functions - urinary, bowel,
sexual and neurological.
Pay special attention to the possible Strong
existence of alarm signs (e.g. pain,
infection, haematuria, fever) that warrant
further specific diagnosis.
Assess quality of life when evaluating and Strong
treating the neuro-urological patient.
Use available validated tools including the Strong
Qualiveen and I-QoL for urinary symptoms
and the QoL-BM for bowel dysfunction in
multiple sclerosis and spinal cord injury
patients. In addition, generic (SF-36 or
KHQ) questionnaires can be used.
Use MSISQ-15 and MSISQ-19 to Strong
evaluate sexual function in multiple
sclerosis patients.
Acknowledge individual patient disabilities Strong
when planning further investigations.
Describe the neurological status as com- Strong
pletely as possible, sensations and reflexes
in the urogenital area must all be tested.
Test the anal sphincter and pelvic floor Strong
functions.
Neuro-Urology 183
Perform urinalysis, blood chemistry, Strong
bladder diary, residual and free flowmetry,
incontinence quantification and urinary
tract imaging.
I-QoL = Incontinence Quality of Life Instrument; OoL-BM =
Quality of Life Bowel Management scoring tool; KHQ = King’s
Health Questionnaire; SF-36 = Short Form 36-item Health
Survey Questionnaires; MSISQ 15/19 = Multiple Sclerosis
Intimacy and Sexuality Questionnaire 15/19 question version.
Urodynamic tests
Bladder diaries are considered a valuable diagnostic tool
in patients with neuro-urological disorders. A bladder
diary should be recorded for at least two to three days.
Uroflowmetry and ultrasound assessment of post-void
residual should be repeated at least two or three times in
patients able to void. Invasive urodynamic studies comprise
mandatory assessment tools to determine the exact type of
neuro-urological disorder. Video-urodynamics combines
filling cystometry and pressure flow studies with radiological
imaging. Currently, video-urodynamics is considered to
provide the most comprehensive information for evaluating
neuro-urological disorders.
Recommendations for urodynamics and

uro-neurophysiology

Perform a urodynamic investigation to Strong
detect and specify lower urinary tract
(dys-)function, use same session repeat
measurement as it is crucial in clinical
decision making.
184 Neuro-Urology
Non-invasive testing is mandatory before Strong
invasive urodynamics is planned.
Use video-urodynamics for invasive Strong
urodynamics in neuro-urological patients.
If this is not available, then perform a filling
cystometry continuing into a pressure flow
study.
Use a physiological filling rate and body- Strong
warm saline.
Treatment
The primary aims and their prioritisation when treating neuro-
urological disorders are:
1. protection of the upper urinary tract;
2. improvement of urinary continence;
3. restoration of (parts of) LUT function;
4. improvement of the patient’s QoL.
Further considerations are the patient’s disability, cost-effec-

tiveness, technical complexity, and possible complications.
Conservative treatment
Assisted bladder emptying
Triggered reflex voiding is not recommended as there is a risk
of pathologically elevated bladder pressures. Only in the case
of absence, or surgically reduced outlet obstruction it may be
an option.
Caution: bladder compression techniques to expel urine

(Credé) and voiding by abdominal straining (Valsalva
manoeuvre) create high pressures and are potentially
hazardous, and their use should be discouraged.
Neuro-Urology 185
Rehabilitation
In selected patients, pelvic floor muscle exercises, pelvic floor
electro-stimulation, and biofeedback might be beneficial.
External appliances
Social continence for the incontinent patient can be achieved
using an appropriate method of urine collection.
Medical therapy
A single, optimal, medical therapy for patients with neuro-
urological symptoms is not yet available. Muscarinic
receptor antagonists are the first-line choice for treating
neuro-urological disorders.
Recommendations on drug treatment

Use antimuscarinic therapy as the first-line Strong
medical treatment for neurogenic detrusor
overactivity.
Offer intravesical oxybutynin to neurogenic Strong
detrusor overactivity patients with poor
tolerance to the oral route.
Prescribe α-blockers to decrease bladder Strong
outlet resistance.
Do not prescribe parasympathomimetics Strong
for underactive detrusor.
186 Neuro-Urology
Recommendations for catheterisation

Use intermittent catheterisation, whenever Strong
possible aseptic technique, as a standard
treatment for patients who are unable to
empty their bladder.
Thoroughly instruct patients in the Strong
technique and risks of intermittent
catheterisation.
Avoid indwelling transurethral and supra- Strong
pubic catheterisation whenever possible.
Recommendations for minimal invasive treatment

Use botulinum toxin injection in the Strong
detrusor to reduce neurogenic detrusor
overactivity in multiple sclerosis or spinal
cord injury patients if antimuscarinic
therapy is ineffective.
Bladder neck incision is effective in a Strong
fibrotic bladder neck.
Neuro-Urology 187
Recommendations for surgical treatment

Perform bladder augmentation in order Strong
to treat refractory neurogenic detrusor
overactivity.
Place an autologous urethral sling in Strong
female patients with neurogenic stress
urinary incontinence who are able to self-
catheterise.
Insert an artificial urinary sphincter in male Strong
patients with neurogenic stress urinary
incontinence.
Urinary tract infections (UTI)

Patients with neuro-urological disorders, especially those with
spinal cord injury, may have other signs and symptoms in
addition to, or instead of, traditional signs and symptoms of a
UTI in able-bodied individuals.
Recommendations for the treatment of UTI

Do not screen for or treat asymptomatic Strong
bacteriuria in patients with neuro-
urological disorders.
Avoid the use of long-term antibiotics for Strong
recurrent urinary tract infections (UTIs).
In patients with recurrent UTI, optimise Strong
treatment of neuro-urological symptoms
and remove foreign bodies (e.g. stones,
indwelling catheters) from the urinary tract.
188 Neuro-Urology
Individualise UTI prophylaxis in patients Strong
with neuro-urological disorders as there is
no optimal prophylactic measure available.
Sexual (dys)function and fertility

Patients with neurological disease often suffer from sexual
dysfunction, which frequently impairs QoL.
Recommendations for erectile dysfunction and male

fertility

Prescribe oral phosphodiesterase type 5 Strong
inhibitors as first-line medical treatment in
neurogenic erectile dysfunction.
Give intracavernous injections of Strong
vasoactive drugs (alone or in combination)
as second-line medical treatment in
Offer mechanical devices such as vacuum Strong
devices and rings to patients with
Perform vibrostimulation and transrectal Strong
electroejaculation for sperm retrieval in
men with spinal cord injury.
Perform microsurgical epididymal sperm Strong
aspiration, testicular sperm extraction and
intracytoplasmic sperm injection after
failed vibrostimulation and/or transrectal
electroejaculation in men with spinal cord
injury.
Neuro-Urology 189
Counsel men with spinal cord injury at or Strong
above Th 6 and fertility clinics about the
potentially life-threatening condition of
autonomic dysreflexia.
Recommendations on female sexuality and fertility

Do not offer medical therapy for the Strong
treatment of neurogenic sexual dysfunction
in women.
Take a multidisciplinary approach, Strong
tailored to individual patient’s needs and
preferences, in the management of fertility,
pregnancy and delivery in women with
neurological diseases.
Follow-up
Neuro-urological disorders are often unstable and the
symptoms may vary considerably, even within a relatively
short period. Regular follow-up is therefore necessary.
Recommendations for follow-up

Assess the upper urinary tract at regular Strong
intervals in high risk patients.
Perform a physical examination and urine Strong
laboratory every year in high risk patients.
Any significant clinical changes should Strong
instigate further, specialised, investigation.
Perform urodynamic investigation as a Strong
mandatory baseline diagnostic intervention
in high-risk patients at regular intervals.
190 Neuro-Urology
Summary
Neuro-urological disorders present a multifaceted pathology.
Extensive investigation and a precise diagnosis are required
before the clinician can initiate individualised therapy.
Treatment must take into account the patient’s medical and
physical condition and expectations with regard to his/her
future social, physical, and medical situation.

Neuro-Urology 191
EAU GUIDELINES ON MALE SEXUAL
DYSFUNCTION: Erectile Dysfunction
and Premature Ejaculation
K. Hatzimouratidis (Chair), F. Giuliano, I. Moncada, A. Muneer,

A. Salonia (Vice-chair), P. Verze
Guideline Associates: A. Parnham, E.C. Serefoglu
ERECTILE DYSFUNCTION
Introduction
Erectile dysfunction (ED) is defined as the persistent inability
to attain and maintain an erection sufficient to permit
satisfactory sexual performance. Erectile dysfunction may
affect physical and psychosocial health and may have a
significant impact on the quality of life (QoL) of sufferers and
their partners. There is increasing evidence that ED can also
be an early manifestation of coronary artery and peripheral
vascular disease; therefore, ED should not be regarded only
as a QoL issue, but also as a potential warning sign of
cardiovascular disease (CVD).
192 Male Sexual Dysfunction

Table 1: Pathophysiology of erectile dysfunction
Vasculogenic
Recreational habits (e.g. cigarette smoking)
Lack of regular physical exercise
Obesity
Cardiovascular diseases (e.g. hypertension, coronary artery
disease; peripheral vasculopathy, etc.)
Type 1 and 2 diabetes mellitus; hyperlipidaemia; metabolic
syndrome; hyperhomocysteinemia, etc.
Major pelvic surgery (radical prostatectomy) or radiotherapy
(pelvis or retroperitoneum)
Neurogenic
Central causes
Degenerative disorders (e.g., multiple sclerosis, Parkinson’s
disease, multiple atrophy, etc.)
Spinal cord trauma or diseases
Stroke
Central nervous system tumours
Peripheral causes
Type 1 and 2 diabetes mellitus
Chronic renal failure; chronic liver failure
Polyneuropathy
Surgery (major surgery of pelvis/retroperitoneum) or
radiotherapy (pelvis or retroperitoneum)
Surgery of the urethra (urethral stricture, urethroplasty, etc.)
Anatomical or structural
Hypospadias; epispadias; micropenis
Phimosis
Peyronie’s disease
Penile cancer (other tumors of the external genitalia)
Male Sexual Dysfunction 193

Hormonal
Diabetes Mellitus; Metabolic Syndrome;
Hypogonadism (any type)
Hyperprolactinaemia
Hyper- and hypothyroidism
Hyper- and hypocortisolism (Cushing’s disease, etc.)
Panhypopituitarism and multiple endocrine disorders
Mixed pathophysiology pathways
Chronic systemic diseases (e.g., diabetes mellitus;
hypertension; metabolic syndrome; chronic renal failure;
chronic liver disorders; hyperhomocysteinemia; obstructive
sleep apnoea; etc.)
Psoriasis; gouty arthritis; ankylosing spondylitis;
non-alcoholic fatty liver; chronic periodontitis; open-angle
glaucoma; inflammatory bowel disease
Iatrogenic causes (e.g. transrectal ultrasonography-guided
prostate biopsy, etc.)
Drug-induced
Antihypertensives (e.g., thiazide diuretics, beta-blockers, etc.)
Antidepressants (selective serotonin re-uptake inhibitors,
tricyclics)
Antipsychotics (e.g., neuroleptics, etc.)
Antiandrogens (GnRH analogues and antagonists; 5-ARIs)
Recreational drugs (e.g., alcohol, heroin, cocaine, marijuana,
methadone, synthetic drugs, anabolic steroids, etc.)
Psychogenic
Generalised type (e.g., lack of arousability and disorders of
sexual intimacy)
Situational type (e.g., partner-related, performance-related
issues or due to distress)

Trauma
Penile fracture
Pelvic fractures
GnRH = Gonadotropin-releasing hormone;
5-ARIs = 5α-Reductase inhibitors
Figure 1: Minimal diagnostic evaluation (basic work-up) in

patients with erectile dysfunction
Paent with ED (self-reported)
Medical and psychosexual history (use of validated instruments, e.g. IIEF)
Idenfy other than Idenfy common Idenfy reversible Assess psychosocial

ED sexual problems causes of ED risk factors for ED status
Focused physical examinaon
Signs of Cardiovascular and

Penile deformies Prostac disease
hypogonadism neurological status
Laboratory tests
Total testosterone (morning sample)

Glucose-lipid profile
if indicated, bio-available or free
(if not assessed in the last 12 months)
testosterone
ED = erectile dysfunction; IIEF = International Index of Erectile

Function.
Table 2: Cardiac risk stratification (based on 2nd Princeton
Consensus)
Low-risk category Intermediate-risk High-risk category

category
Asymptomatic, ≥ 3 risk factors for High-risk
< 3 risk factors for CAD (excluding arrhythmias
CAD (excluding sex)
sex)
Mild, stable angina Moderate, stable Unstable or
(evaluated and/or angina refractory angina
being treated)
Uncomplicated Recent MI Recent MI
previous MI (> 2, < 6 weeks) (< 2 weeks)
LVD/CHF LVD/CHF LVD/CHF
(NYHA class I or II) (NYHA class III) (NYHA class IV)
Post-successful Non-cardiac Hypertrophic
coronary sequelae of obstructive
revascularisation atherosclerotic and other
disease (e.g., cardiomyopathies
stroke, peripheral
vascular disease)
Controlled Uncontrolled
hypertension hypertension
Mild valvular Moderate-to-
disease severe valvular
disease
CAD = coronary artery disease; CHF = congestive heart failure;
LVD = left ventricular dysfunction; MI = myocardial infarction;
NYHA = New York Heart Association.

Table 3: Indications for specific diagnostic tests
Primary ED (not caused by organic disease or psychogenic

disorder).
Young patients with a history of pelvic or perineal trauma,
who could benefit from potentially curative revascularisation
surgery or angioplasty.
Patients with penile deformities which might require surgical
correction (e.g., Peyronie’s disease, congenital penile
curvature).
Patients with complex psychiatric or psychosexual disorders.
Patients with complex endocrine disorders.
Specific tests may be indicated at the request of the patient
or his partner.
Medico-legal reasons (e.g., implantation of penile prosthesis
to document end stage ED, sexual abuse).
Table 4: Specific diagnostic tests
Nocturnal Penile Tumescence and Rigidity using Rigiscan®.

Vascular studies:
- Intracavernous vasoactive drug injection.
- Penile Dynamic Duplex Ultrasonography.
- Penile Dynamic Infusion Cavernosometry and
Cavernosography.
- Internal pudendal arteriography.
Neurological studies (e.g., bulbocavernosus reflex latency,
nerve conduction studies).
Endocrinological studies.
Specialised psychodiagnostic evaluation.

Recommendations for the diagnosis of Strength rating
erectile dysfunction
Take a comprehensive medical and sexual Strong
history in every patient.
Use a validated questionnaire related to Strong
erectile dysfunction to assess all sexual
function domains and the effect of a
specific treatment modality.
Include a physical examination in the initial Strong
assessment of men with erectile dysfunc-
tion (ED) to identify underlying medical
conditions and comorbid genital disorders
that may be associated with ED.
Assess routine laboratory tests, including Strong
glucose-lipid profile and total testosterone,
to identify and treat any reversible risk
factors and lifestyle factors that can be
modified.
Include specific diagnostic tests in the Strong
initial evaluation only in the presence of the
conditions presented in Table 3.

Disease management
Figure 2: Management algorithm for erectile dysfunction

Management of erecle dysfuncon
Idenfy and treat Lifestyle changes and Provide educaon

“curable” causes of risk factor and counselling to
erecle dysfuncon modificaons paent (and partner,
as appropriate)
Idenfy paent needs and expectaons

Shared decision-making
Offer conjoint psycho-sexual and
medical/physical treatment
Phosphodiesterase type 5 inhibitor

Topical/intraurethral alprostadil
Vacuum device
Low intensity shockwave treatment
Assess therapeuc outcomes

• Paent self-perceived treatment invasiveness
• Treatment-associated improvement in
Inadequate treatment outcome
erecle funcon
• Treatment-related side effects
• Treatment-associated sasfacon
• Assess adequate use of treatment opons

• Provide new instrucons and counselling
• Re-trial
• Consider treatment alternave or
combined therapies

• Paent self-perceived treatment invasiveness
• Treatment-associated improvement in
erecle funcon
Intracavernosal injecons
Penile prostheses


Table 5: Summary of the key pharmacokinetic data for the
four PDE5 inhibitors currently EMA-approved to
treat erectile dysfunction*
Parameter Sildenafil, Tadalafil, Vardenafil, Avanafil

100 mg 20 mg 20 mg 200mg
Cmax 560 μg/L 378 μg/L 18.7 μg/L 5.2 μg/L
Tmax (median) 0.8-1 2 hours 0.9 hours 0.5-0.75
hours hours
T1/2 2.6-3.7 17.5 3.9 hours 6-17 hours
hours hours
AUC 1,685 8,066 56.8 μg.h/L 11.6 μg.h/L
μg.h/L μg.h/L
Protein 96% 94% 94% 99%
binding
Bioavailability 41% NA 15% 8-10%
* Fasted state, higher recommended dose. Data adapted from
EMA statements on product characteristics.
Cmax: maximal concentration, Tmax: time-to-maximum plasma
concentration; T1/2: plasma elimination half-time; AUC: area
under curve or serum concentration time curve.

Table 6: Common adverse events of the four PDE5 inhibitors
currently EMA-approved to treat erectile
dysfunction*
Adverse Sildenafil Tadalafil Vardenafil Avanafil

event 200mg
Headache 12.8% 14.5% 16% 9.3%
Flushing 10.4% 4.1% 12% 3.7%
Dyspepsia 4.6% 12.3% 4% uncommon
Nasal 1.1% 4.3% 10% 1.9%
congestion
Dizziness 1.2% 2.3% 2% 0.6%
Abnormal 1.9% < 2% none
vision
Back pain 6.5% < 2%
Myalgia 5.7% < 2%
* Adapted from EMA statements on product characteristics.

Table 7: Penile prostheses models available on the market
Semi-rigid Inflatable
prostheses prostheses
Two-piece Three piece
Spectra ™ Ambicor™ [AMS] Titan OTR ™ (One Touch
[AMS] Release) [Coloplast]
Genesis ™ Titan OTR NB ™
[Mentor] (Narrow base) [Coloplast]
Titan Zero Degree ™
Tube ™ AMS 700 CX ™
[Promedon] [Boston Scientific]
ZSI 100 ™ AMS 700 LGX ™
[Zephyr] [Boston Scientific]
Virilis II ™ AMS 700 CXR ™
[Subrini] [Boston Scientific]
ZSI 475 ™ [Zephyr]

erectile dysfunction
Enact lifestyle changes and risk factor Strong
modification prior to or accompanying
erectile dysfunction (ED) treatment.
Support the resumption of sexual activity Strong
through pro-erectile treatments at the
earliest opportunity after radical
prostatectomy.
Treat a curable cause of ED first, when Weak
found.
Use phosphodiesterase type 5 inhibitors Strong
(PDE5Is) as first-line therapy.

Assess all patients for inadequate/incorrect Weak
information about the mechanism of action
and the ways in which drugs should be
taken, since they are the main causes of a
lack of response to PDE5Is.
Use vacuum erection devices as a first-line Weak
therapy in well-informed older patients
with infrequent sexual intercourse and
comorbidity requiring non-invasive, drug-
free management of ED.
Use low intensity shockwave therapy in Weak
mild organic ED patients or poor
responders to PDE5Is.
Use topical/intraurethral Alprostadil as an Weak
alternative to intracavernous injections in
patients who prefer a less-invasive therapy.
Use intracavernous injections as second- Strong
line therapy.
Use implantation of a penile prosthesis as Strong
third-line therapy.
PREMATURE EJACULATION (PE)

Introduction
Although PE is a common male sexual dysfunction, it is poorly
understood. Patients are often unwilling to discuss their
symptoms and many physicians do not know about effective
treatments. As a result, patients may be misdiagnosed or
mistreated.
PE (lifelong and acquired) is a male sexual dysfunction

characterised by the following:
1. Ejaculation that always or nearly always occurs prior to or
within about 1 minute of vaginal penetration (lifelong PE) or

a clinically significant and bothersome reduction in latency
time, often to about 3 minutes or less (acquired PE);
2. The inability to delay ejaculation on all or nearly all vaginal
penetrations;
3. Negative personal consequences, such as distress, bother,
frustration and/or the avoidance of sexual intimacy.

evaluation of premature ejaculation
Perform the diagnosis and classification Strong
of premature ejaculation (PE) based on
medical and sexual history, which should
include assessment of intravaginal
ejaculatory latency time (IELT)
(self-estimated), perceived control, distress
and interpersonal difficulty due to the
ejaculatory dysfunction.
Do not use stopwatch-measured IELT in Weak
clinical practice.
Use patient-reported outcomes in daily Weak
clinical practice.
Include physical examination in the initial Strong
assessment of PE to identify anatomical,
abnormalities that may be associated
with PE or other sexual dysfunctions,
particularly erectile dysfunction.
Do not perform routine laboratory or Strong
neurophysiological tests. They should only
be directed by specific findings from history
or physical examination.

Disease management

premature ejaculation
Treat ED, other sexual dysfunction or Strong
genitourinary infection (e.g. prostatitis)
first.
Use pharmacotherapy as first-line treat- Strong
ment of lifelong premature ejaculation (PE).
Use off-label topical anaesthetic agents as Strong
a viable alternative to oral treatment with
selective serotonin re-uptake inhibitors
(SSRIs).
Use tramadol on demand as a weak Strong
alternative to SSRIs.
Use PDE5Is alone or in combination with Strong
other therapies in patients with PE (without
ED).
Use psychological/behavioural therapies Weak
in combination with pharmacological treat-
ment in the management of acquired PE.

Figure 3: Management of premature ejaculation*
Clinical diagnosis of premature ejaculaon

based on paent +/- partner history
• Time to ejaculaon (IELT)
• Perceived degree of ejaculatory control
• Degree of bother/stress
• Onset and duraon of PE
• Psychosocial/relaonship issues
• Medical history
• Physical examinaon
Treatment of premature ejaculaon

Paent counselling/educaon
Discussion of treatment opons
If PE is secondary to ED, treat ED first or
concomitantly
• Pharmacotherapy (recommended as first-line

treatment opon in lifelong PE)
o Dapoxene for on-demand use (the only
approved drug for PE)
o Off-label treatments include chronic daily use
of andepressants (SSRIs or clomipramine)
and topical anaesthecs or oral tramadol on
demand
• Behavioural therapy, includes stop/start
technique, squeeze and sensate focus
• Combinaon treatment
* Adapted from Lue et al. 2004.

ED = erectile dysfunction; PE = premature ejaculation;
IELT = intravaginal ejaculatory latency time; SSRI = selective
serotonin receptor inhibitor.


EAU GUIDELINES ON
PRIAPISM

Introduction
Priapism is a pathological condition representing a true
disorder of penile erection that persists for more than four
hours and is beyond or unrelated to sexual interest or
stimulation. Erections lasting up to four hours are defined by
consensus as ‘prolonged’. Priapism may occur at all ages.
Classification
Ischaemic priapism is a persistent erection marked by rigidity
of the corpora cavernosa and by little or no cavernous arterial
inflow, although often proximally there is a compensated high
velocity picture with little blood flow distally. The patient
typically complains of penile pain and clinical examination
reveals a rigid erection.
Non-ischaemic priapism is a persistent erection caused by

unregulated cavernous arterial inflow. The patient typically
reports an erection that is not fully rigid and is not associated
with pain although fully rigid erections may still occur with
sexual stimulation.
Stuttering (recurrent or intermittent) priapism is a distinct

condition that is characterised by repetitive and painful
episodes of prolonged erections. Erections are often
208 Priapism
self-limited with intervening periods of detumescence. These
are analogous to repeated episodes of ischaemic (or low flow)
priapism. The duration of the erectile episodes is generally
shorter than in ischaemic priapism. The frequency and/or
duration of these episodes is variable and a single episode
can sometimes progress into a full-blown ischaemic priapism.
Ischaemic (Low-Flow or Veno-Occlusive) Priapism
Table 1: Key points when taking the history of priapism
Duration of erection
Presence and severity of pain
Previous episodes of priapism and method of treatment
Current erectile function, especially the use of any
erectogenic therapies prescription or nutritional
supplements
Medications and recreational drug use
Sickle cell disease, haemoglobinopathies, hypercoagulable
states
Trauma to the pelvis, perineum, or penis
Priapism 209
Table 2: Key findings in priapism
Ischaemic Non-
priapism ischaemic
priapism
Corpora cavernosa fully rigid Usually Seldom
Penile pain Usually Seldom
Abnormal penile blood gas Usually Seldom
Haematological abnormalities Sometimes Seldom
Recent intracavernosal Sometimes Sometimes
injection
Perineal trauma Seldom Usually
Table 3: Typical blood gas values
Source pO2 pCO2 pH

(mmHg) (mmHg)
Normal arterial blood > 90 < 40 7.40
(room air)
[similar values are found
in arterial priapism]
Normal mixed venous 40 50 7.35
blood (room air)
Ischaemic priapism (first < 30 > 60 < 7.25
corporal aspirate)
210 Priapism
ischaemic priapism
Take a comprehensive history to establish Strong
the diagnosis which can help to determine
the priapism subtype.
Include a physical examination of the Strong
genitalia, the perineum and the abdomen
in the diagnostic evaluation.
For laboratory testing, include complete Strong
blood count, white blood count with blood
cell differential, platelet count and
coagulation profile. Direct further
laboratory testing based on history, clinical
and laboratory findings. In children with
priapism, perform a complete evaluation
of all possible causes.
Analyse the blood gas parameters from Strong
blood aspirated from the penis to
differentiate between ischaemic and
non-ischaemic priapism.
Perform colour duplex ultrasound of the Strong
penis and perineum for the differentiation
between ischaemic and non-ischaemic
priapism as an alternative or adjunct to
blood gas analysis.
In cases of prolonged ischaemic priapism, Strong
use magnetic resonance imaging of the
penis to predict smooth muscle viability
and confirm erectile function restoration.
Perform selected pudendal arteriogram Strong
when embolisation is planned for the
management of non-ischaemic priapism.
Priapism 211
Disease Management
The treatment is sequential and the physician should move on
to the next stage if the treatment fails.
Figure 1: Treatment of ischaemic priapism
Inial conservave measures

• Local anaesthesia of the penis
• Insert wide bore buerfly (16-18 G) through the glans into the corpora cavernosa
• Aspirate cavernosal blood unl bright red arterial blood is obtained
Cavernosal irrigaon
• Irrigate with 0.90% w/v saline soluon
Intracavernosal therapy
• Inject intracavernosal adrenoceptor agonist
• Current first-line therapy is phenylephrine* with aliquots of 200 µg being injected every 3-5
minutes unl detumescence is achieved (Maximum dose of phenylephrine is 1mg within 1 hour)*
Surgical therapy
• Surgical shunng
• Consider primary penile implantaon if priapism has been present for more than 36 hours
* The dose of phenylephrine should be reduced in children.

It can result in significant hypertension and should be used
with caution in men with cardiovascular disease.
Monitoring of pulse, blood pressure and electrocardiogram
(ECG) is advisable in all patients during administration and
for 60 minutes afterwards. Its use is contraindicated in men
with a history of cerebro-vascular disease and significant
hypertension.
212 Priapism
Table 4: Medical treatment of ischaemic priapism
Drug Dosage/Instructions for use

Phenylephrine • Intracavernous injection of 200 μg
every three to five minutes.
• Maximum dosage is 1 mg within one
hour.
• Lower doses are recommended in
children and patients with severe
cardiovascular disease.
Etilephrine • Intracavernosal injection at a
concentration of 2.5 mg in 1-2 mL
normal saline.
Methylene blue • Intracavernous injection of
50-100 mg, left for five minutes.
It is then aspirated and the penis
compressed for an additional five
minutes.
Adrenaline • Intracavernous injection of 2 mL of
1/100,000 adrenaline solution up
to five times over a twenty minute
period.
Terbutaline • Oral administration of 5 mg for
prolonged erections lasting more
than 2.5 hours, after intracavernous
injection of vasoactive agents.

ischaemic priapism
Start management of ischaemic priapism Strong
as early as possible (within four to six
hours) and follow a stepwise approach.
Priapism 213
First, decompress the corpora cavernosa Weak
by penile aspiration until fresh red blood is
obtained.
In priapism secondary to intracavernous Strong
injections of vasoactive agents, replace blood
aspiration with intracavernous injection of
a sympathomimetic drug as the first step.
In priapism that persists despite aspiration, Strong
proceed to the next step, which is intra-
cavernous injection of a sympathomimetic
drug.
In cases that persist despite aspiration and Strong
intracavernous injection of a sympathomi-
metic drug, repeat these steps several times
before considering surgical intervention.
Treat ischaemic priapism due to sickle cell Strong
anaemia in the same fashion as idiopathic
ischaemic priapism. Provide other
supportive measures (intravenous
hydration, oxygen administration with
alkalisation with bicarbonates, blood
exchange transfusions), but do not delay
initial treatment to the penis.
Proceed to surgical treatment only when Strong
blood aspiration and intracavernous
injection of sympathomimetic drugs have
failed or for priapism events lasting < 72 hours.
Perform distal shunt surgical procedures Strong
first followed by proximal procedures in
case of failure.
Consider insertion of a penile prosthesis if Strong
priapism episode is > 36 hours after onset,
or in cases for which all other interventions
have failed.
214 Priapism
Non-ischaemic (High-Flow or Arterial) Priapism
History
A comprehensive history is also mandatory in the diagnosis
of non-ischaemic priapism and follows the same principles as
described in Table 1.
Recommendations for the diagnosis of non-ischaemic

priapism
The same recommendations as for ischaemic priapism apply.
Disease Management

non-ischaemic priapism
Because non-ischaemic priapism is not an Weak
emergency, perform definitive management
at the discretion of the treating physician.
Manage conservatively with the use of site Weak
specific perineal compression as the first
step, especially in children. Consider
androgen deprivation therapy only in adults.
Perform superselective arterial Strong
embolisation, using temporary material.
Repeat the procedure with temporary or Weak
permanent material for recurrent non-
ischaemic priapism following selective
arterial embolisation.
Reserve selective surgical ligation of a Weak
fistula as a final treatment option when
embolisation has failed.
Priapism 215
Stuttering (Recurrent or Intermittent) Priapism
History
A comprehensive history is mandatory and follows the same
principles as described in Table 1.
Disease Management

stuttering priapism
Manage each acute episode similar to that Weak
for ischaemic priapism.
Use hormonal therapies (mainly Weak
gonadotropin-receptor hormone agonists
or antagonists) and/or anti-androgens
for the prevention of future episodes in
patients with frequent relapses. Do not use
them before sexual maturation is reached.
Initiate treatment with phosphodiesterase Strong
type 5 inhibitors only when the penis is in
its flaccid state.
Use digoxin, α-adrenergic agonists, baclofen, Weak
gabapentin or terbutaline only in patients
with very frequent and uncontrolled relapses.
Use intracavernous self-injections at home Weak
of sympathomimetic drugs for the treatment
of acute episodes on an interim basis until
ischaemic priapism has been alleviated.

216 Priapism
EAU GUIDELINES ON
PENILE CURVATURE

Introduction
Congenital penile curvature results from disproportionate
development of the tunica albuginea of the corporal bodies
and is not associated with urethral malformation. In the
majority of the cases the curvature is ventral but, can be
lateral though rarely dorsal.
Taking a medical and sexual history is usually sufficient
to establish the diagnosis of congenital penile curvature.
Patients usually present after reaching puberty as the
curvature becomes more apparent with erections, and severe
curvature can make intercourse difficult or impossible.
Physical examination during erection (autophotograph or
after intracavernosal injection of vasoactive drugs) is useful
to document curvature and exclude other pathologies.
Disease management
The treatment of this disorder is surgical correction deferred
until after puberty. Surgical treatments for congenital penile
curvature generally share the same principles as in Peyronie’s
disease (presented in detail in the next section). Nesbit proce-
dure with excision of an ellipse of the tunica albuginea is the
gold standard of treatment but many other techniques have
Penile Curvature 217

been described and employed. Plication techniques are widely
used including techniques producing a de-rotation of the
corporal bodies. Most of the time, dissection and mobilisation
of the penile dorsal neurovascular bundle are required in order
to avoid loss of sensation and ischaemia to the glans penis.
Peyronie’s disease
An insult (repetitive microvascular injury or trauma) to the
tunica albuginea is the most widely accepted hypothesis
on the aetiology of the disease. A prolonged inflammatory
response will result in the remodelling of connective tissue
into a fibrotic plaque. Penile plaque formation can result in
curvature which, if severe, may prevent vaginal intromission.
The most commonly associated comorbidities and risk

factors are diabetes, hypertension, lipid abnormalities,
ischaemic cardiopathy, erectile dysfunction (ED), smoking,
and excessive consumption of alcohol.
Two phases of the disease can be distinguished. The first is

the acute inflammatory phase, which may be associated with
pain in the flaccid state or painful erections and a palpable
nodule or plaque in the tunica of the penis; typically a penile
curvature begins to develop. The second is the fibrotic phase
with the formation of hard palpable plaques that can be
calcified, which also results in disease stabilisation.
The aim of the initial evaluation is to provide information on
the presenting symptoms and their duration (erectile pain,
palpable nodules, curvature, length, rigidity, and girth) and
erectile function status. It is mandatory to obtain information
on the distress provoked by the symptoms and the potential
risk factors for ED and Peyronie’s disease.
218 Penile Curvature

Major attention should be given to whether the disease is still
active, as this will influence medical treatment or the timing of
surgery. Patients who are still likely to have an active disease
are those with short symptom duration, pain during erection,
or a recent change in penile curvature.
The examination should start with a routine genito-urinary

assessment, which is then extended to the hands and feet for
detecting possible Dupuytren’s contracture or Ledderhose
scarring of the plantar fascia. Penile examination consists
generally of a palpable node or plaque. The extent of curvature
must be evaluated with self-photograph, vacuum-assisted
erection test or pharmacological-induced erection test.
Measurement of length during erection is important because
it may have an impact on treatment decisions.
Erectile dysfunction is common in patients with Peyronie’s

disease (> 50%) but it is important to define whether it pre- or
post-dates the onset of Peyronie’s disease.

evaluation of Peyronie’s disease
In the medical and sexual history of patients Strong
with Peyronie’s disease, include duration of
the disease, penile pain, change of penile
deformity, difficulty in vaginal intromission
due to deformity, and erectile dysfunction
(ED).
In the physical examination, include Strong
assessment of palpable plaques, penile
length, extent of curvature (self-photograph,
vacuum-assisted erection test or pharma-
cological-induced erection) and any other
possibly related diseases (Dupuytren’s
contracture, Ledderhose disease).

Do not use Peyronie’s disease specific Weak
questionnaire in everyday clinical practice.
Do not use ultrasound (US) measurement Weak
of plaque size in everyday clinical practice.
Use Doppler US only in the case of Weak
diagnostic evaluation of ED, to ascertain
vascular parameters associated with ED.
Disease management
Non-operative treatment
Clostridium collagenase is the only drug approved for the
treatment of Peyronie’s disease by the FDA. No single drug has
been approved by the European Medicines Agency (EMA) for
the treatment of Peyronie’s disease at this time.
Table 1: Non-operative treatments for Peyronie’s disease
Oral treatments
Vitamin E
Potassium para-aminobenzoate (Potaba)
Tamoxifen
Colchicine
Acetyl esters of carnitine
Pentoxifylline
Phosphodiesterase type 5 inhibitors
Intralesional treatments
Steroids
Verapamil
Clostridium collagenase
Interferon

Topical treatments
Verapamil
Iontophoresis
H-100 gel
Extracorporeal shockwave treatment
Traction devices
Recommendations for the non-operative Strength rating

treatment of Peyronie’s disease
Use conservative treatment in patients Weak
not fit for surgery or when surgery is not
acceptable to the patient.
Do not use extracorporeal shockwave Weak
treatment to improve penile curvature and
reduce plaque size.
Use penile traction devices and vacuum Weak
devices to reduce penile deformity and
increase penile length.
Do not use intralesional treatment with Weak
steroids to reduce penile curvature, plaque
size or pain.
Do not use oral treatment with vitamin E Weak
and tamoxifen for significant reduction in
penile curvature or plaque size.
Do not offer other oral treatments Weak
(acetyl esters of carnitine, pentoxifylline,
colchicine).

Surgical treatment

Perform surgery only when Peyronie’s Strong
disease has been stable for at least three
months (without pain or deformity
deterioration), which is usually the case
after twelve months from the onset of
symptoms, and intercourse is compromised
due to deformity.
Prior to surgery, assess penile length, Strong
curvature severity, erectile function
(including response to pharmacotherapy in
case of ED) and patient expectations.
Use tunical shortening procedures, Strong
especially plication techniques as the first
treatment option for congenital penile
curvature and for Peyronie’s disease with
adequate penile length, curvature < 60° and
absence of special deformities (hour-glass,
hinge).
Use grafting techniques for patients with Weak
Peyronie’s disease and normal erectile
function, with no adequate penile length,
curvature > 60º and presence of special
deformities (hour-glass, hinge).
Use penile prosthesis implantation, with or Strong
without any additional procedure (model-
ling, plication or grafting), in Peyronie’s
disease patients with ED not responding to
pharmacotherapy.

Table 2: Types of grafts used in Peyronie’s disease surgery
Autologous grafts
Dermis
Vein grafts
Tunica albuginea
Tunica vaginalis
Temporalis fascia
Buccal mucosa
Allografts
Cadaveric pericardium
Cadaveric fascia lata
Cadaveric dura matter
Cadaveric dermis
Xenografts
Porcine small intestinal submucosa
Bovine pericardium
Porcine dermis
Synthetic grafts
Gore-Tex®
Dacron®
Collagen fleece (TachoSil®)

Figure 1: Treatment algorithm for Peyronie’s disease
Treatment of Peyronie’s disease
Discuss natural history of the disease

Reassure paent that Peyronie’s is a benign disease
Discuss current treatment modalies
Shared decision-making
Ac ve disease Stable disease

(pain, deformity deterioraon, (no pain, no deformity
no calcificaon on US) deterioraon, calcificaon
plaques on US)
Curvature < 30° Curvature > 30°

Conservave treatment No severe deformity Severe deformity
(hour-glass, hinge
No ED ED
No further treatment Surgical treatment
ED = erectile dysfunction; US = Ultrasound.


EAU GUIDELINES ON MALE
INFERTILITY
A. Jungwirth (Chair), T. Diemer (Vice-Chair), Z. Kopa, C. Krausz,

S. Minhas, H. Tournaye
Introduction
‘Infertility is the inability of a sexually active,
non-contracepting couple to achieve spontaneous pregnancy
in one year.’ (World Health Organization 2000).
Epidemiology and aetiology

About 15% of couples do not achieve pregnancy within one
year and seek medical treatment for infertility.
Male fertility can be impaired as a result of:

• congenital or acquired urogenital abnormalities;
• malignancies;
• urogenital tract infections;
• increased scrotal temperature (e.g. as a consequence of
varicocele);
• endocrine disturbances;
• genetic abnormalities;
• immunological factors.
Prognostic factors
The main factors influencing the prognosis in infertility are:
• duration of infertility;
• primary or secondary infertility;
• results of semen analysis;
• age and fertility status of the female partner.
Male Infertility 225

The diagnosis of male fertility should focus on a number of
prevalent disorders (Table 1). Simultaneous assessment of the
female partner is preferable, even if abnormalities are found in
the male, since data show that in one out of four couples both
male and female partners have pathological findings.
Semen analysis
A comprehensive andrological examination is indicated if
semen analysis shows abnormalities compared with reference
values (Table 1).
226 Male Infertility

Table 1: Lower reference limits (5th centiles and their 95%
CIs) for semen characteristics
Parameter Lower reference

limit (range)
Semen volume (mL) 1.5 (1.4-1.7)
Total sperm number (106/ejaculate) 39 (33-46)
Sperm concentration (106/mL) 15 (12-16)
Total motility (PR + NP) 40 (38-42)
Progressive motility (PR, %) 32 (31-34)
Vitality (live spermatozoa, %) 58 (55-63)
Sperm morphology (normal forms, %) 4 (3.0-4.0)
Other consensus threshold values
pH > 7.2
Peroxidase-positive leukocytes (106/mL) < 1.0
Optional investigations
MAR test (motile spermatozoa with < 50
bound particles, %)
Immunobead test (motile spermatozoa < 50
with bound beads, %)
Seminal zinc (μmol/ejaculate) ≥ 2.4
Seminal fructose (μmol/ejaculate) ≥ 13
Seminal neutral glucosidase ≤ 20
(mU/ejaculate)

Include the fertility status of the female Strong
partner in the diagnosis and management
of male sub-fertility because this might
determine the final outcome.
Perform semen analyses according to the Strong
guidelines of the WHO Laboratory Manual
for the Examination and Processing of
Human Semen (5th edn).
Perform further andrological assessment Strong
when semen analysis is abnormal in at
least two tests.
Adhere to the 2000 WHO Manual for the Weak
standardised investigation, diagnosis and
management of the infertile male for diag-
nosis and evaluation of male sub-fertility.
Primary Spermatogenic Failure
Routine investigations include semen analysis and hormonal
determinations. Other investigations may be required
depending on the individual situation.
Semen analysis
In non-obstructive azoospermia (NOA), semen analysis shows
normal ejaculate volume and azoospermia after centrifuga-
tion. A recommended method is semen centrifugation at
3000 g for 15 minutes and a thorough microscopic
examination by phase contrast optics at x 200 magnification
of the pellet. All samples can be stained and re-examined
microscopically.

Hormonal determinations
In men with testicular deficiency, hypergonadotropic hypo-
gonadism is usually present, with elevated levels of follicle
stimulating hormone (FSH) and luteinising hormone (LH),
and with or without low levels of testosterone. Generally, the
levels of FSH correlate with the number of spermatogonia
and are elevated when spermatogonia are absent or markedly
diminished. Spermatogenic arrest is typically associated with
normal FSH.
Testicular biopsy
Testicular biopsy and simultaneous testicular sperm
extraction (TESE) is a therapeutic option in couples
considering assisted reproductive techniques (ART) in men
with NOA.

For men who are candidates for sperm Strong
retrieval, give appropriate genetic counsel-
ling even when testing for genetic
abnormalities was negative.
Perform multiple testicular biopsies Strong
(TESE or micro-TESE) in men with non-
obstructive azoospermia, to define
spermatogenesis, cryopreserve sperm and
diagnose germ cell neoplasia in situ.
Genetic Disorders in Infertility

Current routine clinical practice is based on the screening
of genomic DNA from peripheral blood samples, however,
screening of chromosomal anomalies in spermatozoa is also
feasible and can be performed in selected cases.

Obtain standard karyotype analysis in all Strong
men with damaged spermatogenesis (sper-
matozoa < 10 million/mL) for diagnostic
purposes.
Provide genetic counselling in all couples Strong
with a genetic abnormality found on clinical
or genetic investigation and in patients who
carry a (potential) inheritable disease.
For all men with Klinefelter’s syndrome, Strong
provide long-term endocrine follow-up
and appropriate medical treatment, if
necessary.
Do not test for microdeletions in men with Strong
obstructive azoospermia (OA) since
spermatogenesis should be normal.
Inform men with Yq microdeletion and Strong
their partners who wish to proceed with
intracytoplasmic sperm injection that
microdeletions will be passed to sons, but
not to daughters.
In men with structural abnormalities of the Strong
vas deferens (unilateral or bilateral absence
with no renal agenesis), test the man and
his partner for cystic fibrosis transmem-
brane conductance regulator gene
mutations.
Obstructive Azoospermia
Obstructive azoospermia (OA) is the absence of spermatozoa
and spermatogenetic cells in semen and post-ejaculate urine
due to obstruction. Sometimes, the vas deferens is absent as
in Congenital Bilateral Absence of the Vas Deferens (CBAVD)
or Congenital Unilateral Absence of the Vas Deferens (CUAVD).

Obstruction in primary infertile men is frequently present at
the epididymal level.
Clinical examination should follow the investigation and
diagnostic evaluation of infertile men. The following findings
indicate OA:
• at least one testis with a volume > 15 mL, although a
smaller volume may be found in some patients with OA
and concomitant partial testicular failure;
• enlarged and dilated epididymis;
• nodules in the epididymis or vas deferens;
• absence or partial atresia of the vas.
Semen analysis
At least two examinations must be carried out at an interval
of one to two months, according to the WHO. When semen
volume is low, a search must be made for spermatozoa in
urine after ejaculation. Absence of spermatozoa and
immature germ cells in semen smears suggest complete
seminal duct obstruction.
Hormone levels
Serum FSH and Inhibin B levels may be normal, but do not
exclude a testicular cause of azoospermia (e.g. spermatogenic
arrest).
Ultrasonography
In addition to physical examination, a scrotal ultrasound may
be helpful in finding signs of obstruction (e.g. dilatation of rete
testis, enlarged epididymis with cystic lesions, or absent vas
deferens) and may demonstrate signs of testicular dysgenesis
(e.g., non-homogeneous testicular architecture and
microcalcifications) or testis tumours.

Testicular biopsy
In selected cases, testicular biopsy is indicated to exclude
spermatogenic failure. Testicular biopsy should be combined
with extraction of testicular spermatozoa (i.e. TESE) for
cryopreservation.

Perform microsurgical vasovasostomy or Strong
tubulovasostomy for azoospermia caused
by vasal or epididymal obstruction.
Use sperm retrieval techniques, such Strong
as microsurgical epididymal sperm
aspiration, testicular sperm extraction and
percutaneous epididymal sperm aspiration
only when facilities for cryostorage are
available.
Varicocele
Varicocele is a common genital abnormality which may be
associated with the following andrological conditions:
• failure of ipsilateral testicular growth and development;
• symptoms of pain and discomfort;
• male sub-fertility;
• hypogonadism.
The diagnosis of varicocele is made by clinical examination
and should be confirmed by colour Duplex analysis. In centres
where treatment is carried out by antegrade or retrograde
sclerotherapy or embolisation, diagnosis is additionally
confirmed by X-ray.
Disease management
Several treatments are available for varicoceles. Current
evidence indicates that microsurgical varicocelectomy is the

most effective with the lowest complication rate among the
varicocelectomy techniques.

Treat varicoceles in adolescents with Weak
ipsilateral reduction in testicular volume
and evidence of progressive testicular
dysfunction.
Do not treat varicoceles in infertile men Strong
who have normal semen analysis and in
men with a subclinical varicocele.
Treat men with a clinical varicocele, oligo- Weak
zoospermia and otherwise unexplained
infertility in the couple.
Hypogonadism
Idiopathic hypogonadotropic hypogonadism

Idiopathic hypogonadotropic hypogonadism is characterised
by low levels of gonadotropins and sex steroid in the absence
of anatomical or functional abnormalities of the
hypothalamic-pituitary-gonadal axis. Stimulation of sperm
production requires treatment with human chorionic
gonadotropin (hCG) combined with recombinant FSH or
urinary FSH or human menopausal gonadotropins (hMGs).
Hypergonadotropic hypogonadism
Many conditions in men are associated with hypergonado-
tropic hypogonadism and impaired fertility (e.g. anorchia,
maldescended testes, Klinefelter’s syndrome, trauma, orchitis,
systemic diseases, testicular tumour, varicocele etc).

Provide testosterone replacement therapy Strong
for symptomatic patients with primary and
secondary hypogonadism who are not
considering parenthood.
In men with hypogonadotropic hypo- Strong
gonadism, induce spermatogenesis by an
effective drug therapy (human chorionic
gonadotropin, human menopausal
gonadotropins, recombinant follicle-
stimulating hormone (rFSH), highly purified
FSH (hpFSH)).
Do not use testosterone replacement for Strong
the treatment of male infertility.
Cryptorchidism
The aetiology of cryptorchidism is multifactorial, involving
disrupted endocrine regulation and several gene defects. It
has been postulated that cryptorchidism may be a part of the
so-called testicular dysgenesis syndrome (TDS), which is a
developmental disorder of the gonads caused by
environmental and/or genetic influences early in pregnancy.
Besides cryptorchidism, TDS may include hypospadias,
reduced fertility, increased risk of malignancy, and Leydig cell
dysfunction.

Do not use hormonal treatment of Strong
cryptorchidism in adults.
If undescended testes are corrected in Weak
adulthood, perform simultaneous testicular
biopsy for detection of intratubular germ
cell neoplasia in situ (formerly carcinoma
in situ).
Provide medical treatment for male Strong
infertility in patients with of
hypogonadotropic hypogonadism.
No clear recommendation can be made Strong
for treatment of patients with idiopathic
infertility using gonadotropins,
anti-oestrogens, and antioxidants.

Male Contraception

Use cauterisation and fascial interposition Strong
as they are the most effective techniques
for the prevention of early recanalisation.
Inform patients seeking vasectomy about Strong
the surgical technique, risk of failure,
potential irreversibility, the need for post-
procedure contraception until clearance,
and the risk of complications.
In order to achieve pregnancy, Weak
microsurgical epididymal sperm aspiration/
percutaneous epididymal sperm aspiration/
testicular sperm extraction - together
with intracytoplasmic sperm injection is a
second-line option for men who decline a
vasectomy reversal and those with failed
vasectomy reversal surgery.
Male Accessory Gland Infections and Infertility
Ejaculate analysis
Ejaculate analysis according to WHO criteria, might indicate
persistent inflammatory activity. It clarifies whether the
prostate is involved as part of a generalised male accessory
gland infection and provides information about sperm quality.

Microbiological findings
After exclusion of urethritis and bladder infection, >106
peroxidase-positive white blood cells (WBCs) per millilitre
of ejaculate indicate an inflammatory process. In this case,
a culture should be performed for common urinary tract
pathogens.
Disease management
Antibiotic therapy is not indicated before culture results are
available.

Instruct patients with epididymitis that is Strong
known or suspected to be caused by
N. gonorrhoeae or C. trachomatis to refer
their sexual partners for evaluation and
treatment.

Germ Cell Malignancy and Testicular Microcalcification
(TM)

Encourage men with testicular microcalci- Weak
fication (TM) to perform self-examination
even without additional risk factors as this
may result in early detection of testicular
germ cell tumour (TGCT).
Do not perform testicular biopsy, follow-up Strong
scrotal ultrasound, routine use of biochemi-
cal tumour markers, or abdominal or pelvic
computed tomography, in men with
isolated TM without associated risk factors
(e.g. infertility, cryptorchidism, testicular
cancer, and atrophic testis).
Perform testicular biopsy for men with TM, Strong
who belong to one of the following high-
risk groups: spermatogenic failure, bilateral
TM, atrophic testes (less than 12cc), history
of undescended testes and TGCT.
If there are suspicious findings on physical Strong
examination or ultrasound in patients with
TM and associated lesions, perform
surgical exploration with testicular biopsy
or orchidectomy.
Follow men with TGCT because they are at Strong
increased risk of developing hypogonadism
and sexual dysfunction.
Disorders of Ejaculation
Disorders of ejaculation are uncommon, but important causes
of male infertility.

Diagnostic management includes the following recommended
procedures:
• clinical history;
• physical examination;
• post-ejaculatory urinalysis;
• microbiological examination;
• optional diagnostic work-up.
This diagnostic work-up can include:

• neurophysiological tests (bulbocavernosus evoked
response and dorsal nerve somatosensory evoked
potentials);
• tests for autonomic neuropathy;
• psychosexual evaluation;
• videocystometry;
• cystoscopy;
• transrectal ultrasonography;
• uroflowmetry;
• vibratory stimulation of the penis.
Disease management
The following aspects must be considered when selecting
treatment:
• age of patient and his partner;
• psychological problems of the patient and his partner;
• couple’s willingness and acceptance of different fertility
procedures;
• associated pathology;
• psychosexual counselling.

Offer specific treatments for ejaculatory Strong
disorders before performing sperm collec-
tion and assisted reproduction technique.
Premature ejaculation can be treated
using dapoxetine (short acting selective
serotonin reuptake inhibitor) and/or topical
anaesthetics.

Semen cryopreservation

Offer cryopreservation of semen to all men Strong
who are candidates for chemotherapy,
radiation or surgical interventions that
might interfere with spermatogenesis or
cause ejaculatory disorders.
Offer simultaneous sperm cryopreservation Strong
if testicular biopsies will be performed for
fertility diagnosis.
If cryopreservation is not available locally, Strong
inform patients about the possibility of
visiting, or transferring to a
cryopreservation unit before therapy starts.
Take precautions to prevent Strong
transmission of viral, sexually transmitted
or any other infection by cryostored
materials from donor to recipient, and to
prevent contamination of stored samples.
These precautions include testing of the
patient and the use of rapid testing and
quarantine of samples until test results are
known. Do not store samples from men
who are positive for hepatitis virus or HIV in
the same container as samples from men
who have been tested and are free from
infection.

EAU Guidelines ISBN 978-94-92671-02-8), available to all members

EAU GUIDELINES ON
MALE HYPOGONADISM
G.R. Dohle (Chair), S. Arver, C. Bettocchi, T.H. Jones, S. Kliesch
Introduction
Male hypogonadism is a clinical syndrome caused by
androgen deficiency which may adversely affect multiple
organ functions and quality of life. Androgen deficiency
increases slightly with age. In middle-aged men the incidence
is 6%. Hypogonadism is more prevalent in older men, in men
with obesity, those with comorbidities, and in men with a poor
health status.
Aetiology and classification

Male hypogonadism can be classified in accordance with
disturbances at the level of:
• the testes (primary hypogonadism);
• the hypothalamus and pituitary (secondary
hypogonadism);
• the hypothalamus/pituitary and gonads (common in adult
onset hypogonadism);
• androgen target organs (androgen insensitivity/resistance).
242 Male Hypogonadism

Table 1: Most common forms of primary hypogonadism
Disease Pathophysiology
Maldescended or ectopic Failure of testicular descent,
testes maldevelopment of the testis
Klinefelter syndrome 47,XXY Sex-chromosomal non-
disjunction in germ cells
Germ Cell Tumour Testicular maldevelopment
Orchitis Viral or unspecific orchitis
Acquired anorchia Trauma, tumour, torsion,
inflammation, iatrogenic,
surgical removal
Secondary testicular Medication, drugs, toxins,
dysfunction systemic diseases
(Idiopathic) testicular Male infertility (idiopathic or
atrophy/testicular dysgenesis specific causes)
Congenital anorchia (bilateral Intra-uterine torsion is the
in 1 in 20,000 males, unilateral most probable cause
4 times as often)
Table 2: Most common forms of secondary hypogonadism
Disease Pathophysiology
Hyperprolactinemia Prolactin-secreting pituitary
adenomas (prolactinomas)
or drug-induced
Isolated (congenital) Specific (or unknown)
hypogonadotropic mutations affecting GnRH
hypogonadism (IHH/CHH) synthesis or action
(formerly termed idiopathic
hypogonadotropic
hypogonadism)
Male Hypogonadism 243

Kallmann’s syndrome GnRH deficiency and
(hypogonadotropic anosmia, genetically
hypogonadism with anosmia) determined
(prevalence 1 in 10,000)
Secondary GnRH deficiency Medication, drugs, toxins,
systemic diseases
Hypopituitarism Radiotherapy, trauma,
infections, haemo-
chromatosis and vascular
insufficiency or congenital
Pituitary adenomas Hormone-secreting
adenomas; hormone-inactive
pituitary adenomas;
metastases to the pituitary
or pituitary stalk

Differentiate the two forms of Strong
hypogonadism (primary and secondary
hypogonadism) by determining luteinising
hormone and follicle-stimulating hormone
levels, as this has implications for patient
evaluation and treatment and makes it
possible to identify patients with associated
health problems and infertility.

Table 3: Signs and symptoms suggesting prepubertal-onset

hypogonadism
Delayed puberty
Small testes
Cryptorchidism
Gynaecomastia
High-pitched voice
Unclosed epiphyses
Linear growth into adulthood
Eunuchoid habitus
Sparse body hair/facial hair
Infertility
Low bone mass
Sarcopenia
Reduced sexual desire/activity
Table 4: Signs and symptoms associated with adult-onset

hypogonadism
Loss of libido
Erectile dysfunction
Fewer and decreased morning erections
Overweight or obesity
Sarcopenia
Low bone mass
Depressive thoughts
Fatigue
Loss of body hair

Hot flushes
Loss of vigour
Recommendations for diagnostic Strength rating

evaluation
Restrict the diagnosis of testosterone Strong
deficiency to men with persistent symptoms
suggesting hypogonadism (Tables 3 and 4).
Measure testosterone in the morning Strong
before 11.00 hours, preferably in the fasting
state.
Repeat total testosterone on at least Strong
two occasions with a reliable method. In
addition, measure the free testosterone
level in men with:
- Total testosterone levels close to the
lower normal range (8-12 nmol/L), to
strengthen the laboratory assessment.
- Suspected or known abnormal sex
hormone-binding globulin levels.

Consider assessing testosterone in men Strong
with a disease or treatment in which
testosterone deficiency is common and in
whom treatment may be indicated.
This includes men with:
-S exual dysfunction.
-T ype 2 diabetes.
- Metabolic syndrome.
- Obesity.
-P ituitary mass, following radiation
involving the sellar region and other
diseases in the hypothalamic and sellar
region.
- Treatment with medications that cause
suppression of testosterone levels - e.g.
corticosteroids and opiates.
- Moderate to severe chronic obstructive
lung disease.
- Infertility.
- Osteoporosis or low-trauma fractures.
- HIV infection with sarcopenia.
Analyse LH and FSH serum levels to Strong
differentiate between primary and
secondary forms of hypogonadism.
HIV = human immunodeficiency virus;
LH = luteinizing hormone; FHS = follicle stimulating hormone.
Recommendations for screening men with Strength rating

adult-onset hypogonadism
Screen for testosterone deficiency only in Weak
adult men with consistent and multiple
signs and symptoms listed in Table 3.

Young men with testicular dysfunction Strong
and men older than 50 years of age with
low testosterone should additionally be
screened for osteoporosis.
Disease management
Table 5: Indications for testosterone treatment
Delayed puberty (constitutional or congenital forms

(hypogonadotropic hypogonadism, Kallmann’s syndrome))
Klinefelter syndrome with hypogonadism
Sexual dysfunction and low testosterone
Low bone mass in hypogonadism
Adult men with low testosterone and consistent and
preferably multiple signs and symptoms of hypogonadism
following unsuccessful treatment of obesity and
comorbidities (listed in Table 4)
Hypopituitarism
Table 6: Contraindications against testosterone treatment
Locally advanced or metastatic prostate cancer

Male breast cancer
Men with an active desire to have children
Haematocrit > 0.54%
Severe chronic cardiac failure/New York Heart Association
Class IV

Table 7: Testosterone preparations for replacement therapy
Formulation Administration Advantages Disadvantages

Testosterone Oral; 2-6 cps Absorbed Variable levels
undecanoate every 6 hours through the of testosterone
lymphatic above and
system, with below the mid-
consequent range. Need for
reduction of several doses
liver per day with
involvement. intake of fatty
food.
Testosterone Intramuscular; Short-acting Possible
cypionate one injection preparation fluctuation of
every two to that allows drug testosterone
three weeks withdrawal in levels.
case of onset of
side-effects.
Testosterone Intramuscular; Short-acting Fluctuation of
enanthate one injection preparation testosterone
every two to that allows drug levels.
three weeks withdrawal in
case of onset of
side-effects.
Testosterone Intramuscular; Steady-state Long-acting
undecanoate one injection testosterone preparation
every ten to levels without that cannot
fourteen weeks fluctuation. allow drug
withdrawal in
case of onset
of side-effects.

Transdermal Gel; daily Steady-state Risk of
testosterone application testosterone interpersonal
level without transfer.
fluctuation.
Subdermal Subdermal Long duration Risk of
depots implant every and constant infection and
five to seven serum testos- extrusion of
months terone level. the implants.
Recommendations for testosterone Strength rating

replacement therapy
Fully inform the patient about expected Strong
benefits and side-effects of the treatment
option. Select the preparation with a joint
decision by an informed patient and the
physician.
Use short-acting preparations rather than Weak
long-acting depot administration when
starting the initial treatment, so that
therapy can be adjusted or stopped in case
of adverse side-effects.
Do not use testosterone therapy in patients Strong
with male infertility or active child wish since
it may suppress spermatogenensis.
Only use human chorionic gonadotropin Strong
treatment for (hypogonadotrophic)
hypogonadal patients with simultaneous
fertility treatment.
In patients with adult-onset hypogonadism, Strong
only prescribe testosterone treatment in
men with multiple symptoms and if weight
loss, lifestyle modification and good
treatment balance of comorbidities have
proven unsuccessful.

Recommendations on risk factors in Strength rating
testosterone treatment
Perform haematological, cardiovascular, Strong
breast and prostatic assessment before the
start of treatment.
Monitor testosterone, haematocrit, Strong
haemoglobin and prostate-specific antigen
(PSA) during testosterone treatment.
Offer testosterone treatment cautiously in Weak
symptomatic hypogonadal men who have
been surgically treated for localised prostate
cancer and who are currently without
evidence of active disease (i.e. measurable
PSA, abnormal rectal examination, evidence
of bone/visceral metastasis): treatment
should be restricted to those patients with
a low risk for recurrent prostate cancer (i.e.
Gleason score < 8; pathological stage pT1-2;
pre-operative PSA < 10 ng/mL) and should
not start before one year of follow-up.
Assess for cardiovascular risk factors before Strong
commencing testosterone treatment and
optimise secondary prevention in men with
pre-existing cardiovascular disease.
Treat men with hypogonadism and either Strong
pre-existing cardiovascular disease, venous
thromboembolism or chronic cardiac failure
who require testosterone treatment with
caution by carefully monitoring with clinical
assessment, haematocrit (not exceeding
0.54%) and testosterone levels maintained
as best possible for age within the
mid-normal healthy range.

Assess the response to testosterone Strong
treatment at three, six and twelve months
after the onset of treatment, and thereafter
annually.
Monitor testosterone, haematocrit at three, Strong
six and twelve months and thereafter
annually. Decrease the testosterone dosage
or switch testosterone preparation from
intramuscular to topical or venesection, if
haematocrit is above 0.54%. If haematocrit
remains elevated, stop testosterone and
reintroduce at a lower dose once
haematocrit has normalised.
Assess prostate health by digital rectal Strong
examination and prostate-specific antigen
(PSA) before the start of testosterone
replacement therapy. Follow-up by PSA
tests at three, six and twelve months and
thereafter annually.
Assess men with cardiovascular diseases Strong
for cardiovascular symptoms before
testosterone treatment is initiated and
continue close clinical assessment during
treatment.


EAU GUIDELINES ON
UROLOGICAL INFECTIONS
G. Bonkat (Co-chair), R. Pickard (Co-chair), R. Bartoletti, T. Cai,

F. Bruyere, S.E. Geerlings, B. Köves, F. Wagenlehner
Guidelines Associates: A. Pilatz, B. Pradere, R. Veeratterapillay
Introduction
The European Association of Urology (EAU) Urological
Infections Guidelines Panel has compiled these clinical
guidelines to provide medical professionals with evidence-
based information and recommendations for the prevention
and treatment of urological tract infections (UTIs). These
guidelines also aim to address the important public health
aspects of infection control and antimicrobial stewardship.
Antimicrobial Stewardship
Stewardship programs have two main sets of actions. The
first set mandates use of recommended care at the patient
level conforming to guidelines. The second set describes
strategies to achieve adherence to the mandated guidance.
These include persuasive actions such as education and
feedback together with restricting availability linked to local
formularies. The important components of antimicrobial
stewardship programs are:
• regular training of staff in best use of antimicrobial agents;
• adherence to local, national or international guidelines;
• regular ward visits and consultation with infectious
diseases physicians and clinical microbiologists;
• audit of adherence and treatment outcomes;
• regular monitoring and feedback to prescribers of their
performance and local pathogen resistance profiles.
Urological Infections 253

Asymptomatic Bacteriuria
Asymptomatic bacteriuria in an individual without urinary
tract symptoms is defined by a mid-stream sample of urine
showing bacterial growth ≥ 105 cfu/mL in two consecutive
samples in women and in one single sample in men.

Do not screen or treat asymptomatic
bacteriuria in the following conditions:
• women without risk factors; Strong
• patients with well-regulated diabetes Strong
mellitus;
• post-menopausal women; Strong
• elderly institutionalised patients; Strong
• patients with dysfunctional and/or Strong
reconstructed lower urinary tracts;
• patients with renal transplants; Strong
• patients prior to arthoplasty surgeries; Strong
• patients with recurrent urinary tract Strong
infections.
Screen for and treat asymptomatic Strong
bacteriuria prior to urological procedures
breaching the mucosa.
Screen for and treat asymptomatic Weak
bacteriuria in pregnant women with
standard short course treatment.
Uncomplicated Cystitis
Uncomplicated cystitis is defined as acute, sporadic or
recurrent cystitis limited to non-pregnant, pre-menopausal
women with no known relevant anatomical and functional
abnormalities within the urinary tract or comorbidities.
254 Urological Infections

evaluation of uncomplicated cystitis
Diagnose uncomplicated cystitis in women Strong
who have no other risk factors for compli-
cated urinary tract infections based on:
• a focused history of lower urinary tract
symptoms (dysuria, frequency and
urgency);
• the absence of vaginal discharge or
irritation.
Use urine dipstick testing for diagnosis of Weak
acute uncomplicated cystitis.
Urine cultures should be done in the Strong
following situations:
• suspected acute pyelonephritis;
• symptoms that do not resolve or recur
within four weeks after the completion
of treatment;
• women who present with atypical
symptoms;
• pregnant women.
Recommendations for antimicrobial Strength rating

therapy for uncomplicated cystitis
Prescribe fosfomycin trometamol, Strong
pivmecillinam or nitrofurantoin as first-line
treatment for uncomplicated cystitis in
women.
Do not use aminopenicillins or Strong
fluoroquinolones to treat uncomplicated
cyctitis.

Table 1: Suggested regimens for antimicrobial therapy in
uncomplicated cystitis
Antimicrobial Daily dose Duration Comments
of
therapy
First-line women
Fosfomycin 3 g SD 1 day Recommended
trometamol only in women with
Nitrofurantoin 50-100 mg 5 days uncomplicated
macrocrystal four times cystitis.
a day
Nitrofurantoin 100 mg b.i.d 5 days
monohydrate/
macrocrystals
Nitrofurantoin 100 mg b.i.d 5 days
macrocrystal
prolonged release
Pivmecillinam 200 mg t.i.d 3-5 days
Alternatives
Cephalosporins 500 mg b.i.d 3 days Or comparable
(e.g. cefadroxil)
If the local resistance pattern for E. coli is < 20%
Trimethoprim 200 mg b.i.d 5 days Not in the first
trimenon of
pregnancy
Trimethoprim- 160/800 mg 3 days Not in the last
sulphamethoxazole b.i.d trimenon of
pregnancy
Treatment in men
Trimethoprim- 160/800 mg 7 days Restricted to men,
sulphamethoxazole b.i.d fluoroquinolones
can also be
prescribed in
accordance with
local susceptibility
testing.
SD = single dose; b.i.d = twice daily; t.i.d = three times daily.

Recurrent UTIs
Recurrent UTIs (rUTIs) are recurrences of uncomplicated
and/or complicated UTIs, with a frequency of at least three
UTIs/year or two UTIs in the last six months.

evaluation and treatment of rUTIs
Diagnose recurrent UTI by urine culture. Strong
Do not perform an extensive routine Weak
workup (e.g cystoscopy, full abdominal
ultrasound) in women younger than 40
years of age with recurrent UTI and no risk
factors.
Advise patients on behavioural Weak
modifications which might reduce the risk
of recurrent UTI.
Use vaginal oestrogen replacement in post- Weak
menopausal women to prevent recurrent
UTI.
Use immunoactive prophylaxis to reduce Strong
recurrent UTI in all age groups.
Use continuous or post-coital antimicrobial Strong
prophylaxis to prevent recurrent UTI when
non-antimicrobial interventions have failed.
Counsel patients regarding possible side
effects.
For patients with good compliance self- Strong
administered short term antimicrobial
therapy should be considered.

Uncomplicated Pyelonephritis
Uncomplicated pyelonephritis is defined as pyelonephritis
limited to non-pregnant, pre-menopausal women with no
known relevant urological abnormalities or comorbidities.

evaluation of uncomplicated pyelonephritis
Perform urinalysis (e.g. using a dipstick Strong
method), including the assessment of
white and red blood cells and nitrite, for
routine diagnosis.
Perform urine culture and antimicrobial Strong
susceptibility testing in patients with
pyelonephritis.
Perform imaging of the urinary tract to Strong
exclude urgent urological disorders.

uncomplicated pyelonephritis
Treat patients with uncomplicated pyelo- Strong
nephritis not requiring hospitalisation with
short course fluoroquinolones as first-line
treatment.
Treat patients with uncomplicated pyelo- Strong
nephritis requiring hospitalisation with an
intravenous antimicrobial regimen initially.
Switch patients initially treated with Strong
parenteral therapy, who improve clinically
and can tolerate oral fluids, to oral
antimicrobial therapy.
Do not use nitrofurantoin, fosfomycin, Strong
and pivmecillinam to treat uncomplicated
pyelonephritis.

Table 2: Suggested regimens for empirical oral antimicrobial
therapy in uncomplicated pyelonephritis
of
therapy
Ciprofloxacin 500-750 mg 7 days Fluoroquinolone
b.i.d resistance should
Levofloxacin 750 mg q.d 5 days be less than 10
percent.
Trimethoprim 160/800 mg 14 days If such agents are
sulphamethoxazol b.i.d used empirically, an
initial intravenous
Cefpodoxime 200 mg b.i.d 10 days dose of a long-
acting parenteral
antimicrobial (e.g.
Ceftibuten 400 mg q.d 10 days
ceftriaxone) should
be administered.
b.i.d = twice daily; q.d = every day.

Table 3: Suggested regimens for empirical parenteral
antimicrobial therapy in uncomplicated pyelonephritis
Antimicrobial Daily dose Comments
First-line treatment
Ciprofloxacin 400 mg b.i.d
Levofloxacin 750 mg q.d
Cefotaxime 2 g t.i.d Not studied as monotherapy
in acute uncomplicated
pyelonephritis.
Ceftriaxone 1-2 g q.d Lower dose studied, but
higher dose recommended.
Cefepime 1-2 g b.i.d Lower dose studied, but
Piperacillin/ 2.5-4.5 g t.i.d higher dose recommended.
tazobactam
Ceftolozane/ 1.5 g t.i.d
tazobactam
Ceftazidime/ 2.5 g t.i.d
avibactam
Gentamicin 5 mg/kg q.d Not studied as monotherapy
Amikacin 15 mg/kg q.d in acute uncomplicated
pyelonephritis.
Alternatives
Imipenem/ 0.5 g t.i.d Consider carbapenems only
cilastatin in patients with early culture
Meropenem 1 g t.i.d results indicating the
presence of multi-drug
resistance organisms.
b.i.d = twice daily; t.i.d = three times daily; q.d = every day.
Complicated UTIs
A complicated UTI (cUTI) occurs in an individual in whom
factors related to the host (e.g. underlying diabetes or
immunosuppression) or specific anatomical or functional
abnormalities related to the urinary tract (e.g. obstruction,
incomplete voiding due to detrusor muscle dysfunction) are

believed to result in an infection that will be more difficult to
eradicate than an uncomplicated infection.

complicated UTIs
Use the combination of: Strong
• amoxicillin plus an aminoglycoside;
• a second generation cephalosporin
plus an aminoglycoside;
• a third generation cephalosporin
intravenously as empirical treatment
of complicated UTI with systemic
symptoms.
Only use ciprofloxacin provided that the Strong
local resistance percentages are < 10%
when:
• the entire treatment is given orally;
• patients do not require hospitalisation;
• patient has an anaphylaxis for beta-
lactam antimicrobials.
Do not use ciprofloxacin and other Strong
fluoroquinolones for the empirical
treatment of complicated UTI in patients
from the urology department or when
patients have used fluoroquinolones in
the last six months.
Manage any urological abnormality and/or Strong
underlying complicating factors.
Catheter-associated UTIs
Catheter-associated UTI refers to UTIs occurring in a person
whose urinary tract is currently catheterised or has been
catheterised within the past 48 hours.

Recommendations for diagnostic Strength rating
evaluation of CA-UTI
Do not carry out routine urine culture in Strong
asymptomatic catheterised patients.
Do not use pyuria as an indicator for Strong
catheter-associated UTI.
Do not use the presence or absence of Strong
odorous or cloudy urine alone to differen-
tiate catheter-associated asymptomatic
bacteriuria from catheter-associated UTI.
Recommendations for disease Strength rating

management and prevention of CA-UTI
Treat symptomatic CA-UTI according to the Strong
recommendations for complicated UTIs.
Take a urine culture prior to initiating anti- Strong
microbial therapy in catheterised patients
in whom the catheter has been removed.
Do not treat catheter-associated Strong
asymptomatic bacteriuria in general.
Treat catheter-associated asymptomatic Strong
bacteriuria prior to traumatic urinary tract
interventions (e.g. transurethral resection
of the prostate).
Replace or remove the indwelling catheter Strong
before starting antimicrobial therapy.
Do not apply topical antiseptics or anti- Strong
microbials to the catheter, urethra or meatus.
Do not use prophylactic antimicrobials to Strong
prevent catheter-associated UTIs.
The duration of catheterisation should be Strong
minimal.

Recommendations for antibiotic Strength rating
prophylaxis following indwelling balder
catheter removal
Do not use antibiotic prophylaxis routinely Weak
to prevent clinical UTI after urethral
catheter removal.
Urosepsis
Urosepsis is defined as life threatening organ dysfunction
caused by a dysregulated host response to infection
originating from the urinary tract and/or male genital organs.

treatment of urosepsis
Perform the quickSOFA score to identify Strong
patients with potential sepsis.
Take a urine culture and two sets of blood Strong
cultures before starting antimicrobial
treatment.
Administer parenteral high dose broad Strong
spectrum antimicrobials within the first
hour after clinical assumption of sepsis.
Adapt initial empiric antimicrobial therapy Strong
on the basis of culture results.
Remove foreign bodies from and Strong
obstruction of the urinary tract.
Provide immediate adequate life-support Strong
measures.

Table 4: Suggested regimens for antimicrobial therapy for
urosepsis
Antimicrobials Daily dose Duration of therapy
Cefotaxime 2 g t.i.d 7-10 days
Ceftazidime 1-2 g t.i.d Longer courses are
appropriate in patients
Ceftriaxone 1-2 g q.d
who have a slow clinical
Cefepime 2 g b.i.d response
Piperacillin/tazobactam 4.5 g t.i.d
Ceftolozane/tazobactam 1.5 g t.i.d
Ceftazidime/avibactam 2.5 g t.i.d
Gentamicin* 5 mg/kg q.d
Amikacin* 15 mg/kg q.d
Ertapenem 1 g q.d
Imipenem/cilastatin 0.5 g t.i.d
Meropenem 1 g t.i.d
* Not studied as monotherapy in urosepsis
Urethritis
Inflammation of the urethra usually presents with LUTS and
must be distinguished from other infections of the lower
urinary tract. The following recommendations are based on
a review of several European national guidelines and are
aligned with the Center for Disease Control and Prevention’s
guidelines on sexual transmitted diseases.

evaluation and antimicrobial treatment of
urethritis
Perform a gram stain of urethral discharge Strong
or a urethral smear to preliminarily
diagnose pyogenic urethritis.

Perform a validated nucleic acid Strong
amplification tests on a mid-stream urine
sample or urethral smear to diagnosis
chlamydial and gonococcal infections.
Use a pathogen directed treatment based Strong
on local resistance data.

urethritis
Pathogen Antimicrobial Dosage & Alternative
Duration regimens
of
therapy
Gonococcal Ceftriaxone 1 g i.m., Cefixime
Infection SD 400 mg p.o., SD
Azithromycin 1-1.5 g Or
p.o., SD Azithromycin
1-1.5 g p.o., SD
Cefixime 800 mg
p.o., SD
Non-Gonococcal Doxycycline 100 mg Azithromycin
infection b.i.d, p.o., 0.5 g p.o., day 1,
(non-identified 7-10 days 250 mg p.o., day 2-5
pathogen)
Chlamydia Azithromycin 1.0-1.5 g Doxycycline
trachomatis p.o., SD 100 mg b.i.d, p.o., for
7 days
Mycoplasma Azithromycin 0.5 g p.o., Moxifloxacin 400
genitalium day 1, mg q.d., 5 days
250 mg however, because
p.o., day of reported failures,
2-5 some experts
recommend 10 -14
days

Ureaplasma Doxycycline 100 mg Azithromycin 1.0-1.5
urealiticum b.i.d, p.o., g p.o., single dose
7 days Or
clarithromycin 500
mg b.i.d, 7 days
(resistance against
macrolides is
possible)
Trichomonas Metronidazole 2 g p.o., Not in the last
vaginalis SD trimenon of
pregnancy
SD = single dose; b.i.d = twice daily; q.d = everyday; p.o. = orally,
i.m. = intramuscular.
Bacterial Prostatitis
Bacterial prostatitis is a clinical condition caused by bacterial
pathogens. It is recommended that urologists use the
classification suggested by the National Institute of Diabetes,
Digestive and Kidney Diseases of the National Institutes
of Health, in which bacterial prostatitis, with confirmed or
suspected infection, is distinguished from chronic pelvic pain
syndrome.

bacterial prostatitis
Perform a gentle digital rectal examination Weak
to assess the condition of the prostate.
Take a mid-stream urine dipstick to Weak
check nitrite and leukocytes in patients
with clinical suspicion of acute bacterial
prostatitis.
Take a blood culture and a total blood Weak
count in case of prostatitis-related
symptoms with malaise and fever.

Take a mid-stream urine culture in patients Weak
with acute prostatitis-related symptoms
to guide diagnosis and plan adequate
targeted antibiotic treatment.
Perform accurate microbiological Weak
evaluation for atypical pathogens such as
Chlamydia trachomatis or Mycoplasmata
in patients with chronic bacterial prostatitis
(CBP).
Perform the Meares and Stamey 2- or Strong
4-glass test in patients with CBP.
Preform transrectal ultrasound in selected Weak
cases to rule out the presence of prostatic
abscess, calcification in the prostate and
dilatation of the seminal vesicles.
Do not routinely perform microbiological Weak
analysis of the ejaculate alone to diagnosis
CBP.
Recommendations for the disease Strength rating

management of bacterial prostatitis
Acute bacterial prostatitis
Treat acute bacterial prostatitis according Strong
to the recommendations for complicated
UTIs.
Chronic bacterial prostatitis (CBP)
Prescribe a fluoroquinolone (e.g. Strong
ciprofloxacin, levofloxacin) as first-line
treatment for CBP.

Prescribe a macrolide (e.g. azithromycin) Strong
or a tetracycline (e.g. doxycycline) if
intracellular bacteria have been identified
as the causative agent of CBP.
Prescribe metronidazole in patients with Strong
Trichomonas vaginalis CBP.
Table 6: Suggested regimens for antimicrobial therapy for chronic

bacterial prostatitis
of
therapy
Floroquinolone Optimal 4-6
oral daily weeks
dose
Doxycycline 100 mg b.i.d 10 days Only for
C. trachomatis
or mycoplasma
infections.
Azithromycin 500 mg 3 weeks Only for
3x weekly C. trachomatis
infections
Metronidazole 500 mg t.i.d. 14 days Only for T. vaginalis
infections
Acute Infective Epididymitis

Acute epididymitis is clinically characterised by pain,
swelling and increased temperature of the epididymis, which
may involve the testis and scrotal skin. It is generally caused
by migration of pathogens from the urethra or bladder.
Torsion of the spermatic cord (testicular torsion) is the most
important differential diagnosis in boys and young men.

treatment of acute infective epididymitis
Obtain a mid-stream urine and first voided Strong
urine for pathogen identification by culture
and nucleic acid amplification test.
Initially prescribe a single antibiotic or Strong
a combination of two antibiotics active
against Chlamydia trachomatis and
Enterobacteriaceae in young sexually
active men; in older men without sexual
risk factors only Enterobacteriaceae have
to be considered.
If gonorrhoeal infection is likely give single Strong
dose ceftriaxone 500 mg intramuscularly in
addition to a course of an antibiotic active
against Chlamydia trachomatis.
Adjust antibiotic agent when pathogen Weak
has been identified and adjust duration
according to clinical response.
Follow national policies on reporting and Strong
tracing/treatment of contacts for sexually
transmitted infections.
Fournier’s Gangrene
Fournier’s gangrene is an aggressive and frequently fatal
polymicrobial soft tissue infection of the perineum, peri-anal
region, and external genitalia. It is an anatomical sub-category
of necrotising fasciitis with which it shares a common
aetiology and management pathway.

Recommendations for the disease Strength rating
management of Fournier’s Gangrene
Start treatment for Fournier’s gangrene Strong
with broad-spectrum antibiotics on
presentation, with subsequent refinement
according to culture and clinical response
Commence repeated surgical debridement Strong
for Fournier’s gangrene within 24 hours of
presentation.
Do not use adjunctive treatments for Weak
Fournier’s gangrene except in the context
of clinical trials.

Fournier’s Gangrene of mixed microbiological aetiology
Antimicrobial Dosage
Piperacillin-tazobactam plus 3.37 g every 6-8 h IV
vancomycin 15 mg/kg every 12 h
Imipenem-cilastatin 1 g every 6-8 h IV
Meropenem 1 g every 8 h IV
Ertapenem 1 g once daily
Cefotaxime plus 2 g every 6 h IV
metronidazole or 500 mg every 6 h IV
clindamycin 600-900 mg every 8 h IV
IV = intravenous
Detection of bacteriuria prior to urological procedures

Identifying bacteriuria prior to diagnostic and therapeutic
procedures aims to reduce the risk of infectious complications
by controlling any pre-operative detected bacteriuria and
to optimise antimicrobial coverage in conjunction with the
procedure.

Recommendation for the detection of Strength rating
bacteriuria prior to urological procedures
Use laboratory urine culture to detect Weak
bacteriuria in patients prior to undergoing
urological interventions breaching the
mucosa.
Peri-Procedural Antibiotic Prophylaxis

The available evidence enabled the panel to make
recommendations concerning urodynamics, cystoscopy,
stone procedures (extracorporeal shockwave lithotripsy,
ureteroscopy and percutaneous neprolithotomy), and
transurethral resection of the prostate and blabber. For
nephrectomy and prostatectomy the scientific evidence was
too weak to allow the panel to make recommendations either
for or against antibiotic prophylaxis.
Recommendations for peri-procedural Strength rating

antibiotic prophylaxis
Do not use antibiotic prophylaxis to reduce Strong
the rate of symptomatic urinary infection
following:
• urodynamics;
• cystoscopy;
• extracorporeal shockwave lithotripsy.
Use antibiotic prophylaxis to reduce the Weak
rate of symptomatic urinary infection
following ureteroscopy.
Use single dose antibiotic prophylaxis to Strong
reduce the rate of clinical urinary infection
following percutaneous nephrolithotomy.

Use antibiotic prophylaxis to reduce Strong
infectious complications in men
undergoing transurethral resection of the
prostate.
Use antibiotic prophylaxis to reduce Weak
infectious complications in high-risk
patients undergoing transurethral resection
of the bladder.
Prostate biopsy
Infection is the most clinically significant harm experienced
by men following prostate biopsy. Infection generally occurs
by implantation of rectal commensal organisms into the
prostate, urethra or bloodstream during needle insertion.
Severity of infection will depend on bacterial inoculum,
virulence and status of host defence.
Recommendations for non-antimicrobial Strength rating

intervention and antimicrobial prophylaxis
prior to prostate biopsy
Use rectal cleansing with povidone-iodine Strong
in men prior to transrectal prostate biopsy.
Use antimicrobial prophylaxis in men prior Strong
to transrectal prostate biopsy.


EAU GUIDELINES ON UROLITHIASIS
C. Türk (Chair), A. Petrik, A. Neisius, C. Seitz, A. Skolarikos,

K. Thomas
Guidelines Associates: J.F. Donaldson, T. Drake, N. Grivas,
Y. Ruhayel
Aetiology and classification

Urinary stones can be classified according to the following
aspects: aetiology of stone formation, stone composition
(mineralogy), stone size, stone location and X-ray characteris-
tics of the stone. The recurrence risk is basically determined
by the disease or disorder causing the stone formation.
Risk groups for stone formation

The risk status of stone formers is of particular interest
because it defines the probability of recurrence or regrowth,
and is imperative for pharmacological treatment (Table 1).
Table 1: High-risk stone formers
General factors
Early onset of urolithiasis (especially children and teenagers)
Familial stone formation
Brushite-containing stones (CaHPO4.2H2O)
Uric acid and urate-containing stones
Infection stones
Solitary kidney (the kidney itself does not particularly
increase risk of stone formation, but prevention of stone
recurrence is of more importance)
Urolithiasis 273
Diseases associated with stone formation
Hyperparathyroidism
Metabolic syndrome
Nephrocalcinosis
Polycystic kidney disease (PKD)
Gastrointestinal diseases (i.e., jejuno-ileal bypass, intestinal
resection, Crohn’s disease, malabsorptive conditions, enteric
hyperoxaluria after urinary diversion) and bariatric surgery
Sarcoidosis
Spinal cord injury, neurogenic bladder
Genetically determined stone formation
Cystinuria (type A, B and AB)
Primary hyperoxaluria (PH)
Renal tubular acidosis (RTA) type I
2,8-Dihydroxyadeninuria
Xanthinuria
Lesch-Nyhan syndrome
Cystic fibrosis
Drug-induced stone formation
Anatomical abnormalities associated with stone formation
Medullary sponge kidney (tubular ectasia)
Ureteropelvic junction (UPJ) obstruction
Calyceal diverticulum, calyceal cyst
Ureteral stricture
Vesico-uretero-renal reflux
Horseshoe kidney
Ureterocele
Environmental factors
Chronic lead exposure
274 Urolithiasis
Diagnostic imaging
Standard evaluation of a patient includes taking a detailed
medical history and physical examination. The clinical
diagnosis should be supported by appropriate imaging.
Recommendation Strength
rating
With fever or solitary kidney, and when diagnosis Strong
is doubtful, immediate imaging is indicated.
Ultrasound (US) should be used as the primary diagnostic

imaging tool, although pain relief, or any other emergency
measures, should not be delayed by imaging assessments.
Kidney-ureter-bladder (KUB) urography should not be
performed if non-contrast-enhanced computed tomography
(NCCT) is considered, but KUB urography can differentiate
between radiolucent and radiopaque stones and be used for
comparison during follow up.
Recommendation for radiologic examinations Strength

of patients with acute flank pain/suspected rating
ureteral stones
Following initial ultrasound assessment, use Strong
non-contrast-enhanced computed tomography
to confirm stone diagnosis in patients with acute
flank pain.
Urolithiasis 275
Recommendation for radiologic examination of Strength
patients with renal stones rating
Perform a contrast study if stone removal is Strong
planned and the anatomy of the renal collecting
system needs to be assessed.
Diagnostics: Metabolism-related
Each emergency patient with urolithiasis needs a succinct
biochemical work-up of urine and blood; no difference is made
between high- and low-risk patients.
Recommendations: basic laboratory analysis - Strength

emergency stone patient rating
Urine
Dipstick test of spot urine sample Strong
• red cells;
• white cells;
• nitrite;
• approximate urine pH;
• urine microscopy and/or culture.
Blood
Serum blood sample Strong
• creatinine;
• uric acid;
• (ionised) calcium;
• sodium;
• potassium;
• blood cell count;
• C-reactive protein.
Perform a coagulation test (partial thrombo Strong
plastin time and international normalised ratio) if
intervention is likely or planned.
276 Urolithiasis
Examination of sodium, potassium, C-reactive protein (CRP),
and blood coagulation time can be omitted if no intervention
is planned in non-emergency stone patients. Patients at high
risk for stone recurrences should undergo a more specific
analytical programme (see section on Metabolic Evaluation
below).
Recommendations related to stone analysis Strength

rating
Perform stone analysis in first-time stone formers Strong
using a validated procedure (X-ray diffraction or
infrared spectroscopy).
Repeat stone analysis in patients: Strong
• presenting with recurrent stones despite drug
therapy;
• with early recurrence after complete stone
clearance;
• with late recurrence after a long stone-free
period because stone composition may
change.
Diagnosis for special groups/conditions

Pregnancy
Recommendations Strength
rating
Use ultrasound as the preferred method of Strong
imaging in pregnant women.
In pregnant women, use magnetic resonance Strong
imaging as a second-line imaging modality.
In pregnant women, use low-dose Strong
computed tomography as a last-line option.
Urolithiasis 277
Children
rating
In all children, complete a metabolic evaluation Strong
based on stone analysis.
Collect stone material for analysis to classify the Strong
stone type.
Perform ultrasound (US) as first-line imaging Strong
modality in children when a stone is suspected; it
should include the kidney, fluid-filled bladder and
the ureter.
Perform a kidney-ureter-bladder radiography Strong
(or low-dose non-contrast-enhanced computed
tomography) if US will not provide the required
information.
In children, the most common non-metabolic disorders

facilitating stone formation are vesicoureteral reflux,
UPJ obstruction, neurogenic bladder, and other voiding
difficulties.
The radiation dose for intravenous urography (IVU) is

comparable to that for voiding cystourethrography, but the
need for contrast medium injection is a major drawback.
278 Urolithiasis
Disease Management
Acute treatment of a patient with renal colic
Pain relief is the first therapeutic step in patients with an
acute stone episode.
Recommendations for pain relief during and Strength

prevention of recurrent renal colic rating
Offer a non-steroidal anti-inflammatory as the Strong
first drug of choice. e.g. metamizol (dipyrone);
alternatively, paracetamol or, depending on
cardio-vascular risk factors, diclofenac*,
indomethacin or ibuprofen**.
Offer hydromorphine, pentazocine or tramadol as Weak
a second choice.
Offer renal decompression or ureteroscopic stone Strong
removal in case of analgesic refractory colic pain.
*A ffects glomerular filtration rate in patients with reduced
renal function.
** R ecommended to counteract recurrent pain after renal
colic (see extended document).
Administration of daily α-blockers seems to reduce colic

episodes, although controversy remains in the published
literature.
If analgesia cannot be achieved medically, drainage, using

stenting or percutaneous nephrostomy, or stone removal,
should be performed.
Urolithiasis 279
Management of sepsis and anuria in the obstructed kidney
The obstructed, infected, kidney is a urological emergency.
rating
Urgently decompress the collecting system in Strong
case of sepsis with obstructing stones, using
percutaneous drainage or ureteral stenting.
Delay definitive treatment of the stone until Strong
sepsis is resolved.
In exceptional cases, with severe sepsis and/or the formation of

abscesses, an emergency nephrectomy may become necessary.
Recommendations - Further measures Strength

rating
Collect urine for antibiogram test following Strong
decompression.
Start antibiotics immediately (+ intensive care if Strong
necessary).
Re-evaluate antibiotic treatment regimen Strong
following antibiogram findings.
Medical expulsive therapy (MET)

Medical expulsive therapy should only be used in informed
patients. Treatment should be discontinued if complications
develop (infection, refractory pain, deterioration of kidney
function).
Medical expulsive therapy, using α-blockers, seems to be

efficacious treating patients with ureteric stones that are
amenable to conservative management. Patients benefitting
most might be those with larger (distal) stones.
280 Urolithiasis
There is no or insufficient evidence to support the use of
Phosphodiesterase type 5 inhibitor (PDE-5i) or corticosteroids
in combination with α-blockers as a standard adjunct to
active stone removal.
Recommendation for medical expulsive therapy Strength

(MET) rating
Offer α-blockers as medical expulsive therapy as Strong
one of the treatment options for (distal) ureteral
stones > 5 mm.
Chemolytic dissolution of stones

Oral chemolysis of stones or their fragments can be useful
in uric acid stones. It is based on alkalinisation of urine by
application of alkaline citrate or sodium bicarbonate. The pH
should be adjusted to 7.0-7.2.
Recommendations - Oral chemolysis Strength

rating
Inform the patient how to monitor urine-pH by Strong
dipstick and to modify the dosage of alkalising
medication according to urine pH, as changes
in urine pH are a direct consequence of such
medication.
Carefully monitor patients during/after oral Strong
chemolysis for uric acid stones.
Combine oral chemolysis with Tamsulosin in case Weak
of (larger) ureteral stones (if active intervention is
not indicated).
Percutaneous irrigation chemolysis is rarely used any more.
Urolithiasis 281
Shockwave lithotripsy (SWL)
The success rate for SWL will depend on the efficacy of the
lithotripter and on:
• size, location (ureteral, pelvic or calyceal), and composition
(hardness) of the stones;
• patient’s habitus;
• performance of SWL.
Contraindications of SWL
Contraindications are few, but include:
• pregnancy;
• bleeding diatheses; which should be compensated for at
least 24 hours before and 48 hours after treatment;
• untreated urinary tract infections (UTIs);
• severe skeletal malformations and severe obesity, which
prevent targeting of the stone;
• arterial aneurysm in the vicinity of the stone;
• anatomical obstruction distal to the stone.
Best clinical practice (best performance) in SWL

Stenting prior to SWL
Routine use of internal stents before SWL does not improve
stone-free rates, nor lowers the number of auxiliary treat-
ments. It may, however, reduce formation of steinstrasse.
Pacemaker
Patients with a pacemaker can be treated with SWL. Patients
with implanted cardioverter defibrillators must be managed
with special care (firing mode temporarily reprogrammed
during SWL treatment). However, this might not be necessary
with new-generation lithotripters.
282 Urolithiasis
Shock waves, energy setting and repeat treatment sessions
• The number of shock waves that can be delivered at each
session depends on the type of lithotripter and shockwave
power.
• Starting SWL on a lower energy setting with step-wise
power ramping prevents renal injury.
• Optimal shock wave frequency is 1.0 to 1.5 Hz.
• Clinical experience has shown that repeat sessions are
feasible (within one day for ureteral stones).
Procedural control
Recommendations - Procedural control Strength

rating
Ensure correct use of the coupling agent as this is Strong
crucial for effective shock wave transportation.
Maintain careful fluoroscopic and/or Strong
ultrasonographic monitoring during shock wave
lithotripsy.
Use proper analgesia as it improves treatment Strong
results by limiting pain and excessive respiratory
excursions.
Antibiotic prophylaxis
No standard prophylaxis prior to SWL is recommended.
rating
In the case of infected stones or bacteriuria, Strong
prescribe antibiotics prior to shockwave
lithotripsy.
Urolithiasis 283
Ureterorenoscopy (URS) (retrograde and antegrade, RIRS)
Apart from general problems, for example, with general
anaesthesia or untreated UTIs, URS can be performed in all
patients without any specific contraindications.
If ureteral access is not possible, insertion of a JJ stent
followed by URS after several days is an alternative. During
URS, placement of a safety wire is recommended, even though
some groups have demonstrated that URS can be performed
without it.
Ureteral access sheaths allow easy, multiple, access to the
upper urinary tract; however, its insertion may lead to ureteral
damage.
rating
Use holmium: yttrium-aluminium-garnet (Ho:YAG) Strong
laser lithotripsy for (flexible) ureterorenoscopy.
Perform stone extraction only under direct Strong
endoscopic visualisation of the stone.
Do not insert a stent in uncomplicated cases. Strong
Pre-stenting facilitates ureterorenoscopy (URS) Strong
and improves outcomes of URS (in particular for
renal stones).
Offer MET for patients suffering from stent- Strong
related symptoms and after Ho:YAG laser
lithotripsy for the passage of fragments.
Percutaneous nephrolithotomy (PNL)

Patients with bleeding diathesis or receiving anticoagulant
therapy must be monitored carefully pre- and post-operatively.
Anticoagulant therapy must be discontinued before PNL
contraindications, which include:
• untreated UTI;
• tumour in the presumptive access tract area;
284 Urolithiasis
• potential malignant kidney tumour;
• pregnancy.
Best clinical practice

Both prone and supine positions are equally safe.
Percutaneous nephrolithotomy performed with small
instruments tended to be associated with significantly
lower blood loss, but the duration of procedure tended to
be significantly longer.
rating
Perform pre-procedural imaging, including Strong
contrast medium where possible or retrograde
study when starting the procedure, to assess
stone comprehensiveness and anatomy of the
collecting system to ensure safe access to the
renal stone.
In uncomplicated cases, perform a tubeless Strong
(without nephrostomy tube) or totally tubeless
(without nephrostomy tube and ureteral stent)
percutaneous nephrolithotomy procedure.
Urolithiasis 285
Stone Removal
rating
Obtain a urine culture or perform urinary Strong
microscopy before any treatment is planned.
Exclude or treat urinary tract infection prior to Strong
stone removal.
Offer peri-operative antibiotic prophylaxis to all Strong
patients undergoing endourological treatment.
Offer active surveillance to patients at high risk Weak
for thrombotic complications in the presence of
an asymptomatic calyceal stone.
Decide on temporary discontinuation, or bridging Strong
of antithrombotic therapy in high-risk patients, in
consultation with the internist.
Retrograde (flexible) ureterorenoscopy Is Strong
the preferred intervention if stone removal is
essential and antithrombotic therapy cannot
be discontinued, since it is associated with less
morbidity.
Radiolucent uric acid stones can be dissolved by oral

chemolysis.
Ureteral stones
Observation of ureteral stones is feasible in informed patients
who develop no complications (infection, refractory pain,
deterioration of kidney function).
286 Urolithiasis
rating
In patients with newly diagnosed small* ureteral Strong
stones, if active stone removal is not indicated,
observe patient initially along with periodic
evaluation.
Offer α-blockers as medical expulsive therapy as Strong
one of the treatment options for (distal)ureteral
stones ≥ 5 mm.
Inform patients that ureterorenoscopy (URS) has Strong
a better chance of achieving stone-free status
with a single procedure.
Inform patients that URS has higher complication Strong
rates when compared to shock wave lithotripsy.
In cases of severe obesity use URS as first-line Strong
therapy for ureteral (and renal) stones.
*see stratification data (J Urol, 2007. 178: 2418).
Indication for active stone removal and selection of

procedure
Ureter:
• stones with a low likelihood of spontaneous passage;
• persistent pain despite adequate pain medication;
• persistent obstruction;
• renal insufficiency (renal failure, bilateral obstruction,
single kidney).
The suspected stone composition might influence the choice

of treatment modality.
Urolithiasis 287
Figure 1: Treatment algorithm for ureteral stones (If active
stone removal is indicated) (Strength rating: Strong)
Proximal Ureteral Stone
1. URS (ante- or retrogade)

> 10 mm
2. SWL
< 10 mm SWL or URS
Distal Ureteral Stone
1. URS
> 10 mm
2. SWL
< 10 mm SWL or URS
SWL = shock wave lithotripsy; URS = ureterorenoscopy.
rating
Use percutaneous antegrade removal of ureteral Strong
stones as an alternative when shockwave
lithotripsy is not indicated or has failed, and
when the upper urinary tract is not amenable to
retrograde ureterorenoscopy.
288 Urolithiasis
Renal stones
It is still debatable whether renal stones should be treated,
or whether annual follow-up is sufficient for asymptomatic
calyceal stones that have remained stable for six months.
rating
Follow-up periodically in cases where renal Strong
stones are not treated (initially after six months
and then yearly, evaluating symptoms and stone
status [either by ultrasound, kidney-ureter-
bladder radiography or computed tomography]).
Offer active treatment for renal stones in case of Weak
stone growth, de novo obstruction, associated
infection, and acute and/or chronic pain.
Assess comorbidity, stone composition and Weak
patient preference when making treatment
decisions.
Offer shock wave lithotripsy (SWL) and Strong
endourology (percutaneous nephrolithotomy
[PNL], retrograde renal surgery [RIRS]) as
treatment options for stones < 2 cm within the
renal pelvis and upper or middle calices.
Perform PNL as first-line treatment of larger Strong
stones > 2 cm.
In case PNL is not an option, treat larger stones Strong
(> 2 cm) with flexible ureterorenoscopy or SWL.
However, in such instances there is a higher risk
that a follow-up procedure and placement of a
ureteral stent may be needed.
Urolithiasis 289
For the lower pole, perform PNL or RIRS, even for Strong
stones > 1 cm, as the efficacy of SWL is limited
(depending on favourable and unfavourable
factors for SWL).
Indication for active stone removal and selection of

procedure
Kidney:
• stone growth;
• stones in high-risk patients for stone formation;
• obstruction caused by stones;
• infection;
• symptomatic stones (e.g. pain, haematuria);
• stones > 15 mm;
• stones < 15 mm if observation is not the option of choice;
• patient preference;
• comorbidity;
• social situation of the patient (e.g., profession or travelling);
• choice of treatment.
The suspected stone composition might influence the choice

of treatment modality.
290 Urolithiasis
Figure 2: Treatment algorithm for renal stones (if active
treatment is indicated). (Strength rating: Strong)
Kidney stone
(all but lower pole stone 10-20 mm)
1. PNL
> 20 mm
2. RIRS or SWL
10-20 mm SWL or Endourology*
1. SWL or RIRS
< 10 mm
2. PNL
Lower pole stone

> 20 mm and < 10 mm: as above
No SWL or Endourology*
Unfavourable
10-20 mm
factors for SWL
1. Endourology*
Yes 2. SWL
*T
he term ‘Endourology’ encompasses all PNL and URS
interventions.
PNL = percutaneous nephrolithotomy; RIRS = retrograde renal
surgery; SWL = shockwave lithotripsy; URS = ureterorenoscopy.
Urolithiasis 291
rating
Use flexible ureterorenoscopy in cases where Strong
percutaneous nephrolithotomy or shockwave
lithotripsy are not an option (even for stones
> 2 cm). However, in this case there is a higher
risk that a follow-up procedure and placement of
a ureteral stent may be needed. In complex stone
cases, use open or laparoscopic approaches as
possible alternatives.
Open and laparoscopic surgery
rating
Offer laparoscopic or open surgical stone Strong
removal in rare cases in which shockwave
lithotripsy (SWL), (flexible) ureterorenoscopy and
percutaneous nephrolithotomy fail, or are unlikely
to be successful.
Perform surgery laparoscopically before Strong
proceeding to open surgery.
For ureterolithotomy, perform laparoscopy Strong
for large impacted stones when endoscopic
lithotripsy or SWL has failed, or is contraindicated.
Steinstrasse
The major factor in steinstrasse formation is stone size.
Medical expulsion therapy increases the stone expulsion rate
of steinstrasse. When spontaneous passage is unlikely, further
treatment of steinstrasse is indicated.
292 Urolithiasis
rating
Treat steinstrasse associated with urinary tract Weak
infection/fever preferably with percutaneous
nephrostomy.
Treat steinstrasse when large stone fragments Weak
are present with shockwave lithotripsy or
ureterorenoscopy.
Management of patients with residual stones

Following initial treatment with SWL, URS or PNL residual
fragments may remain and require additional intervention. The
indications for active removal of residual stones and selection
of the procedure are based on the same criteria as for primary
stone treatment. For well-disintegrated stone material in the
lower calix, inversion therapy with simultaneous mechanical
percussion manoeuvre under enforced diuresis may facilitate
stone clearance.
Recommendation in case of residual fragments Strength

rating
Perform imaging after shockwave lithotripsy, Strong
ureterorenoscopy or percutaneous nephrostomy
to determine presence of residual fragments.
Management of urinary stones and related problems during

pregnancy
rating
Treat all uncomplicated cases of urolithiasis in Strong
pregnancy conservatively (except those that have
clinical indications for intervention).
Urolithiasis 293
If intervention becomes necessary, placement of a ureteral
stent or a percutaneous nephrostomy tube are readily
available primary options. Ureteroscopy is a reasonable
alternative to avoid long-term stenting/drainage. There is a
higher tendency for stent encrustation during pregnancy.
Management of stones in patients with urinary diversion

Patients with urinary diversion are at high risk for stone
formation in the renal collecting system and ureter or in the
conduit or continent reservoir.
rating
Perform percutaneous lithotomy to remove large Strong
renal stones in patients with urinary diversion,
as well as for ureteral stones that cannot be
accessed via a retrograde approach or that are
not amenable to shockwave lithotripsy.
Management of stones in patients with neurogenic bladder

Patients with neurogenic bladder are more prone to develop-
ment of urinary calculi.
In myelomeningocoele patients, latex allergy is common so
that appropriate measures need to be taken regardless of the
treatment.
Management of stones in transplanted kidneys

Transplanted patients are at additional risk due to their
dependency on a solitary kidney, immunosuppression therapy
and possible metabolic impairments. Conservative treatment
for small asymptomatic stones is only possible under close
surveillance and in absolutely compliant patients.
Stones causing urinary stasis/obstruction require
immediate intervention or drainage of the transplanted kidney.
294 Urolithiasis
rating
Perform ultrasound or non-contrast-enhanced Strong
computed tomography to rule out calculi in
patients with transplanted kidneys, unexplained
fever, or unexplained failure to thrive (particularly
in children).
Offer patients with transplanted kidneys, Weak
any of the contemporary management
options, including shockwave therapy,
flexible ureterorenoscopy, and percutaneous
nephrolithotomy.
Special problems in stone removal
Calyceal • S hockwave lithotripsy (SWL),

diverticulum percutaneous nephrolithotomy (PNL)
stones (if possible) or retrograde renal surgery
(RIRS).
• Can also be removed using laparoscopic
retroperitoneal surgery.
• Patients may become asymptomatic
due to stone disintegration (SWL),
whilst well-disintegrated stone material
remains in the original position due to a
narrow calyceal neck.
Horseshoe • Can be treated in line with the options
kidneys described above.
• Passage of fragments after SWL might
be poor.
• Acceptable stone-free rates (SFRs)
can be achieved with flexible
ureterorenoscopy (URS).
Urolithiasis 295
Stones in • S WL, RIRS, PNL or laparoscopic surgery.
pelvic kidneys • In obese patients, the options are RIRS,
PNL or open surgery.
Patients with • When outflow abnormality requires
obstruction correction, stones can be removed
of the by PNL together with percutaneous
ureteropelvic endopyelotomy or open/laparoscopic
junction reconstructive surgery.
• Ureterorenoscopy together with
endopyelotomy with holmium-
yttrium-aluminium-garnet laser.
• Incision with an Acucise® balloon
catheter might be considered, provided
the stones can be prevented from falling
into the pyeloureteral incision.
• Open surgery with correction of the
UPJ obstruction (pyloplasty) and stone
removal is a feasible option.
Management of urolithiasis in children

In children, the indication for SWL and for PNL is similar to
those in adults. Compared to adults, children pass fragments
more rapidly after SWL. For endourological procedures, the
smaller organs in children must be considered when selecting
instruments for PNL or URS.
Children with renal stones of a diameter up to 20 mm
(~300 mm2) are ideal candidates for SWL.
296 Urolithiasis
rating
Offer children with ureteral stones shockwave Strong
lithotripsy (SWL) as first-line but consider uretero
renoscopy if SWL is not possible and in case of
larger distal ureteric stones.
Offer children with renal stones with a diameter Strong
of up to 20 mm (~300 mm2) SWL.
Offer children with renal pelvic or calyceal Strong
stones with a diameter > 20 mm(~300 mm2)
percutaneous nephrolithotomy.
Metabolic evaluation and recurrence prevention

After stone passage, every patient should be assigned to
a low- or high-risk group for stone formation. For correct
classification, two analyses are mandatory:
• reliable stone analysis by infrared spectroscopy or X-ray
diffraction;
• basic analysis.
Only high-risk stone formers require specific metabolic

evaluation. Stone type is the deciding factor for further
diagnostic tests. For both groups, general preventive
measures apply:
General preventive measures

Fluid intake (drinking Fluid amount: 2.5-3.0 L/day
advice) Circadian drinking
Neutral pH beverages
Diuresis: 2.0-2.5 L/day
Specific weight of urine: < 1010 L/day
Urolithiasis 297
Nutritional advice for Rich in vegetables and fibre
a balanced diet Normal calcium content: 1-1.2 g/day
Limited NaCl content: 4-5 g/day
Limited animal protein content:
0.8-1.0 g/kg/day
Avoid excessive consumption of
vitamin supplements
Lifestyle advice to Body mass index (BMI): retain a
normalise general normal BMI level
risk factors Adequate physical activity
Balancing of excessive fluid loss
Caution: The protein need is age-group dependent; therefore,
protein restriction in childhood should be handled carefully.
Calcium oxalate stones

Hyperparathyroidism is excluded by blood analysis.
Recommendations for pharmacological treatment of

patients with specific abnormalities in urine composition
(based on 24-hour urine samples)
Urinary risk factor Suggested treatment Strength
rating
Hypercalcuria Thiazide + potassium Strong
citrate
Hyperoxaluria Oxalate restriction Weak
Enteric hyperoxaluria Potassium citrate Weak
Calcium supplement Weak
Diet reduced in fat and Weak
oxalate
Hypocitraturia Potassium citrate Strong
Hypocitraturia Sodium bicarbonate if Strong
intolerant to potassium
citrate
298 Urolithiasis
Hyperuricosuria Allopurinol Strong
Febuxostat Strong
High sodium Restricted intake of salt Strong
excretion
Small urine volume Increased fluid intake Strong
Urea level indicating Avoid excessive intake of Strong
a high intake of animal protein
animal protein
Urolithiasis 299
1
2
300 Urolithiasis
Calcium oxalate stone
therapy alone.
Basic evaluation
24 h urine collection
oxalate stones
5 Febuxostat 80 mg/day.
Hypercalcuria Hypocitraturia Hyperoxaluria Hyperuricosuria Hypomagnesuria
tid = three times/day (24h).

Hyperuricosuria
Male < 1.7 mmol/d > 0.5 mmol/d > 1 mmol/d and
5-8 mmol/d2 8 mmol/d > 4 mmol/d Hyperuricaemia < 3 mmol/d
Female < 1.9 mmol/d (Enteric) (Primary)
> 380μmol/L
Be aware of excess calcium excretion.

alkaline
citrate
alkaline hydrochlorothiazide 9-12 g/d
citrate initially 25 mg/d calcium Pyridoxine OR alkaline citrate
9-12 g/d up to 50 mg/d alkaline > 1000 mg/d1 initial 5 sodium 9-12 g/d
OR chlorthalidone and mg/kg/d PLUS magnesium
citrate bicarbonate
sodium 25 mg/d magnesium up to allopurinol 200-400 mg/d3
9-12 g/d 1.5 g tid2
bicarbonate indapamide 200-400 mg/d 20 mg/kg/d PLUS/OR 100-300 mg/d4,5
1.5 g tid2,4 2.5 mg/d allopurinol
100 mg/d
4 There is no evidence that combination therapy (thiazide
+ citrate) or (thiazide + allopurinol) is superior to thiazide

Figure 3: Diagnostic and therapeutic algorithm for calcium
3 No magnesium therapy for patients with renal insufficiency.

Figure 4: Diagnostic and therapeutic algorithm for calcium
phosphate stones
Calcium phosphate
stones
Carbonate
apatite Brushite stones
stones
Basis evaluation Basis evaluation
Urinary pH Elevated calcium

Hypercalciuria Exclude HPT Exclude RTA
> 6.5-6.8 exclude HPT
hydrochlorothiazide Hypercalciuria
initially 25 mg/d Exclude RTA Exclude UTI > 8 mmol/d
up to 50 mg/d
Adjust urinary pH hydrochlorothiazide

between 5.8 and 6.2 initially 25 mg/d
with L-methionine up to 50 mg/d
200-500 mg chlorthalidone 25 mg/d
three times daily indapamide 2.5 mg/d
HPT = hyperparathyroidism; RTA = renal tubular acidosis;

UTI = urinary tract infection.
rating
Prescribe thiazide in case of hypercalciuria. Strong
Advise patients to acidify their urine in case of Weak
high urine pH.
Hyperparathyroidism
Elevated levels of ionized calcium in serum (or total calcium
and albumin) require assessment of intact parathyroid hor-
mone to confirm or exclude suspected hyperparathyroidism
(HPT). Primary HPT can only be cured by surgery.
Urolithiasis 301
Figure 5: Diagnostic and therapeutic algorithm for uric acid
and urate-containing stones
Uric acid- and urate-

containing stones
Ammonium
Urate acid stone
urate stones
Basic evaluation Basic evaluation
“Uric acid arrest” Urine

Hyperuricosuria
Urine pH < 6 pH > 6.5
alcaline citrate > 4.0 mmol/d UTI L-methionine

> 4.0 mmol/d
9-12 g/d1 200-500 mg tid
and
OR Target urine-pH
Hyperuricemia
sodium 5.8-6.2
> 380 μmol
bicarbonate Allopurinol
1.5 g tid2 100 mg/d Antibiotics
Allopurinol Correction
100-300 mg/d of factors
Dose depends
predisposing
on targeted
ammonium
urine pH
urate stone
formation4
Prevention Chemolysis
urine pH 6.2-6.8 urine pH 6.5-7.23
UTI = urinary tract infection.

1 d: day.
2 tid: three times a day.
3 A higher pH may lead to calcium phosphate stone formation.
4 In patients with high uric acid excretion, allopurinol may be
helpful.
302 Urolithiasis
Figure 6: Metabolic management of cystine stones.
Cystine stones
Basic evaluation
Appropriate hydration with

> 3.5 L/d in adults and
1.5 L/m2 body surface in
children
AND
adjust urine pH
between 7.5 and 8.5
with
alkaline citrates or
sodium bicarbonate
Cystine excretion Cystine excretion

< 3 mmol/d > 3 mmol/d
Possible add. treatment Additional treatment with

with tiopronin tiopronin 250 mg/d up to
(depending on recurrence) 2,000 mg/d max. dos.
Urolithiasis 303
Struvite/infection stones
Recommendations for therapeutic measures of Strength

infection stones rating
Surgically remove the stone material as Strong
completely as possible.
Prescribe antibiotics in case of persistent Strong
bacteriuria.
Prescribe ammonium chloride, 1 g, two or three Weak
times daily to ensure urinary acidification.
Prescribe methionine, 200-500 mg, one to three Weak
times daily, as an alternative, to ensure urinary
acidification.
2,8-Dihydroyadenine stones and xanthine stones

Both stone types are rare. In principle, diagnosis and specific
prevention is similar to that of uric acid stones.
Drug stones
Drug stones are induced by pharmacological treatment. Two
types exist:
• stones formed by crystallised compounds of the drug;
• stones formed due to unfavourable changes in urine
composition under drug therapy.
Treatment includes general preventive measures and the
avoidance of the respective drugs.
304 Urolithiasis
Investigating a patient with stones of unknown composition
Investigation Rationale for investigation

Medical history • Stone history (former stone events,
family history)
• Dietary habits
• Medication chart
Diagnostic • Ultrasound in the case of a suspected
imaging stone
• Unenhanced helical computed
tomography
• Determination of Hounsfield units
provides information on the possible
stone composition
Blood analysis • Creatinine
• Calcium (ionised calcium or total
calcium + albumin)
• Uric acid
Urinalysis • Urine pH profile (measurement after
each voiding, minimum four times daily)
• Dipstick test: leukocytes, erythrocytes,
nitrite, protein, urine pH, specific weight
• Urine culture
• Microscopy of urinary sediment
(morning urine)
• Cyanide nitroprusside test (cysteine
exclusion)
Further examinations depend on the results of the

investigations listed above.

EAU Guidelines (978-94-92671-01-1) available to all members of the
Urolithiasis 305
EAU GUIDELINES ON
PAEDIATRIC UROLOGY
C. Radmayr (Chair), G. Bogaert, H.S. Dogan, R. Kočvara,

J.M. Nijman (Vice-chair), R. Stein, S. Tekgul
Guidelines Associates: L.A ‘t Hoen, J. Quaedackers, M.S. Silay,
S. Undre
Introduction
Due to the scope of the extended Guidelines on Paediatric
Urology, no attempt has been made to include all topics,
but rather to provide a selection based on practical
considerations.
PHIMOSIS
Background
At the end of the first year of life, retraction of the foreskin
behind the glandular sulcus is possible in 50% of boys. The
phimosis is either primary (physiological), with no sign of
scarring, or secondary (pathological), resulting from scarring
due to conditions such as balanitis xeroticaobliterans.
Phimosis must be distinguished from normal agglutination

of the foreskin to the glans, which is a physiological
phenomenon. If the tip remains narrow and glandular
adhesions are separated, then the space is filled with urine
during voiding, causing the foreskin to balloon outward.
Treatment
Conservative treatment
Administration of a corticoid ointment or cream is an option
for primary phimosis with a success rate of > 90%, but with a
306 Paediatric Urology

recurrence rate of 17%. Agglutination of the foreskin does not
respond to steroid treatment.
Circumcision: indication and contraindication

Childhood circumcision should not be recommended without
a medical reason. An absolute indication for circumcision is
secondary phimosis. Contraindications for circumcision are
acute local infection and congenital anomalies of the penis,
particularly hypospadias or buried penis, as the foreskin may
be required for a reconstructive procedure.
Plastic circumcision (dorsal incision, partial circumcision)
carries the potential for recurrence of phimosis. Associated
frenulum breve is corrected by frenulotomy. Meatoplasty is
added if necessary.
Paraphimosis
It is characterised by retracted foreskin with the constrictive
ring localised at the level of the sulcus. A dorsal incision of the
constrictive ring may be required, or circumcision is carried
out immediately or in a second session.
UNDESCENDED TESTES
Background
Cryptorchidism or undescended testis is one of the most
common congenital malformations of male neonates. In
newborn cases with non-palpable or undescended testes on
both sides and any sign of disorders of sex development (DSD)
like concomitant hypospadias, urgent endocrinological and
genetic evaluation is required.
Classification
The term cryptorchidism is most often used synonymously
for undescended testes. The most useful classification of
undescended testes is into palpable and non-palpable testes,
and clinical management is decided by the location and
Paediatric Urology 307

presence of the testes. Approximately 80% of all undescended
testes are palpable.
Palpable testes include true undescended testes and
ectopic testes. Non-palpable testes include intra-abdominal,
inguinal, absent, and sometimes also some ectopic testes.
Most importantly, the diagnosis of a palpable or non-
palpable testis needs to be confirmed once the child is under
general anaesthesia, as the first step of any surgical procedure
for undescended testes. See figure 1.
History taking and physical examination are key points in
evaluating boys with undescended testes. Localisation studies
using different imaging modalities are usually without any
additional benefit.
Management
Treatment should be started at the age of six months. After
that age, undescended testes rarely descend. Any kind of
treatment leading to a scrotally positioned testis should be
finished by twelve months, or eighteen months at the latest,
because histological examination of undescended testes at
that age has already revealed a progressive loss of germ and
Leydig cells. The early timing of treatment is also driven by
the final adult results on spermatogenesis and hormone
production, as well as on the risk of tumour development.
See figure 2.
Medical therapy for testicular descent

Unfortunately, most of the studies on hormonal treatment
have been of poor quality, with heterogeneous and mixed
patient populations, testis location, schedules and dosages
of hormonal administration. Additionally, long-term data are
almost completely lacking.

Hormonal therapy using human chorionic gonadotropin
or gonadotrophin-releasing hormone (GnRH) is based on
the h
ormonal dependence of testicular descent, but has a
maximum success rate of only 20%. In general, success rates
depend on testicular location. The higher the testis is located
prior to therapy, the lower the success rate. The Panel
consensus is that endocrine treatment to achieve testicular
descent is not recommended.
Medical therapy for fertility potential

Hormonal treatment may improve fertility indices and
therefore serve as an additional tool to orchidopexy. It is still
unknown whether this effect on testicular histology persists
into adulthood but it has been shown that men who were
treated in childhood with buserelin had better semen analyses
compared with men who had childhood orchidopexy alone or
placebo treatment.
Identification of specific subgroups of boys with
undescended testes who would benefit from such an
approach using hormones is difficult. The Panel consensus
recommends endocrine treatment with GnRH analogues for
boys with bilateral undescended testes to preserve the fertility
potential.
Surgical Treatment
If a testis has not concluded its descent at the age of six
months (corrected for gestational age), and since spontaneous
testicular descent is unlikely to occur after that age, surgery
should be performed within the subsequent year, at age
eighteen months, at the latest.
Palpable testes
Surgery for palpable testes includes orchidofunicolysis and
orchidopexy, either via an inguinal or scrotal approach.

Non-palpable testes
For non-palpable testes, surgery must clearly determine
whether a testis is present or not. If a testis is found, the
decision has to be made to remove it or bring it down to the
scrotum.
An important step in surgery is a thorough re-examination
once the boy is under general anaesthesia, since a previously
non-palpable testis might be identifiable and subsequently
change the surgical approach to standard inguinal
orchidopexy, as described above. Otherwise, the easiest and
most accurate way to locate an intra-abdominal testis is
diagnostic laparoscopy. Subsequent removal or orchidolysis
and orchidopexy can be carried out using the same approach
to achieve the therapeutic aims.
In case of a vanishing testis, the procedure is finished once
blind-ending spermatic vessels are clearly identified. If the
vessels enter the inguinal canal, one may find an atrophic
testis upon inguinal exploration or a healthy testis that needs
to undergo standard orchidopexy. A peeping testis can be
placed down in the scrotum laparoscopically or via an
inguinal incision. Placement of an intra-abdominal testis can
sometimes be a surgical challenge. Usually, testes lying > 2 cm
above the internal inguinal ring may not reach the scrotum
without division of the testicular vessels. Under such
circumstances, a Fowler–Stephens orchidopexy might be an
option.
Undescended testes and fertility

The association of undescended testes with compromised
fertility is extensively discussed in the literature and seems
to be a result of multiple factors, including germ cell loss,
impaired germ cell maturation, Leydig cell diminution, and
testicular fibrosis.

Although boys with one undescended testis have a lower
fertility rate, they have the same paternity rate as those with
bilateral descended testes. Boys with bilateral undescended
testes suffer both lower fertility and paternity rates.
Regarding preservation of fertility potential, early surgical
correction of undescended testes is highly recommended
before twelve months of age, and by eighteen months at the
latest.
Undescended testes and malignancy

Boys who are treated for an undescended testis have an
increased risk of developing testicular malignancy. Screening
and self-examination during and after puberty is therefore
recommended.
Pre-pubertal orchidopexy may reduce the risk of testicular
cancer and early surgical intervention is indicated in boys with
undescended testes.

The Panel do not recommend medical or Strong
surgical treatment for retractile testes but
recommend close follow-up on a yearly
basis until puberty.
Perform surgical orchidolysis and Strong
orchidopexy before the age of twelve
months, and by eighteen months at the
latest.
Evaluate male neonates with bilateral non- Strong
palpable testes for possible disorders of sex
development.
Perform a diagnostic laparoscopy to locate Strong
an intra-abdominal testicle.

Hormonal therapy in unilateral Weak
undescended testes is of no benefit for
future paternity.
Offer endocrine treatment in case of Weak
bilateral undescended testes.
Inform the patient/caregivers about the Weak
increased risk of a later malignancy with
an undescended testis in a post-pubertal
boy or older and discuss removal in case
of a contralateral normal testis in a scrotal
position.
Figure 1: Classification of undescended testes
Undescended testis
Palpable Non-palpable
Intra-
Inguinal Inguinal Ectopic Absent
abdominal
Ectopic
Agenesis
Retractile
Vanishing
testis

Figure 2: Algorithm for the management of unilateral
non-palpable undescended testis
Unilateral non-palpable
testis
Re-exam under
anaesthesia
Still
Palpable
non-palpable
Inguinal
Diagnostic exploration Standard
laparoscopy with possible orchidopexy
laparoscopy
Blind ending Spermatic

Testis close to Testis too high
spermatic vessels enter
internal ring for orchidopexy
vessels inguinal ring
Laparoscopic or Staged Fowler- Vanishing testis

Inguinal
inguinal Stephens no further
exploration
orchidopexy procedure steps
HYDROCELE
Background
Non-communicating hydroceles are found secondary to
minor trauma, testicular torsion, epididymitis, or varicocele
operation, or may appear as a recurrence after primary repair
of a communicating hydrocele.

A communicating hydrocele vacillates in size, usually relative
to activity. It is diagnosed by medical history and physical
investigation, the swelling is translucent, and transillumination
of the scrotum confirms the diagnosis. If there are any
doubts about intra-scrotal mass, ultrasound (US) should be
performed. Contralateral disease should be excluded.
Surgical Treatment
Surgical treatment of hydrocele is not indicated within the
first 12-24 months because of the tendency for spontaneous
resolution.
However, early surgery is indicated if there is suspicion
of a concomitant inguinal hernia or underlying testicular
pathology. There is no evidence that this type of hydrocele
risks testicular damage.
The surgical procedure consists of ligation of the patent
processus vaginalis via an inguinal incision, leaving the distal
stump open, whereas in hydrocele of the cord, the cystic
mass is excised or unroofed. Sclerosing agents should not
be used because of the risk of chemical peritonitis in the
communicating processus vaginalis peritonei.
The scrotal approach (Lord or Jaboulay technique) is used in

the treatment of a secondary non-communicating hydrocele.

Observe hydrocele for twelve months prior Strong
to considering surgical treatment in the
majority of infants.
Perform early surgery if there is suspicion of Strong
a concomitant inguinal hernia or underlying
testicular pathology.

Perform a scrotal ultrasound in case of Strong
doubt about the character of an intra-
scrotal mass.
Do not use sclerosing agents because of Strong
the risk for chemical peritonitis.
HYPOSPADIAS
Background
Hypospadias are usually classified according to the
anatomical location of the proximally displaced urethral
orifice:
• distal - anterior hypospadias (glanular, coronal or distal
penile);
• intermediate - middle (penile);
• proximal - posterior (penoscrotal, scrotal, perineal).
The pathology may be much more severe after skin release.
Patients with hypospadias should be diagnosed at birth.
The diagnostic evaluation also includes an assessment of
associated anomalies, which include cryptorchidism and open
processus vaginalis or inguinal hernia. Severe hypospadias
with unilaterally or bilaterally impalpable testis, or with
ambiguous genitalia, require a complete genetic and
endocrine work-up immediately after birth to exclude DSD,
especially congenital adrenal hyperplasia.
Trickling urine and ballooning of the urethra require
exclusion of meatal stenosis.
The length of the hypospadiac penis may be distorted by

penile curvature, penoscrotal transposition, or may be smaller
due to hypogonadism.
Differentiation between functionally necessary and

aesthetically feasible operative procedures is important for

therapeutic decision-making. As all surgical procedures carry
the risk of complications; thorough pre-operative counselling
of the caregivers is crucial. The therapeutic objectives are
to correct the penile curvature, to form a neourethra of an
adequate size, to bring the neomeatus to the tip of the glans,
if possible, and to achieve an overall acceptable cosmetic
appearance. This goal is achieved by using different surgical
techniques according to the individual findings.
Surgical Treatment
For repeat hypospadias repairs, no definitive guidelines can be
given.
Excellent long-term functional and cosmetic results can
be achieved after repair of anterior penile hypospadias. The
complication rate in proximal hypospadias repair is higher.
Figure 3 provides an algorithm for the management of
hypospadias.

Figure 3: Algorithm for the management of hypospadias
Diagnosis at birth Exclude DSD
No
Paediatric urologist
reconstruction
Reconstruction
required
Distal Proximal
Chordee No chordee
Urethral Urethral
plate cut plate preserved
Thiersch Duplay,
TIP, Mathieu, Two-stage,
MAGPI, tube-onlay Onlay, TIP
advancement Koyanagi repair
DSD = disorders of sex development; GAP = glans

approximation procedure; TIP = tubularised incised plate
urethroplasty; MAGPI = meatal advancement and
glanuloplasty incorporated.

MICROPENIS
Micropenis is defined as a small but otherwise normally
formed penis with a stretched length of less than 2.5 cm ±
standard deviation (SD) below the mean (Table 1).
Table 1: Length of the penis in boys

(according to Feldmann and Smith)
Age Mean ± SD (cm)
Newborns 3.5 ± 0.4
0-5 months 3.9 ± 0.8
6-12 months 4.3 ± 0.8
1-2 years 4.7 ± 0.8
2-3 years 5.1 ± 0.9
3-4 years 5.5 ± 0.9
4-5 years 5.7 ± 0.9
5-6 years 6.0 ± 0.9
6-7 years 6.1 ± 0.9
7-8 years 6.2 ± 1.0
8-9 years 6.3 ± 1.0
9-10 years 6.3 ± 1.0
10-11 years 6.4 ± 1.1
Adults 13.3 ± 1.6
VARICOCELE IN CHILDREN AND ADOLESCENTS

Background
Varicocele is unusual in boys under ten years of age, but
becomes more frequent at the beginning of puberty. Fertility
problems will arise in about 20% of adolescents with
varicocele. The adverse influence of varicocele increases with
time.

Testicular catch-up growth and improvement in sperm
parameters after varicocelectomy has been reported in
adolescents. Varicocele is mostly asymptomatic, rarely
causing pain at this age. It may be noticed by the patient or
caregivers, or discovered by the paediatrician at a routine visit.
Diagnosis and classification depends upon the clinical finding
and US investigation.
Surgical Treatment
Surgical intervention is based on ligation or occlusion of the
internal spermatic veins. Microsurgical lymphatic-sparing
repairs (microscopic or laparoscopic) are associated with
the lowest recurrence and complication rates. There is no
evidence that treatment of varicocele at paediatric age
will offer a better andrological outcome than an operation
performed later.
Conservative treatment and follow-up

During adolescence, testicular size should be checked
annually. After adolescence, repeated sperm analysis is
recommended. Figure 4 shows an algorithm for the diagnosis
of varicocele in children and adolescents, and Figure 5 shows
an algorithm for its treatment.

Figure 4: Algorithm for the diagnosis of varicocele in
children and adolescents
Varicocele in children
and adolescents
Physical examination Ultrasound

in the investigation
upright position
Venous
reflux Size
Grade I - Valsalva positive detected of the
Grade II - Palpable on Doppler testes
Grade III - Visible ultrasound

Figure 5: Algorithm for the management of varicocele in
children and adolescents
Varicocele in children
and adolescents
Surgery Conservative treatment
Indication Type Indication Type

• Small testis Microsurgical • Symmetrical • Measurement
(growth lymphatic-sparing testes of testicular
arrest) repair • Normal size (during
• Additional (microscopic spermiogram adolescence)
testicular or laparoscopic) (in older • Repeated
pathology adolescents) sperm analysis
• Bilateral (after
palpable adolescence)
varicocele
• Pathological
spermiogram
• Symptomatic
varicocele
URINARY TRACT INFECTIONS IN CHILDREN

Background
Urinary tract infections (UTIs) represent the most common
bacterial infection in children. In neonates, the symptoms
differ in many aspects from those in infants and children. The
prevalence is higher; there is a male predominance; infections
not caused by Escherichia coli are more frequent, and there is
a higher risk of urosepsis.
• Site: Lower urinary tract (cystitis) versus upper urinary tract

(pyelonephritis);

• Episode: first UTI versus unresolved infection, persistent
infection and re-infection;
• Severity: simple UTI versus severe UTI;
• Symptoms: asymptomatic bacteriuria versus symptomatic
UTI;
• Complicating factors: uncomplicated versus complicated
UTI.
Diagnosis includes a medical history, searching for clinical
signs and symptoms and a complete physical examination.
Urine sampling, analysis and culture

Urine sampling has to be performed before any antimicrobial
agent is administered. The technique for obtaining urine is
important to confirm or exclude UTI. Sampling in neonates,
infants and non-toilet-trained children:
• Plastic bag: (high incidence of false positive results
[85-99%]). Only helpful to exclude a UTI if the dipstick is
negative for leukocyte esterase and the culture results are
negative, otherwise the UTI has to be confirmed by a more
specific method.
• Clean-catch urine collection: has a false-positive rate of
5% and false-negative rate of 12% and the contamination
rate is higher compared to supra-pubic bladder aspiration
(SPA).
• Bladder catheterisation: In female infants and in neonates,
this technique may be an alternative to SPA, however with
a higher contamination rate.
• Supra-pubic bladder aspiration: This is the most sensitive
method to obtain an uncontaminated urine sample in
non-toilet trained children.
• Midstream urine in toilet-trained, children who can void on
command, could be an acceptable technique for obtaining
urine after cleaning the urethral meatus and perineum.

Urinalysis:
• Dipsticks: are ready to use and helpful when the result is
positive, because it is highly specific.
• Microscopy: can be used after centrifugation as well as in
uncentrifuged urine and has been demonstrated to be sen-
sitive for UTI. This is rarely done in an outpatient setting.
• Flow imaging analysis technology: is being increasingly
used to classify particles in uncentrifuged urine specimens
and correlates well with manual methods.
• Urine culture: is generally not necessary after negative
results for dipstick, microscopic or automated urinalysis. If
the dipstick result is positive, confirmation by urine culture
is strongly recommended.
Pyuria without bacteriuria (sterile pyuria) may be due to

incomplete antibiotic treatment, urolithiasis, or foreign bodies
in the urinary tract, and infections caused by Mycobacterium
tuberculosis or Chlamydia trachomatis.
Table 2: Criteria for UTI in children
Urine specimen Urine specimen Urine specimen

from suprapubic from bladder from midstream
bladder puncture catheterisation void
Any number of ≥ 103 - 105 cfu/mL ≥ 104 cfu/mL with
cfu/mL (at least 10 symptoms
identical colonies) ≥ 105 cfu/mL with-
out symptoms
Imaging
Ultrasound (US): of the kidneys and bladder as soon as
possible is advised in infants with febrile UTI to exclude
obstruction of the upper and lower urinary tract and post-void
residual urine should be measured in toilet-trained children to
exclude voiding abnormalities as a cause of UTI.

Radionuclide scanning: changes in dimercaptosuccinic acid
(DMSA) clearance during acute UTI (up to four to six weeks)
indicating pyelonephritis and renal scars can be detected after
three to six months. This correlates well with the presence of
dilating reflux and the risk of further pyelonephritis episodes,
breakthrough infections and future renal scarring.
Voiding cystourethrography (VCUG): is best practice to
exclude or confirm vesicoureteral reflux, due to the risk of
renal scarring, VCUG is recommended after the first episode
of febrile UTI in boys and girls depending on sex, age and
clinical presentation (see Figure 6). Another option is doing
DMSA first, followed by VCUG if there is renal cortical uptake
deficiency after UTI.
Bladder and bowel dysfunction (BBD) are risk factors for

which each child with UTI should be screened for upon
presentation. If there are signs of BBD at infection-free
intervals, further diagnosis and effective treatment are
strongly recommended.
Status of circumcision should be checked in boys
and treatment of the phimosis considered in those with
pyelonephritis.
Management
Administration route: the choice between oral and parenteral
therapy should be based on patient age; clinical suspicion of
urosepsis; illness severity; refusal of fluids, food and/or oral
medication; vomiting; diarrhoea; non-compliance; and
complicated pyelonephritis (e.g. urinary obstruction). Febrile
UTI in early infancy should be treated by i.v. fluids and
antibiotics and under close monitoring within the hospital.
Duration of therapy: outcomes of short courses (one to three
days) are inferior to those of seven to fourteen days. In late
infancy, oral therapy with a third-generation cephalosporin
(e.g. cefixime or ceftibuten) is equivalent to the usual two to

four days intravenous therapy followed by oral treatment in
uncomplicated UTI’s. In complicated UTI parenteral treatment
with broad-spectrum antibiotics is preferred.
Figure 6: Algorithm for the management of a first febrile UTI
First febrile UTI
Ultrasound upper and

lower urinary tract
Suspicion of VUR and/or Upper tract dilatation/

No pathological findings
pyelonephritis hydronephrosis
Complicated UTI/close
Boys > 12 months Infant/girl monitoring i.v. antibiotic
treatment
Critical
Imaging Good clinical
Exclusion of status or no
after response
reflux/VCUG/DMSA response
recurrent
infections
Further Consider
evaluation of transient
upper tract urinary
function diversion
(renal
scan/MRI)
Exclusion of
VUR (VCUG)
Toilet trained children: exclusion of BBD
BBD = Bladder Bowel Dysfunction; DMSA = technetium99-

labelled dimercaptosuccinic acid; MRI = magnetic resonance
imaging; UTI = urinary tract infection; VCUG = voiding
cystourethrography; VUR = vesicoureteral reflux;
i.v. = intravenous.

Monitoring of UTI
Urine usually becomes sterile after 24 hours, and leukocyturia
disappears within three to four days. Normalisation of body
temperature can be expected within 24-48 hours after the
start of therapy in 90% of cases. In patients with prolonged
fever and failing recovery, treatment-resistant uropathogens
or the presence of congenital uropathy or acute urinary
obstruction should be considered. Immediate US examination
is recommended.
Procalcitonin (among other laboratory inflammatory

parameters such as C-reactive protein and leukocyte count)
is a reliable serum marker for early prediction of renal
parenchymal inflammation. In patients with febrile UTI, serum
electrolytes and blood cell counts should be obtained.

Take a medical history, assess clinical Strong
signs and symptoms and perform a
physical examination to diagnose children
suspected of having a urinary tract
infection (UTI).
Exclude bladder and bowel dysfunction Strong
(BBD) in any child with febrile and/or
recurrent UTI and do not delay diagnosis
and treatment of BBD.
The most effective way to collect an Strong
uncontaminated urine sample in an infant
is through suprapubic bladder aspiration,
bladder catheterisation is an alternative
with a higher contamination rate.

Do not use plastic bags for urine sampling Strong
in non-toilet-trained children since it has
a high risk of false-positive results. Clean
catch urine is an acceptable technique for
toilet-trained children.
Urinalysis by dipstick yields rapid results, Weak
but it should be used with caution.
Microscopic investigation is the standard
method of assessing pyuria after
centrifugation. Using flow imaging analysis,
the numbers of white blood cells, squamous
epithelial cells and red cells correlate well
with manual methods.
The choice between oral and parenteral Strong
therapy should be based on patient age;
clinical suspicion of urosepsis; illness
severity; refusal of fluids, food and/or oral
medication; vomiting; diarrhoea; non-
compliance; complicated pyelonephritis.
Treat UTIs with four to seven day courses of Strong
oral or parenteral therapy.
Offer long-term antibacterial prophylaxis in Weak
case of high susceptibility to UTI and risk
of acquired renal damage and lower urinary
tract symptoms.
Treat complicated UTI, with broad- Weak
spectrum antibiotics (parenteral).
In infants with febrile UTI, use renal and Strong
bladder ultrasound to exclude obstruction
of the upper and lower urinary tract.

In all infants, exclude vesicoureteral reflux Strong
(VUR) after the first episode of febrile UTI,
using voiding cystourethography (VCUG)
or a dimercaptosuccinic acid (DMSA) scan
first (in case of a positive DMSA-scan,
follow-up with VCUG). In boys more than
one year of age, exclude VUR after the
second febrile UTI.
MONOSYMPTOMATIC NOCTURNAL ENURESIS -

BEDWETTING
Background
Monosymptomatic nocturnal enuresis is incontinence during
the night. Any wetting during sleep above the age of five years
is considered nocturnal enuresis. It is important to note that
there is a single symptom only. Due to an imbalance between
night-time urine output and night-time bladder capacity, the
bladder can easily become full at night, and the child will
either wake-up to empty the bladder or will void during sleep.
A voiding diary, registering the day-time bladder function and
the night-time urine output will help guide the treatment.
Measuring the day-time bladder capacity gives an estimate
of bladder capacity to compare with normal values for age.
Figure 7 presents an algorithm for the diagnosis and
treatment of monosymptomatic nocturnal enuresis.

Figure 7: Algorithm for the assessment and management of
nocturnal enuresis
Child ≥ 5 years with nocturnal enuresis
2 weeks Upon indication

night time • Urine
urine microscopy
Detailed production • Uroflow-metry
2 days
questions for Physical recording • Ultrasound
daytime
day -time exam and (= weight • ENT referral
voiding and • Psychologist
symptoms urinanalysis night time
drinking diary referral
diapers +
morning first
voided
volume)
Supportive measures (not a treatment) (max 4 weeks)

• Normal and regular drinking habits
• Regular voiding and bowel habits
• Monitor night time production (weight diapers)
Child + caregivers seek a treatment
Nocturnal enuresis
wetting alarm
desmopressin
treatment
+/ - anticholinergics
with regular
follow-up
If no improvement (< 4 weeks) OR Lack of compliance

+
Re-evaluate
ENT = ear, nose, throat

VESICOURETERIC REFLUX IN CHILDREN
Background
Vesicoureteric reflux presents with a wide range of severities,
and the majority of reflux patients will not develop renal scars
and probably will not need any intervention. The main goal in
management is the preservation of kidney function.
The diagnostic work-up should evaluate the overall health and
development of the child. A basic diagnostic work-up includes
a detailed medical history (including family history, and
screening for lower urinary tract dysfunction [LUTD]), physical
examination including blood pressure measurement, urinaly-
sis (assessing proteinuria), urine culture, and serum creatinine
in patients with bilateral renal parenchymal abnormalities.
Prenatally diagnosed hydronephrosis

Ultrasound of the kidney and bladder is the first standard
evaluation tool for children with prenatally diagnosed
hydronephrosis.
It should be delayed until the end of first week after birth
because of early oliguria in the neonate. It is essential to
evaluate the bladder, as well as the kidneys.

Inform parents of children with Strong
vesicoureteric reflux (VUR) that siblings
and offspring have a high prevalence of
VUR.
Use renal ultrasound (US) for screening of Strong
sibling(s).
Use voiding cystourethrography if there Weak
is evidence of renal scarring on US or a
history of urinary tract infection.

Do not screen older toilet-trained children Weak
since there is no added value in screening
for VUR.
Conservative therapy
The objective of conservative therapy is prevention of febrile
UTI. It is based on the understanding that:
• VUR resolves spontaneously, mostly in young patients with
low-grade reflux. However, spontaneous resolution is low in
bilateral high-grade reflux.
• VUR does not damage the kidney when patients are free of
infection and have a normal lower urinary tract function.
• There is no evidence that small scars can cause
hypertension, renal insufficiency or problems during
pregnancy and in the long-term.
• The conservative approach includes watchful waiting,
intermittent or continuous antibiotic prophylaxis, and
bladder rehabilitation in those with LUTD.
• Circumcision in early infancy may be considered as part
of the conservative approach, because it is effective in
reducing the risk of infection in normal children.
Surgical Treatment
Surgical treatment comprises endoscopic injection of bulking
agents or ureteral re-implantation.
Subureteric injection of bulking agents: Due to the availability

of biodegradable substances, endoscopic subureteric
injection of bulking agents has become an alternative to long-
term antibiotic prophylaxis and surgical intervention.
Open surgical techniques: Overall, all surgical procedures offer

very high and similar success rates for correcting VUR.

Laparoscopy: A laparoscopic approach cannot be
recommended as a routine procedure. It can be offered as an
alternative to the caregivers in centres where there is enough
experience.

Initially treat all patients diagnosed within Weak
the first year of life with continuous
antibiotic prophylaxis, regardless of the
grade of reflux or presence of renal scars.
Offer immediate, parenteral antibiotic Strong
treatment for febrile breakthrough
infections.
Offer definitive surgical or endoscopic Weak
correction to patients with frequent
breakthrough infections.
Offer open surgical correction to patients Strong
with persistent high-grade reflux and
endoscopic correction for lower grades of
reflux.
Initially manage all children presenting at Strong
age one to five years conservatively.
Offer surgical repair to children above the Weak
age of one presenting with high-grade
reflux and abnormal renal parenchyma.
Offer close surveillance without antibiotic Strong
prophylaxis to children presenting with
lower grades of reflux and without
symptoms.

Ensure that a detailed investigation for the Strong
presence of lower urinary tract dysfunction
(LUTD) is done in all and especially in
children after toilet-training. If LUTD is
found, the initial treatment should always
be for LUTD.
Offer surgical correction, if parents Strong
prefer definitive therapy to conservative
management.
Select the most appropriate management Weak
option based on:
• the presence of renal scars;
• clinical course;
• the grade of reflux;
• ipsilateral renal function;
• bilaterality;
• bladder function;
• associated anomalies of the urinary
tract;
• age and gender;
• compliance;
• parental preference.
Refer to Table 3 for risk factors and follow-
up.
In high-risk patients who already have Strong
renal impairment, a more aggressive, multi-
disciplinary approach is needed.

EAU/ESPU Paediatric Urology Guidelines (ISBN 978-94-92671-01-1),
available at their website, http://www.uroweb.org/guidelines.

Table 3: Management and follow-up according to different risk groups
Risk Presentation Initial treatment

Groups
High Symptomatic male Initial treatment is
or female patients always for LUTD with
after toilet-training CAP; intervention may
with high-grade reflux be considered in cases
(grades IV-V), abnormal of BT infections or
kidneys and LUTD persistent reflux
High Symptomatic male or Intervention should be
female patients after considered
toilet-training with
high-grade reflux (grade
IV-V), abnormal kidneys
and no LUTD
Moderate Symptomatic male or CAP is the initial
female patients before treatment. Intervention
toilet-training, with may be considered in
high-grade reflux and cases of BT infections
abnormal kidneys or persistent reflux
Moderate Asymptomatic patients Initial treatment is
(PNH or sibling) with always for LUTD with
high-grade reflux and CAP. Intervention may
abnormal kidneys be considered in cases
of BT infections or
persistent reflux
Moderate Symptomatic male or Initial treatment is
female patients after always for LUTD with
toilet-training, with CAP. Intervention may
high-grade reflux and be considered in cases
normal kidneys with of BT infections or
LUTD persistent reflux

Comment Follow-up
Greater possibility of earlier More aggressive follow-

intervention up for UTI and LUTD;
full re-evaluation after 6
months
Open surgery has better results Post-operative VCUG on

than endoscopic surgery indication only; follow-up
of kidney status until after
puberty
Spontaneous resolution is Follow-up for UTI/

higher in males hydronephrosis; full
re-evaluation after 12-24
months
Follow-up for UTI/

hydronephrosis; full
re-evaluation after 12-24
months
In case of persistent LUTD, Follow-up for UTI and

despite urotherapy, intervention LUTD, kidney status;
should be considered. The full re-evaluation after
choice of intervention is successful urotherapy
controversial

Moderate Symptomatic male or Choice of treatment
female patients after is controversial.
toilet-training with low- Endoscopic treatment
grade reflux, abnormal may be an option.
kidneys with or without LUTD treatment should
LUTD be given if needed
Moderate All symptomatic Initial treatment is
patients with normal always for LUTD with or
kidneys, with low-grade without CAP
reflux, with LUTD
Low All symptomatic No treatment or CAP
patients with normal
kidneys, with low-grade
reflux, with no LUTD
Low All asymptomatic No treatment or CAP in
patients with normal infants
kidneys with low-grade
reflux
CAP = continuous antibiotic prophylaxis; LUTD = lower

urinary tract dysfunction; PNH = prenatal diagnosed
hydronephrosis; UTI = urinary tract infection; VCUG = voiding
cystourethrography.

Follow-up for UTI, LUTD,
and kidney status until
after puberty
Follow-up for UTI and

LUTD
If no treatment is given, Follow-up for UTI

caregivers should be informed
about risk of infection
If no treatment is given, Follow-up for UTI

caregivers should be informed
about risk of infection

EAU GUIDELINES ON
UROLOGICAL TRAUMA
N.D. Kitrey (Chair), N. Djakovic, F.E. Kuehhas, N. Lumen,

E. Serafetinidis, D.M. Sharma
Guidelines Associates: Y. Abu-Ghanem, A. Sujenthiran
Introduction
Genito-urinary trauma is seen in both sexes and in all age
groups, but is more common in males. Traumatic injuries are
classified according to the basic mechanism into penetrating
and blunt.
Penetrating trauma is further classified according to the

velocity of the projectile:
1. High-velocity projectiles (e.g. rifle bullets - 800-1000 m/sec).
2. Medium-velocity (e.g. handgun bullets - 200-300 m/sec).
3. Low-velocity items (e.g. knife stab).
High-velocity weapons inflict greater damage as the bullets

transmit large amounts of energy to the tissues, resulting in
damage to a much larger area then the projectile tract itself. In
lower velocity injuries, the damage is usually confined to the
tract of the projectile.
Blast injury is a complex cause of trauma, it commonly

includes both blunt and penetrating trauma, and may also be
accompanied by burn injuries.
338 Urological Trauma

Initial evaluation and management
The first priority is stabilisation of the patient and treatment of
associated life-threatening injuries. A direct history is obtained
from the patient (if conscious) or from witnesses/emergency
personnel (if patient is unconscious and/or seriously injured).
In penetrating injuries, assess size of the weapon in stabbings,

and the type and calibre of the weapon used in gunshot
wounds. The medical history should be as detailed as possible.
It is important to recognise the high risk of hepatitis B and C
infection in trauma patients and take appropriate precautions.
In any penetrating trauma, tetanus vaccination should be
considered according to the patient’s vaccination history and
nature of the wound.
Renal Trauma
Renal injuries are associated with young age and male gender,
the incidence is approximately 4.9 per 100,000 of the popula-
tion. The most commonly used classification system is that
of the American Association for the Surgery of Trauma. This
validated system has clinical relevance and helps to predict
the need for intervention. It also predicts morbidity after blunt
or penetrating injury and mortality after blunt injury.

Assess haemodynamic stability upon Strong
admission.
Record past renal surgery, and known pre- Strong
existing renal abnormalities (ureteropelvic
junction obstruction, large cysts, lithiasis).
Test for haematuria in a patient with Strong
suspected renal injury.
Urological Trauma 339

Perform a contrast enhanced CT scan in Strong
blunt trauma patients with;
• visible haematuria;
• non-visible haematuria with
haemodynamic instability;
• a history of rapid deceleration injury
and/or significant associated injuries;
• penetrating abdominal or lower
thoracic injury.
Perform CT delayed phase images in case Strong
of haemodynamic stability.
Management

Manage stable patients with blunt renal Strong
trauma conservatively with close
monitoring of vital signs.
Manage isolated grade 1-3 stab and low- Strong
velocity gunshot wounds in stable patients,
expectantly.
Use angioembolisation for active renal Strong
bleeding if there are no other indications
for immediate laparotomy.
Proceed with renal exploration in the Strong
presence of:
• persistent haemodynamic instability;
• expanding or pulsatile peri-renal
haematoma;
• grade 5 vascular injury;
• exploration for associated injuries.
Attempt renal reconstruction if Weak
haemorrhage is controlled and there is
sufficient viable renal parenchyma.

Suspected adult blunt
renal trauma*
Determine haemodynamic stability

Stable Unstable
after primary resuscitation
Non-visible haematuria Visible haematuria Emergency laparotomy/One-shot IVP
Rapid deceleration Contrast enhanced

Normal IVP
injury or major spiral CT scan with Abnormal IVP,
associated injuries delayed images † pulsatile
or expanding
Observation haematoma
Grade 1 -2 Grade 3 Grade 4-5
Renal exploration
Parenchymal Vascular (reconstruction or
nephrectomy)‡
Observation Observation, Angiography
bed rest, serial Ht, and selective
antibiotics angioembolisation Observation, Angiography
bed rest, serial Ht, and selective
Figure 1: Evaluation of blunt renal trauma in adults
antibiotics angioembolisation
Associated injuries requiring laparotomy

Figure 2: Evaluation of penetrating renal trauma in adults
Evaluation of penetrating
renal trauma*
Determine haemodynamic stability
Stable Unstable
Contrast enhanced Emergency

spiral CT scan with laparotomy
delayed images†
Renal exploration
Grade 1 - 2 Grade 3 Grade 4 - 5 (reconstruction or
nephrectomy) ‡
Observation, Associated
bed rest, serial Ht, injuries requiring
antibiotics laparotomy
Angiography
and selective
angioembolisation
* Suspected renal trauma results from reported mechanism

of injury and physical examination.
† Renal imaging: CT scans are the gold standard for
evaluating blunt and penetrating renal injuries in stable

patients. In settings where CT is not available, the urologist
should rely on other imaging modalities (IVP, angiography,
radiographic scintigraphy, MRI).
‡ Renal exploration: Although renal salvage is a primary goal
for the urologist, decisions concerning the viability of the

organ and the type of reconstruction are made during the
operation.
CT = computed tomography; Ht = haematocrit;
IVP = intravenous pyelography.

Post-operative care, follow-up and complications

Repeat imaging in case of fever, worsening Strong
flank pain, or falling haematocrit.
Follow-up approximately three months Weak
after major renal injury with:
• physical examination;
• urinalysis;
• individualised radiological investigation
including nuclear scintigraphy;
• serial blood pressure measurements;
• renal function tests.
Iatrogenic renal injuries

• Iatrogenic renal injuries are procedure-dependent (1.8-15%).
• Significant injury requiring intervention is rare; the most
common injuries are vascular.
• Renal allografts are more susceptible.
• Injuries occurring during surgery should be rectified
immediately.
• Symptoms suggestive of a significant injury require
investigation.
The recommendations for iatrogenic renal injuries are the

same as those for follow-up.
Ureteral Trauma
Ureteral injuries are quite rare - most are iatrogenic. They
are often missed intra-operatively, usually involve the lower
ureter, and may result in severe sequelae. Risk factors include
advanced malignancy, prior surgery or irradiation - i.e.
conditions which alter the normal anatomy. Pre-operative
prophylactic stents do not prevent ureteral injury, but may

assist in its detection. External ureteral trauma usually
accompanies severe abdominal and pelvic injuries. Gunshot
wounds account for the majority of penetrating ureteral
trauma, while motor vehicle accidents account for most blunt
injuries.
• A high index of suspicion of ureteral injury should be
maintained as the majority of cases are diagnosed late,
predisposing the patient to pain, infection, and renal
function impairment.
• Haematuria is an unreliable indicator.
• Extravasation of contrast material in computed tomo-
graphy (CT) is the hallmark sign of ureteral trauma.
• In unclear cases, a retrograde or antegrade urography is
required for confirmation.
Management

Visually identify the ureters to prevent Strong
ureteral trauma during abdominal and
pelvic surgery.
Beware of concomitant ureteral injury in Strong
all abdominal penetrating trauma, and in
deceleration-type blunt trauma.
Use pre-operative prophylactic stents in Strong
high-risk cases.
The type of repair procedure depends on the site of the injury

(Table 2), and should follow the principles outlined in Table 3.

Table 2: Ureteral reconstruction options by site of injury
Site of injury Reconstruction options
Upper ureter Uretero-ureterostomy
Transuretero-ureterostomy
Uretero-calycostomy
Mid ureter Uretero-ureterostomy
Transuretero-ureterostomy
Ureteral re-implantation and a Boari flap
Lower ureter Ureteral re-implantation
Ureteral re-implantation with a psoas hitch
Complete Ileal interposition graft
Autotransplantation
Table 3: Principles of surgical repair of ureteral injury

Debridement of necrotic tissue
Spatulation of ureteral ends
Watertight mucosa-to-mucosa anastomosis with absorbable
sutures
Internal stenting
External drain
Isolation of injury with peritoneum or omentum
Bladder Trauma
Bladder injuries can be due to external (blunt or penetrating)
or iatrogenic trauma. Iatrogenic trauma is caused by external
laceration or internal perforation (mainly during transurethral
resection of the bladder). Blunt bladder injuries are strongly
associated with pelvic fractures. Bladder injuries are classified
as extraperitoneal, intraperitoneal or combined.

Clinical signs and symptoms
External trauma
• Cardinal sign: visible haematuria.
• Others: abdominal tenderness, inability to void, bruises
over the suprapubic region, and abdominal distension (in
case of urinary ascites).
• Penetrating bladder injury: entrance and exit wounds in
lower abdomen or perineum.
• Bloody urethrorrhagia: suspect concomitant urethral injury.
Iatrogenic trauma
• External perforation: extravasation of urine, visible
laceration, clear fluid in the surgical field, appearance of
the bladder catheter, and blood and/or gas (in case of
laparoscopy) in the urine bag.
• Internal perforation: fatty tissue or bowel between detrusor
muscle fibres, inability to distend the bladder, low return of
irrigation fluid and/or abdominal distension.
• Post-operative symptoms of unrecognised bladder
perforation: haematuria, lower abdominal pain, abdominal
distension, ileus, peritonitis, sepsis, urine leakage from the
wound, decreased urinary output, and increased serum
creatinine.
Imaging – Cystography and Cystoscopy

Perform cystography in case of suspected Strong
iatrogenic bladder injury in the post-
operative setting.
Perform cystography in the presence of Strong
visible haematuria and pelvic fracture.

Perform cystography with active retrograde Strong
filling of the bladder with dilute contrast.
Use cystoscopy to rule out bladder injury Strong
after suburethral sling procedure by the
retropubic route.
Do not perform cystography to assess Weak
bladder wall healing after repair of a simple
injury in a healthy patient.
Perform cystography to assess bladder wall Strong
healing after repair of a complex injury or in
case of risk factors for wound healing.
Management
• Surgical repair (two-layer vesicorraphy)
• Conservative management (urinary catheter)

Manage a blunt extraperitoneal bladder Strong
injury operatively in cases of bladder neck
involvement and/or associated injuries that
require surgical intervention.
Manage uncomplicated blunt extraperito- Weak
neal bladder injury conservatively.
Manage intraperitoneal injuries caused by Strong
blunt trauma by surgical exploration and
repair.
Manage small uncomplicated iatrogenic Weak
intraperitoneal bladder injuries
conservatively.

Urethral Trauma
• Injuries to the anterior urethra (AU) are caused by trauma
during sexual intercourse (associated with penile fracture),
penetrating trauma, placement of penile constriction
bands, and from iatrogenic trauma e.g. endoscopic
instruments, catheterisation.
• Injuries to the posterior urethra (PU) occur with pelvic
fractures, mostly as a result of motor vehicle accidents.
• The male PU is injured in 4-19% of pelvic fractures, and the
female urethra in 0-6% of all pelvic fractures.
• The combination of straddle fractures with diastasis of the
sacroiliac joint has the highest risk of urethral injury.
• Injuries can vary from simple stretching to partial rupture
to complete disruptions.
• Urethral injuries in women are rare.
• Blood at the external urethral meatus is the most common
clinical sign, and indicates the need for further diagnostic
work up.
• Although non-specific, haematuria on a first voided
specimen may indicate urethral injury. The amount of
urethral bleeding correlates poorly with the severity of
injury.
• Pain on urination or inability to void may indicate
disruption.
• Blood at the vaginal introitus is present in more than 80%
of female patients with pelvic fractures and co-existing
urethral injuries.
• Rectal examination may reveal a “high riding” prostate.
However, this is an unreliable finding. Blood on the
examination finger is suggestive of a rectal injury
associated with pelvic fracture.
• Urethral bleeding or urinary extravasation can cause penile
and scrotal swelling and haematoma.

• Retrograde urethrography is the gold standard for
evaluating urethral injury and urethral catheterisation
should be avoided until the urethra is imaged.
• In an unstable patient, however, an attempt can be made
to pass a urethral catheter (gently, by someone with
urological experience). If this is not possible, a suprapubic
catheter is inserted and a retrograde urethrogram is
performed later.
• In females, urethroscopy may be an important adjunct for
the identification and staging of urethral injuries.
Management
Urethral trauma

Evaluate urethral injuries with flexible Strong
cystoscopy and/or retrograde urethrography.
Treat blunt anterior urethral injuries by Strong
suprapubic diversion.
Treat partial posterior urethral ruptures by Strong
urethral or suprapubic catheterisation.
Perform early endoscopic re-alignment Weak
when feasible.
Manage complete posterior urethral disrup- Strong
tion with suprapubic diversion and deferred
(at least three months) urethroplasty.
Iatrogenic urethral trauma

Provide appropriate training to reduce the Strong
risk of traumatic catheterisation.
Keep duration of catheterisation to a Strong
minimum.

Genital Trauma
Of all genito-urinary injuries, one-third to two-thirds involve
the external genitalia and are much more common in males
due to anatomical differences, increased frequency of road
traffic accidents, physical sports, violent crime, and war-fight-
ing. Eighty percent is blunt trauma, 20% is due to penetrating
injuries.
• Urinalysis should be performed.
• Visible- and/or non-visible haematuria requires a retrograde
urethrogram in males, whilst cystoscopy should be
considered in females.
• In women with genital injuries and blood at the vaginal
introitus, further gynaecologic investigation to exclude
vaginal injury is required.
• In cases of suspected sexual abuse gynaecologic and
forensic support and advice is necessary. The emotional
situation and privacy of the patient must be respected.
Blunt penile trauma

Usually results from trauma to the erect penis during sexual
intercourse or masturbation.
Penile fracture
• Sudden cracking or popping sound, pain and immediate
detumescence.
• Local swelling of the penile shaft is seen and this may
extend to the lower abdominal wall.
• The rupture of the tunica may be palpable.
• Thorough history and examination confirms diagnosis.
• Imaging ultrasound (US) or magnetic resonance imaging
(MRI) may be useful.

Management
• Subcutaneous haematoma, without associated rupture of
the cavernosal tunica albuginea does not require surgical
intervention. Non-steroidal analgesics and ice-packs are
recommended.
• In penile fracture, early surgical intervention with closure
of the tunica albuginea is recommended.
• Intra-operative flexible cystoscopy is useful to diagnose
urethral injury and to further localise tunical damage.
• Conservative management of penile fracture is not
recommended.
Penetrating penile trauma

• Rarely seen in isolation.
• Due to gunshot/knife injury, animal or human bites, assault
and industrial or self-inflicted mutilation.
• Non-operative management is recommended in small
superficial injuries with intact Buck’s fascia.
• More significant injuries require surgical exploration and
debridement of necrotic tissue.
• In extended injuries of the penis, primary alignment of
the disrupted tissues may allow for acceptable healing
because of the robust penile blood supply.
• In avulsion of the penis, resuscitate the patient and
attempt re-implantation of the penis (if not too badly
damaged) - ideally microsurgically.
Blunt scrotal trauma

• May result in testicular dislocation, haematocoele,
testicular rupture and/or scrotal haematoma.
• Dislocation of the testicle is rare. Treat by manual replace-
ment and secondary orchidopexy. If manual repositioning
cannot be performed, immediate orchidopexy is indicated.
• If haematocele is smaller than three times the size of the
contralateral testis – conservative management.

• If large haematocele - explore.
• If testicular rupture suspected, explore, evacuate clot and
any necrotic testicular tubules and close the tunica
albuginea.
Penetrating scrotal trauma

• Surgical exploration with conservative debridement of
nonviable tissue.
• Primary reconstruction of testis and scrotum can be
performed in most cases.
• In complete disruption of the spermatic cord, re-alignment
without vaso-vasostomy may be considered.
• In extensive destruction of the tunica albuginea,
mobilisation of a free tunica vaginalis flap can be
performed for testicular closure.
• If reconstruction cannot be achieved, orchiectomy is
indicated.
• In improvised explosive device blast injury, the extensive
loss of genital tissue often requires complex and staged
reconstructive surgical procedures.
Genital trauma in females

• In blunt trauma to the external genitalia, imaging studies of
the pelvis with US, CT, or MRI should be performed.
• Vulvar haematomas usually do not require surgical
intervention, but in massive vulvar haematoma or
haemodynamically unstable patients, surgical intervention,
lavage and drainage is indicated.
• In vulvar laceration, suturing after conservative
debridement is indicated with concomitant primary repair
of any associated vaginal injuries.
Polytrauma, Damage Control and Mass Casualty Events

Urological trauma is often associated with significant and
higher priority injuries in the polytraumatised patient. Damage

control principles govern the management of the severely
injured patient and urologists need to understand their role in
the context of polytrauma.
Damage control is a three-phase approach - rapid control of

haemorrhage and wound contamination, resuscitation in the
intensive care unit, and delayed definitive surgery.
Procedures should be directed at the rapid control of

bleeding, debridement of dead and devitalised tissue, and
minimising urinary extravasation by simple diversionary
measures.
A mass casualty event is one in which the number of injured

people is significantly higher than the number of healthcare
providers available. Examples include the collapse of buildings
or bridges, earthquakes, floods, tsunamis, train collisions,
aircraft catastrophes, civilian terrorism.
Triage sorts patients into four groups:

1. Patients with life-threatening injuries that require
immediate intervention, presenting with airway
compromise, breathing failure and/or circulatory
compromise from ongoing external haemorrhage.
2. Patients with severe but non-life-threatening injuries, in
whom treatment can be acceptably delayed: major
fractures, vascular injuries of the limbs and large soft tissue
wounds.
3. ‘Walking wounded’ with minimal injuries.
4. Patients who are so severely injured that treatment
would require allocation of resources and time that
would deny other, more salvageable patients, timely care.
These patients are given minimal or no treatment, and
re-evaluated when resources become available. There is
no absolute definition for this group because triage is

individualised according to the number and severity of
casualties related to the available resources.
Principles for urological consultations to follow during a mass

casualty scenario:
• Rule out under-triage by the surgeon in charge, and
perform a rapid primary survey of every patient.
• Avoid unnecessary imaging procedures such as CT scans
and retrograde urethrography. These procedures should be
performed later, after mass casualty protocols have been
suspended.
• Treat unstable patients who are to have surgery using
damage control principles.
• Stable patients with suspected renal injuries should be
transferred to the surgical ward without imaging
procedures. Re-evaluate if there is any change in their
haemodynamic status, or when possible as dictated by the
constraints of the mass casualty event. Patients managed
in this delayed fashion should be treated according to
traditional trauma management protocols.
• ‘Minimal acceptable’ procedures should be performed
in order to transfer patients to the surgical wards, e.g.
suprapubic drainage of the bladder when bladder or
urethral injuries are suspected, clamping and ligation of
bleeding vessels from wounds to the external genitalia, etc.


EAU GUIDELINES ON
CHRONIC PELVIC PAIN
D. Engeler (Chair), A.P. Baranowski, J. Borovicka, A.M. Cottrell,

P. Dinis-Oliveira, S. Elneil, J. Hughes, E.J. Messelink (Vice-chair),
A.C. de C. Williams
Guidelines Associates: B. Parsons, S. Goonewarden
Introduction
The EAU Guideline for Chronic Pelvic Pain plays an important
role in the process of consolidation and improvement of care
for patients with abdominal and pelvic pain. From both
literature and daily practice it has become clear that
abdominal and pelvic pain are areas still under development.
The EAU Guideline aims to expand the awareness of
caregivers in the field of abdominal and pelvic pain and to
assist those who treat patients with abdominal and pelvic
pain in their daily practice. The guideline is a useful instrument
not only for urologists, but also for gynaecologists, surgeons,
physiotherapists, psychologists and pain doctors.
This pocket version aims to synthesise the important clinical

messages described in the full text and is presented as a
series of ‘strength rated recommendations’, which follow
the standard for levels of evidence used by the EAU (see
Introduction chapter of the EAU Guidelines book and online at
the EAU website http://www.uroweb.org/guideline/).
Chronic Pelvic Pain 355

Table 1: Classification of chronic pelvic pain syndromes
Axis I Axis II Axis III
Region System End-organ as pain syndrome as identified
from Hx, Ex and Ix
Chronic Specific Urological Prostate

pelvic disease Bladder
pain associated
pelvic pain Scrotal
Testicular
OR Epididymal
Penile
Pelvic pain Urethral
syndrome Post-vasectomy
Gynaecological Vulvar
Vestibular
Clitoral
Endometriosis associated
CPPS with cyclical exacerbations
Dysmenorrhoea
Gastrointestinal Irritable bowel
Chronic anal
Intermittent chronic anal
Peripheral nerves Pudendal pain syndrome
Sexological Dyspareunia
Pelvic pain with sexual dysfunction
Psychological Any pelvic organ
Musculo-skeletal Pelvic floor muscle

Abdominal muscle
Spinal
Coccyx
356 Chronic Pelvic Pain

Axis IV Axis V Axis VI Axis VII Axis VIII
Referral Temporal Character Associated Psychological
character- characteristics symptoms symptoms
istics
Suprapubic ONSET Aching UROLOGICAL ANXIETY
Inguinal Acute Burning Frequency About pain
Urethral Chronic Stabbing Nocturia or putative
Penile/clitoral Electric Hesitance cause of pain
Perineal ONGOING Dysfunctional flow
Rectal Sporadic Urgency Catastrophic
Back Cyclical Incontinence thinking about
Buttocks Continuous pain
Thighs GYNAECOLOGICAL
TIME Menstrual DEPRESSION
Filling Menopause Attributed to
Emptying pain or impact
Immediate post GASTROINTESTINAL of pain
Late post Constipation
Diarrhoea Attributed to
TRIGGER Bloatedness other causes
Provoked Urgency
Spontaneous Incontinence Unattributed
NEUROLOGICAL PTSD
Dysaesthesia SYMPTOMS
Hyperaesthesia Re-experiencing
Allodynia Avoidance
Hyperalegesie
SEXOLOGICAL
Satisfaction
Female dyspareunia
Sexual avoidance
Erectile dysfunction
Medication
MUSCLE
Function impairment
Fasciculation
CUTANEOUS
Trophic changes
Sensory changes

Chronic pelvic pain syndromes
Classification
Much debate over the classification of chronic pelvic pain
(CPP) has occurred, is ongoing and will continue in the future.
Classification involves three aspects of defining a condition:
phenotyping, terminology and taxonomy.
Definition of CPP
Chronic pelvic pain is chronic or persistent pain perceived* in
structures related to the pelvis of either men or women. It is
often associated with negative cognitive, behavioural, sexual
and emotional consequences as well as with symptoms
suggestive of lower urinary tract, sexual, bowel, pelvic floor or
gynaecological dysfunction.
(*Perceived indicates that the patient and clinician, to the
best of their ability from the history, examination and
investigations (where appropriate) have localised the pain
as being perceived in the specified anatomical pelvic area.)
Definition of CPPS
Chronic pelvic pain syndrome (CPPS) is the occurrence of
CPP when there is no proven infection or other obvious local
pathology that may account for the pain. It is often associated
with negative cognitive, behavioural, sexual or emotional
consequences, as well as with symptoms suggestive of lower
urinary tract, sexual, bowel or gynaecological dysfunction.
CPPS is a subdivision of CPP.

Table 2: Chronic Pelvic Pain Syndromes
Urological Pain Syndromes

Prostate pain Prostate pain syndrome is the occurrence of persistent
syndrome (PPS) or recurrent episodic pain (which is con-vincingly
reproduced by prostate palpation). There is no
proven infection or other obvious local pathology.
Prostate pain syndrome is often associated with
negative cognitive, behavioural, sexual or emotional
consequences, as well as with symptoms suggestive
of lower urinary tract and sexual dysfunction. The term
“chronic prostatitis” continues to be equated with that
of PPS. In the authors’ and others’ opinion, this is an
inappropriate term, although it is recognised that it has
a long history of use. The National Institutes of Health
(NIH) consensus includes infection (types I and II),
which the authors feel should not be considered under
PPS, but as specific disease-associated pelvic pain. The
term prostadynia has also been used in the past but is
no longer recommended by the panel. Please note that
some of the authors of the International Association
for the Study of Pain document disagree with this term
and suggest that CPPS of the male is used instead of
PPS, which has been agreed by the majority.

Bladder pain Bladder pain syndrome is the occurrence of persistent
syndrome (BPS) or recurrent pain perceived in the urinary bladder
region, accompanied by at least one other symptom,
such as pain worsening with bladder filling and day-
time and/or night-time urinary frequency. There is
no proven infection or other obvious local pathology.
Bladder pain syndrome is often associated with
of lower urinary tract and sexual dysfunction. Bladder
pain syndrome is believed to represent a
heterogeneous spectrum of disorders. There may be
specific types of inflammation as a feature in subsets
of patients. Localisation of the pain can be difficult
by examination, and consequently, another localising
symptom is required. Cystoscopy with hydrodistension
and biopsy may be indicated to define phenotypes.
Recently, the International Society for the Study of
BPS has suggested a standardised scheme of
subclassifications to acknowledge differences and
make it easier to compare various studies. Other terms
that have been used include “interstitial cystitis” (IC),
“painful bladder syndrome” (PBS), and “PBS/IC” or
“BPS/IC”. These terms are no longer recommended.
Scrotal pain Scrotal pain syndrome is the occurrence of persistent
syndrome or recurrent episodic pain localised within the organs
of the scrotum, and may be associated with symptoms
suggestive of lower urinary tract or sexual dysfunction.
There is no proven infection or other obvious local
pathology. Scrotal pain syndrome is often associated
with negative cognitive, behavioural, sexual or
emotional consequences. Scrotal pain syndrome is a
generic term and is used when the site of the pain is
not clearly testicular or epididymal. The pain is not in
the skin of the scrotum as such, but perceived within
its contents, in a similar way to idiopathic chest pain.

Testicular pain Testicular pain syndrome is the occurrence of
syndrome persistent or recurrent episodic pain perceived in
the testes, and may be associated with symptoms
pathology. Testicular pain syndrome is often associated
with negative cognitive, behavioural, sexual or
emotional consequences. Previous terms have
included orchitis, orchialgia and orchiodynia. These
terms are no longer recommended.
Epididymal pain Epididymal pain syndrome is the occurrence of
syndrome persistent or recurrent episodic pain perceived in the
epididymis, and may be associated with symptoms
pathology. Epididymal pain syndrome is often
associated with negative cognitive, behavioural, sexual
or emotional consequences.
Penile pain Penile pain syndrome is the occurrence of pain within
syndrome the penis that is not primarily in the urethra, in the
absence of proven infection or other obvious local
pathology. Penile pain syndrome is often associated
consequences, as well as with symptoms suggestive of
lower urinary tract and sexual dysfunction.
Urethral pain Urethral pain syndrome is the occurrence of chronic
syndrome or recurrent episodic pain perceived in the urethra, in
the absence of proven infection or other obvious local
pathology. Urethral pain syndrome is often associated
of lower urinary tract, sexual, bowel or gynaecological
dysfunction. Urethral pain syndrome may occur in men
and women.

Post-vasectomy Post-vasectomy scrotal pain syndrome is a scrotal pain
scrotal pain syndrome that follows vasectomy. Post-vasectomy
syndrome scrotal pain syndrome is often associated with
of lower urinary tract and sexual dysfunction. Post-
vasectomy pain may be as frequent as 1% following
vasectomy, possibly more frequent. The mechanisms
are poorly understood and for that reason it is
considered a special form of scrotal pain syndrome.
Gynaecological Pain Syndromes: external genitalia
Vulvar pain Vulvar pain syndrome is the occurrence of persistent
syndrome or recurrent episodic vulvar pain. There is no proven
infection or other local obvious pathology. It is often
or emotional consequences, as well as with symptoms
suggestive of lower urinary tract, sexual, bowel or
gynaecological dysfunction. Although pain perceived
in the vulva was included under sexual disorders in
the The Diagnostic and Statistical Manual of Mental
Disorders (DSM-IV-R) for classifying psychiatric
disorders, there is no scientific basis for this
classification, and pain perceived in the vulva is best
understood as a pain problem that usually has
psychological consequences. There is no evidence
for its classification as a psychia-tric disorder. The
International Society for the Study of Vulvovaginal
Disease (ISSVD) has used the term vulvodynia, where
we use the term vulvar pain syndrome. According
to the ISSVD, vulvodynia is vulvar pain that is not
accounted for by any physical findings. The ISSVD has
defined vulvodynia as “vulvar discomfort, most often
described as burning pain, occurring in the absence
of relevant visible findings or a specific, clinically
identifiable, neurologic disorder”. If physical findings
are present, the patient is said to have vulvar pain due
to a specified cause. The ISSVD has subdivided
vulvodynia based on pain location and temporal
characteristics of the pain (e.g. provoked or
unprovoked). The following definitions are based on
that approach.

Generalised Generalised vulvar pain syndrome refers to a vulvar
vulvar pain pain syndrome in which the pain/burning cannot be
syndrome consistently and precisely localised by point-pressure
mapping via probing with a cotton-tipped applicator
or similar instrument. Rather, the pain is diffuse and
affects all parts of the vulva. The vulvar vestibule (the
part that lies between the labia minora into which
the urethral meatus and vaginal introitus open) may
be involved but the discomfort is not limited to the
vestibule. This pain syndrome is often associated with
consequences. Previous terms have included
“dysesthetic vulvodynia” and “essential vulvodynia”,
but are no longer recommended.
Localised vulvar Localised vulvar pain syndrome refers to pain that
pain syndrome can be consistently and precisely localised by point-
pressure mapping to one or more portions of the vulva.
Clinically, the pain usually occurs as a result of provo-
cation (touch, pressure or friction). Localised vulvar
pain syndrome can be sub-divided into vestibular pain
syndrome and clitoral pain syndrome.
Vestibular pain Vestibular pain syndrome refers to pain that can be
syndrome localised by point-pressure mapping to the vestibule or
is well perceived in the area of the vestibule.
Clitoral pain Clitoral pain syndrome refers to pain that can be
syndrome localised by point-pressure mapping to the clitoris or
is well-perceived in the area of the clitoris.

Gynaecological Pain Syndromes: internal pelvic pain syndromes
Endometriosis- Endometriosis-associated pain syndrome is chronic or
associated recurrent pelvic pain in patients with laparoscopically
pain syndrome confirmed endometriosis, and the term is used when
the symptoms persist despite adequate endometriosis
treatment. It is often associated with negative
cognitive, behavioural, sexual or emotional
of lower urinary tract, sexual, bowel or gynaecological
dysfunction. Many patients have pain above and
beyond the endometriotic lesions; this term is used to
cover that group of patients. Endometriosis may be an
incidental finding, is not always painful, and the degree
of disease seen laparoscopically does not correlate
with severity of symptoms. As with other patients,
they often have more than one end-organ involved.
It has been suggested that this phenotype should be
removed from the classification because the
endometriosis may be irrelevant.
Chronic pelvic Chronic pelvic pain syndrome with cyclical
pain syndrome exacerbations covers the non-gynaecological organ
with cyclical pain that frequently shows cyclical exacerbations
exacerbations (e.g., Irritable bowel syndrome (IBS) or BPS) as well as
pain similar to that associated with endometriosis/
adenomyosis but where no pathology is identified. This
condition is different from dysmenorrhoea, in which
pain is only present with menstruation.
Dysmenorrhoea Dysmenorrhoea is pain with menstruation that
is not associated with well-defined pathology.
Dysmenorrhoea needs to be considered as a chronic
pain syndrome if it is persistent and associated with
consequences.

Gastrointestinal Pelvic Pain Syndromes
Irritable bowel Irritable bowel syndrome is the occurrence of chronic
syndrome or recurrent episodic pain perceived in the bowel, in
the absence of proven infection or other obvious local
pathology. Bowel dysfunction is frequent. Irritable
bowel syndrome is often associated with worry and
pre-occupation about bowel function, and negative
cognitive, behavioural, sexual or emotional
consequences, as well as with symptoms suggestive of
lower urinary tract or gynaecological dysfunction. The
above classification is based upon the Rome III Criteria:
three months of continuous or recurring symptoms of
abdominal pain or irritation that may be relieved with a
bowel movement, may be coupled with a change in
frequency, or may be related to a change in stool
consistency. Two or more of the following are present
at least 25% of the time: change in stool frequency
(more than three bowel movements per day or less
than three per week); noticeable difference in stool
form (hard, loose, watery or poorly formed stools);
passage of mucus in stools; bloating or feeling of
abdominal distension; or altered stool passage (e.g.,
sensation of incomplete evacuation, straining, or
urgency). Extra-intestinal symptoms include: nausea,
fatigue, full sensation after even a small meal and
vomiting.
Chronic anal Chronic anal pain syndrome is the occurrence of
pain syndrome chronic or recurrent episodic pain perceived in the
anus, in the absence of proven infection or other
obvious local pathology. Chronic anal pain syndrome is
often associated with negative cognitive, behavioural,
sexual or emotional consequences, as well as with
symptoms suggestive of lower urinary tract, sexual,
bowel or gynaecological dysfunction.
Intermittent Intermittent chronic anal pain syndrome refers to
chronic anal severe, brief, episodic pain that seems to arise in the
pain syndrome rectum or anal canal and occurs at irregular intervals.
This is unrelated to the need to or the process of
defecation. It may be considered a subgroup of the
chronic anal pain syndromes. It was previously known
as “proctalgia fugax” but this term is no longer
recommended.

Musculoskeletal System
Pelvic floor Pelvic floor muscle pain syndrome is the occurrence of
muscle pain persistent or recurrent episodic pelvic floor pain. There
syndrome is no proven well-defined local pathology. It is often
gynaecological dysfunction. This syndrome may be
associated with over-activity of or trigger points within
the pelvic floor muscles. Trigger points may also be
found in several muscles, such as the abdominal, thigh
and paraspinal muscles and even those not directly
related to the pelvis.
Coccyx pain Coccyx pain syndrome is the occurrence of chronic or
syndrome recurrent episodic pain perceived in the region of the
coccyx, in the absence of proven infection or other
obvious local pathology. Coccyx pain syndrome is often
gynaecological dysfunction. The term “coccydynia” was
used but is no longer recommended.

Epidemiology, Aetiology and Pathophysiology
Chronic visceral pain, pelvic pain and abdominal aspects of
pelvic pain

All of those involved in the management Strong
of Chronic Pelvic Pain (CPP) should have
knowledge of peripheral and central pain
mechanisms.
The early assessment of patients with CPP Strong
should involve investigations aimed at
specific disease-associated pelvic pain.
The early assessment of patients with CPP Strong
should involve assessment of functional,
emotional, behavioural, sexual and other
quality of life issues, such as effect on work
and socialisation.
Manage Chronic Pelvic Pain Syndrome Strong
patients in a multispecialty and
multidisciplinary environment with
consideration of all their symptoms.
History and physical examination
History is very important for the evaluation of patients with
CPP. Pain syndromes are symptomatic diagnoses which are
derived from a history of pain perceived in the region of the
pelvis, and absence of other pathology, for a minimum of
three out of the past six months. This implies that specific
disease-associated pelvic pain caused by bacterial infection,
cancer, primary anatomical or functional disease of the pelvic
organs, and neurogenic disease must be ruled out. The history
should be comprehensive covering functional as well as pain
related symptoms. The clinical examination often serves to

confirm or refute the initial impressions gained from a good
history. The examination should be aimed at specific
questions where the outcome of the examination may change
management. As well as a local examination, a general
musculoskeletal and neurological examination should be
considered an integral part of the assessment and be
undertaken, if appropriate.
Figure 1: Diagnosing chronic pelvic pain
Chronic Pelvic Pain
Physical
History
examination
Specific disease
associated
yes with pelvic pain
Symptom of a well
known disease
no
Pelvic pain
syndrome
Organ specific
symptoms present
yes
Urology Gynaecology Gastro- Neurology Sexology Pelvic

enterology floor
Phenotype and proceed according to Chronic Pelvic Pain Guideline.

Figure 2: Phenotyping of pelvic pain
Phenotyping Assessment
Urology Urinary flow, micturition diary, cystoscopy, ultrasound, uroflowmetry
Psychology Anxiety about pain, depression and loss of function, history of negative sexual experiences
Ask for gynaecological, gastro-intestinal, ano-rectal, sexological complaints

Organ specific
Gynaecological examination, rectal examination
Infection Semen culture and urine culture, vaginal swab, stool culture
Ask for neurological complaints (sensory loss, dysaesthesia).

Neurological
Neurological testing during physical examination: sensory problems, sacral reflexes and muscular function.
Tender muscle Palpation of the pelvic floor muscles, the abdominal muscles and the gluteal muscles
Sexological Erectile function, ejaculatory function, post-orgasmic pain
Recommendations for diagnostic evaluation

evaluation of Prostate Pain Syndrome
Adapt diagnostic procedures to the patient. Strong
Exclude specific diseases with similar
symptoms.
Use a validated symptom and quality of life Strong
scoring instrument, such as the National
Institutes of Health Chronic Prostatitis
Symptom Index, for initial assessment and
follow-up.
Assess prostate pain syndrome associated Strong
negative cognitive, behavioural, sexual,
or emotional consequences, as well as
symptoms of lower urinary tract and sexual
dysfunctions.

evaluation of Bladder Pain Syndrome
Perform general anaesthetic rigid cysto- Strong
scopy in patients with bladder pain to
subtype and rule out confusable disease.
Diagnose patients with symptoms Strong
according to the EAU definition, after
primary exclusion of specific diseases,
with bladder pain syndrome (BPS) by
subtype and phenotype.
Assess BPS associated non-bladder Strong
diseases systematically.
Assess BPS associated negative cognitive, Strong
behavioural, sexual, or emotional conse-
quences.
Use a validated symptom and quality of life Strong
scoring instrument for initial assessment
and follow-up.

evaluation of gynaecological aspects of CPP
Take a full gynaecological history and Strong
evaluate to rule out a treatable cause (e.g.
endometriosis) in all women with chronic
pelvic pain.
Refer to a gynaecologist if clinical Strong
suspicion of a gynaecological cause for
pain following complete urological
evaluation. Laparoscopy should be
undertaken in accordance with
gynaecological guidelines.

Recommendation for the diagnostic Strength rating
evaluation of Anorectal Pain Syndrome
Anorectal function tests are recommended Strong
in patients with anorectal pain.

evaluation of Pudendal Neuralgia
Rule out confusable diseases, such as Strong
neoplastic disease, infection, trauma and
spinal pathology.
If a peripheral nerve pain syndrome is Weak
suspected, refer early to an expert in the
field, working within a multi-disciplinary
team environment.
Imaging and neurophysiology help Weak
diagnosis but image and nerve locator
guided local anaesthetic injection is
preferable.
Recommendation for the diagnostic Strength rating

evaluation of sexological aspects in CPP
Screen patients presenting with symptoms Weak
suggestive for chronic pelvic pain syndrome
for abuse, without suggesting a causal
relation with the pain.

evaluation of psychological aspects of CPP
Assess patient psychological distress in Strong
relation to their pain.
Ask patients what they think is the cause Strong
of their pain to allow the opportunity to
inform and reassure.

evaluation of pelvic floor function
Use ICS classification for pelvic floor Strong
muscle function and dysfunction.
Actively look for the presence of myofascial Weak
trigger points in patients with chronic
pelvic pain syndrome.
Management
The philosophy for the management of CPP is based on a
bio-psychosocial model. This is a holistic approach with the
patients’ active involvement. Single interventions rarely work
in isolation and need to be considered within a broader
personalised management strategy. The management strategy
may well have elements of self-management. Pharmacological
and non-pharmacological interventions should be considered
with a clear understanding of the potential outcomes and end
points. These may include: psychology, physiotherapy, drugs
and more invasive interventions. Providing information that
is personalised and responsive to the patient’s problems,
conveying belief and concern, is a powerful way to allay
anxiety. Additional written information or direction to
reliable sources is useful; practitioners tend to rely on locally
produced material or pharmaceutical products of variable
quality while endorsing the need for independent materials for
patients.

Recommendations for the management of Strength rating
Prostate Pain Syndrome
Offer multimodal and phenotypically Weak
directed treatment options for Prostate
Pain Syndrome (PPS).
Use antimicrobial therapy (quinolones or Strong
tetracyclines) over a minimum of six weeks
in treatment-naïve patients with a duration
of PPS less than one year.
Use α-blockers for patients with a duration Strong
of PPS less than one year.
Offer high-dose oral pentosane Weak
polysulphate in PPS.
Offer acupuncture for use in PPS. Strong
Offer non-steroidal anti-inflammatory drugs Weak
in PPS, but long-term side-effects have to
be considered.

Bladder Pain Syndrome
Offer subtype and phenotype-oriented Strong
therapy for the treatment of Bladder Pain
Syndrome (BPS).
Always consider offering multimodal Strong
behavioural, physical and psychological
techniques alongside oral or invasive
treatments of BPS.
Administer amitriptyline for treatment of Strong
BPS.
Offer oral pentosane polysulphate for the Strong
treatment of BPS.

Offer oral pentosane polysulphate plus Weak
subcutaneous heparin in low responders
to pentosane polysulphate alone.
Administer intravesical lidocaine plus Weak
sodium bicarbonate prior to more invasive
methods.
Administer intravesical pentosane poly- Strong
sulphate before more invasive treatment
alone or combined with oral pentosane
polysulphate.
Administer submucosal injection of Strong
Botulinum toxin type A (BTX-A) plus
hydrodistension if intravesical instillation
therapies have failed.
Only undertake ablative organ surgery as Strong
the last resort and only by experienced and
BPS-knowledgeable surgeons.
Offer intravesical hyaluronic acid before Weak
more invasive measures.
Offer intravesical chondroitin sulphate Weak
before more invasive measures.
Offer transurethral resection (or coagula- Strong
tion or laser) of bladder lesions, but in BPS
type 3 C only.
Offer neuromodulation before more Weak
invasive interventions.
Offer dietary advice. Weak
Offer intravesical heparin before more Weak
invasive measures alone or in combination
treatment.
Offer intravesical bladder wall and trigonal Strong
injection of BTX-A if intravesical instillation
therapies have failed.

Do not recommend corticosteroids for Strong
long-term treatment.
Do not use bladder distension as a Weak
treatment of BPS.

Scrotal Pain Syndrome
Inform about the risk of post-vasectomy Strong
pain when counselling patients planned for
vasectomy.
Do open instead of laparoscopic inguinal Strong
hernia repair, to reduce the risk of scrotal
pain.
In patients with testicular pain improving Weak
after spermatic block, offer microsurgical
denervation of the spermatic cord.

gynaecological aspects of CPP
Involve a gynaecologist to provide Strong
therapeutic options such as hormonal
therapy or surgery in well-defined disease
states.
Provide a multidisciplinary approach to Strong
pain management in persistent disease
states.
Recommendations for functional anorectal Strength rating

pain
Undertake biofeedback treatment in Strong
patients with chronic anal pain.

Offer Botulinum toxin type A and electro- Strong
galvanic stimulation in chronic anal pain
syndrome.
Offer percutaneous tibial nerve stimulation Weak
in chronic anal pain syndrome.
Offer sacral neuromodulation in chronic Weak
anal pain syndrome.
Offer inhaled salbutamol in intermittent Weak
chronic anal pain syndrome.
Recommendation for the management of Strength rating

pudendal neuralgia
Neuropathic pain guidelines are well- Strong
established. Use standard approaches to
management of neuropathic pain.

sexological aspects in CPP
Offer behavioural strategies to the patient Weak
and his/her partner to reduce sexual
dysfunctions.
Offer pelvic floor muscle therapy as part of Weak
the treatment plan to improve quality of life
and sexual function.
Recommendation for the management of Strength rating

psychological aspects in CPP
For CPP with significant psychological Strong
distress, refer patient for CPP-focused
psychological treatment.

pelvic floor dysfunction
Apply myofascial treatment as first line Weak
treatment.
Offer biofeedback as therapy adjuvant to Strong
muscle exercises, in patients with anal pain
due to an overactive pelvic floor.
Recommendations for the management Strength rating

of chronic/non-acute urogenital pain by
opioids
Prescribe opioid treatment, following Strong
multidisciplinary assessment and only
after other reasonable treatments have
been tried and failed.
The decision to instigate long-term opioid Strong
therapy should be made by an
appropriately trained specialist in
consultation with the patient and their
family doctor.
Where there is a history or suspicion of Strong
drug abuse, involve a psychiatrist or
psychologist with an interest in pain
management and drug addiction.
This short booklet is based on the more comprehensive EAU

Guidelines (ISBN 978-94-92671-01-1), available to all members of the

EAU GUIDELINES ON
RENAL TRANSPLANTATION
A. Breda (Chair), K. Budde, A. Figueiredo, E. Lledó García,

J. Olsburgh (Vice-chair), H. Regele.
Guidelines Associates: R. Boissier, C. Fraser Taylor, V. Hevia,
O. Rodríguez Faba, R.H. Zakri.
Introduction
The European Association of Urology (EAU) Renal
Transplantation Guidelines aim to provide a comprehensive
overview of the medical and technical aspects relating to
renal transplantation.
Organ retrieval and transplantation surgery
Living-donor nephrectomy

Offer pure or hand-assisted laparoscopic/ Strong
retroperitoneoscopic surgery as the
preferential technique for living-donor
nephrectomy.
Perform open living-donor nephrectomy in Strong
centres where endoscopic techniques are
not implemented.
Perform laparo-endoscopic single site Strong
surgery, robotic and natural orifice trans-
luminal endoscopic surgery-assisted living-
donor nephrectomy in highly-specialised
centres only.
378 Renal Transplantation

Organ preservation
Recommendations for kidney storage Strength rating

solutions
Use either University of Wisconsin or Strong
histidine tryptophane ketoglutarate
preservation solutions for cold storage.
Use Celsior or Soltran solution for cold Strong
storage if University of Wisconsin or
histidine tryptophane ketoglutarate
solutions are not available.
Recommendations for kidney preservation: Strength rating

static and dynamic preservation
Use cold and warm ischemia time as Strong
predictors of delayed graft function.
Use hypothermic machine-perfusion in Strong
type III kidneys from donors after cardiac
death, kidneys with prolonged simple cold
storage and expanded criteria donor
kidneys.
Hypothermic machine-perfusion may be Strong
used in standard criteria deceased donor
kidneys.
Use low pressure values in hypothermic Strong
machine perfusion preservation.
Hypothermic machine-perfusion must be Strong
continuous and controlled by pressure and
not flow.
Do not discard grafts due to only increased Weak
vascular resistance and high perfusate
injury marker concentrations during hypo-
thermic machine perfusion preservation.
Renal Transplantation 379

Donor kidney biopsies

Do not base decisions on the acceptance Strong
of a donor organ on histological findings
alone, since this might lead to an unneces-
sary high rate of discarded grafts. Interpret
histology in context with clinical para-
meters of donor and recipient including
perfusion parameters where available.
Use paraffin histology for histomorphology Strong
as it is superior to frozen sections, however,
its diagnostic value has to be balanced
against a potential delay of transplantation.
Submit 14 or 16 G needle core biopsies, Weak
wedge biopsies or skin punch biopsies for
histopathology.
Procurement biopsies should be read by a Strong
renal pathologist or a general pathologist
with specific training in kidney pathology.
Living and deceased donor implantation surgery

Immediate pre-op haemodialysis
Use dialysis or conservative measures to Weak
manage fluid and electrolyte imbalance
prior to transplant surgery taking into
consideration the likelihood of immediate
graft function.

Operating on patients taking anti-platelet and anti-
coagulation agents
Consider continuing anti-platelet therapy Weak
in patients on the transplant waiting list.
Discuss patients who take anti-platelet and Weak
anti-coagulation agents prior to transplant
surgery with relevant cardiologist /
haematologist /nephrologist.
Prevention of venous thrombosis including deep vein
thrombosis during and after renal transplant
Do not routinely give post-operative Weak
prophylactic unfractionated or low-
molecular-weight heparin to low-risk living
donor transplant recipients.
Peri-operative antibiotics in renal transplant
Use single-dose, rather than multi-dose, Strong
peri-operative prophylactic antibiotics in
routine renal transplant recipients.
Specific fluid regimes during renal transplantation
Optimise pre-, peri- and post-operative Strong
hydration to improve renal graft function.
Use balanced crystalloid solutions for intra- Weak
operative intravenous fluid therapy.
Use target directed intra-operative hydra- Strong
tion to decrease delayed graft function
rates and optimise early graft function.
Dopaminergic drugs in renal transplantation
Do not routinely use low-dose Weak
dopaminergic agents in the early
post-operative period.

Surgical approaches for first, second, third and further
transplants
Single kidney transplant – living and deceased donors

Assess the utility (including inspection) Strong
of the kidney for transplantation before
commencement of immunosuppression
and induction of anaesthesia for deceased
donor kidney transplantation.
Choose either iliac fossa for placement of Weak
a first or second single kidney transplant.
Ligate peri-iliac vessel lymphatics Weak
(lymphostasis) to reduce post-operative
lymphocele.
Assess the length of the donor renal vein Weak
and if it is short consider one of a variety of
surgical techniques to optimise the venous
anastomosis.
Use the external or common iliac arteries Weak
for an end-to-side arterial anastomosis to
donor renal artery.
Use an end-to-end anastomosis to the Weak
internal iliac artery as an alternative to
external or common iliac arteries.
Check the intima of the donor and Strong
recipient arteries prior to commencing the
arterial anastomosis to ensure that there
is no intimal rupture/flap. If this is found
it must be repaired prior to/as part of the
arterial anastomosis.

Pre-operatively plan the surgical approach Strong
in third or further transplants, to ensure
that appropriate arterial inflow and venous
outflow exists with adequate space to
implant the new kidney.
Emerging surgical technologies

Robot-assisted kidney transplant (RAKT) surgery is being
evaluated in prospective non-randomised trials (using IDEAL
consortium principles). Whilst potential advantages may
exist (decreased post-operative pain, length of hospital
stay, incision length and lymphocele rate), evidence is too
premature to recommend RAKT.
Dual kidney transplants

Dual kidney transplant is performed when the quality of a
single deceased donor kidney is thought to be insufficient
for appropriate long-term graft function and that the outcome
with both kidneys would be better. A variety of surgical tech-
niques have been described to implant a pair of donor kidneys
these include: unilateral extra-peritoneal or intra-peritoneal
and bilateral extra-peritoneal or intra-peritoneal that can
be via a midline or two lateral incisions. No randomised
controlled trials exist to recommend one technique for all
patients or situations.
Ureteric implantation in normal urinary tract

Ureteric anastomotic techniques described for renal trans-
plant recipients with no underlying urological abnormality
include: extra (Lich-Gregoir) or intra (Ledbetter-Politano)
vesical uretero-neo-cystotomy and uretero-ureterostomy
using native ureter.

Perform Lich-Gregoir-like extra-vesical Strong
ureteric anastomosis technique to
minimise urinary tract complications in
renal transplant recipients with normal
urological anatomy.
Pyelo/uretero-ureteral anastomosis is an Strong
alternative especially for a very short or
poorly vascularised transplant ureter.
Transplantation/ureteric implantation in abnormal urogenital

tract
The following points should be considered when performing
kidney transplantation in the abnormal urogenital tract:
• In patients with an ileal conduit, a kidney transplant may be
placed upside down to align the ureter to the conduit and
avoid a redundant ureter.
• The technique used to implant transplant ureter(s) into an
ileal conduit is the same as the method used with native
ureter(s) (Bricker; Wallace).
• In bladder augmentation or continent pouches, ureters
should be implanted with a tunnel technique or extra-
vesically (Lich-Gregoir). The latter is favoured in most
patients.
• In patients with a Mitrofanoff catheterisable stoma or
continent ileo-caecal pouch with catheterisable stoma,
consideration should be given to the positioning of the
catheterisable stoma (umbilical or iliac fossa - usually
right-side) with clear communication with the transplant
surgeons so that the position of any future transplant
kidney is not compromised. If an intraperitoneal placement
of a future kidney transplant is likely, then placement of
a Mitrofanoff exiting in the iliac fossa is preferable at the
umbilicus. If a future kidney transplant is likely in the right

iliac fossa then placement of a Mitrofanoff exiting at the
umbilicus or left iliac fossa may be preferable.
Donor complications
Living-donor nephrectomy, like any other intervention, is
potentially associated with complications and mortality.
However, the fact that the operation is performed on a healthy
individual amplifies the relevance of any complications. Intra-
operative complications occur in 2.2% (the most common
being bleeding in 1.5% and injury to other organs in 0.8%)
and post-operative complications occur in 7% ( infectious
complications in 2.6% and bleeding in 1%). Potential
complications should be included in the process of informed
consent. Long term complications are mostly related to the
single-kidney condition. Health related quality of life, including
mental condition, remains on average better than the general
population after donation.

Restrict living donor nephrectomy to Strong
specialised centres.
Offer long-term follow-up to all living kidney Strong
donors.
Recipient complications
Surgical complications during and after kidney transplantation
may expose the recipient to an increased risk of morbidity
and mortality. The incidence and management of such
complications is therefore of primary importance. The most
common surgical complications in renal transplantation are
summarised below.
Haemorrhage
The incidence of haematomas is reported to be between
0.2-25%. Small and asymptomatic hematomas do not usually

require any intervention. In case of larger hematomas,
clinical signs and symptoms due to external pressure
with graft dysfunction and/or thrombotic graft vessels
complications can be present. These cases may be treated by
percutaneous drainage under computed tomography or
ultrasound guidance or may require surgical treatment.
Arterial thrombosis
Transplant renal artery thrombosis is a rare complication
(prevalence 0.5-3.5%).

Perform ultrasound-colour-doppler in case Strong
of suspected graft thrombosis.
Perform surgical exploration in case of Strong
ultrasound finding of poor graft perfusion.
Perform a surgical thrombectomy in case of Weak
a salvageable graft if arterial thrombosis is
confirmed intra-operatively.
Perform an allograft nephrectomy in case Strong
of a non-viable graft.
Venous thrombosis
Transplant renal vein thrombosis is an early complication
(prevalence 0.5-4%) and one of the most important causes of
graft loss during the first post-operative month.

Perform ultrasound-colour-doppler in case Strong
of suspected graft thrombosis.
Perform surgical exploration in case of Weak
ultrasound finding of poor graft perfusion.

If venous thrombosis is confirmed Weak
intra-operatively, perform a surgical
thrombectomy in case of a salvageable
graft or an allograft nephrectomy in case
of a non-viable graft.
Do not routinely use pharmacologic Strong
prophylaxis to prevent transplant renal vein
thrombosis.
Transplant renal artery stenosis

The incidence of transplant renal artery stenosis is 1-25%.
Risk factors include small calibre and atherosclerosis of the
donor artery, trauma to donor artery at procurement, absence
of arterial patch, suturing technique (interrupted versus
continuous), and damage to the iliac artery during
transplantation.

Perform ultrasound-colour-doppler to Strong
diagnose an arterial stenosis, in case of
undetermined results on ultrasound con-
sider a magnetic resonance or computed
tomography angiogram.
Perform percutaneous transluminal Strong
angioplasty/stent, if feasible, as first-line
treatment for an arterial stenosis.
Offer surgical treatment in case of recent Strong
transplant, multiple, long and narrow
stenosis, or after failure of angioplasty.
Arteriovenous fistulae and pseudo-aneurysms after renal

biopsy
Percutaneous biopsy may result in arteriovenous fistulae
and/or intrarenal pseudo-aneurysms in 1-18% of cases.

Perform a ultrasound-colour-doppler if a Strong
arteriovenous fistulae or pseudo-aneurysm
is suspected.
Perform angiographic embolisation as first- Strong
line treatment in symptomatic cases of
arteriovenous fistulae or pseudo-aneurysm.
Lymphocele
Lymphocele is a relatively common complication (prevalence
1-26%). There is a significant aetiological association with
diabetes, m-TOR inhibitors (i.e sirolimus) therapy, and acute
rejection.

Perform percutaneous drainage placement Strong
as the first treatment for large and
symptomatic lymphocele.
Perform fenestration when percutaneous Strong
treatments fail.
Urinary leak
Urinary leakage occurs in 0-9.3% of cases.

Manage urine leak by JJ-stent and Strong
bladder catheter and/or percutaneous
nephrostomy tube.
Perform surgical repair in cases of failure of Strong
conservative management.
Ureteral stenosis
Ureteral stenosis is a common complication in recipients, with
an incidence of 0.6-10.5%. Early stenosis (within three months

of surgery) is usually caused by surgical technique or
compromised ureteral blood supply during surgery. Late
stenosis (after six months) is provoked by infection, fibrosis,
progressive vascular disease and/or rejection.

In case of ureteral stricture, place a Strong
nephrostomy tube for both kidney
decompression and stricture diagnosis via
an antegrade pyelogram.
Manage strictures < 3 cm in length either Strong
with surgical reconstruction or endo-
scopically (percutaneous balloon dilation
or antegrade flexible ureteroscopy and
holmium laser incision).
Treat late stricture recurrence and/or Strong
stricture > 3 cm in length with surgical
reconstruction in appropriate recipients.
Haematuria
The incidence of haematuria ranges from 1-34%. The
Lich-Gregoire technique provides the lowest incidence of
haematuria. Bladder irrigation is the first line of treatment.
Some cases require cystoscopy with evacuation of clots
and/or fulguration of bleeding sites.
Reflux and acute pyelonephritis

The frequency of vesicoureteral reflux is between 1-86%. Acute
graft pyelonephritis occurs in 13% of graft recipients. Patients
with lower tract urinary infections and cytomegalovirus (CMV)
infection present a higher risk of acute graft pyelonephritis.

Use an endoscopic approach as first-line Weak
treatment for symptomatic reflux.
Kidney stones
Urolithiasis occurs in 0.2-1.7% of recipients.

Evaluate the causes of urolithiasis in the Strong
recipient.
Treat ureteral obstruction due to a stone Strong
with a percutaneous nephrostomy tube or
JJ-stent placement.
Perform shockwave lithotripsy or Strong
antegrade/retrograde ureteroscopy for
stones < 15 mm.
Perform percutaneous nephrolithotomy for Weak
stones > 20 mm.
Wound infection
Wound infections occur in about 4% of cases. Subcutaneous
sutures, pre-dialysis transplantation, sealing or ligation of
lymphatic trunks, prophylactic fenestration, reducing
corticosteroid load, and avoiding sirolimus/everolimus therapy
can decrease wound complication rates.
Incisional hernia
Incisional hernia occurs in approximately 4% of open kidney
transplantations. Mesh infection is a risk factor for incisional
hernia recurrence. Open and laparoscopic repair approaches
are safe and effective.

Matching of donors and recipients
Histocompatibility antigens show remarkable polymorphism
and human leukocyte antigen (HLA) matching is still very
important in kidney transplantation as transplant outcome
correlates with the number of HLA mismatches.

Determine the ABO blood group and the Strong
human leukocyte antigen A, B, C and DR
phenotypes for all candidates awaiting
kidney transplantation.
Test both the donor and recipient for Strong
human leukocyte antigen DQ. Human
leukocyte antigen DP testing may be
performed for sensitised patients.
Perform thorough testing for HLA Strong
antibodies before transplantation.
Perform adequate cross-match tests to Strong
avoid hyper-acute rejection, before each
kidney and combined kidney/pancreas
transplantation.
Immunosuppression after kidney transplantation

The principle underlying successful immunosuppression is
‘the balance of survival’. Practitioners must prescribe a
dosage of drug high enough to suppress rejection without
endangering the recipient’s health.
The currently recommended standard initial immunosuppres-

sion regime provides excellent efficacy with good tolerability.
It is given to most patients and consists of:
• calcineurin inhibitors (preferably tacrolimus, alternatively
cyclosporine);

• mycophenolate (MMF or enteric-coated mycophenolate
sodium;
• steroids (prednisolone or methylprednisolone);
• induction therapy (preferably basiliximab in low and
standard risk patients and anti-thymocyte globulin (ATG)
in high risk patients).

General immunosuppression after kidney transplantation
Perform initial rejection prophylaxis with a Strong
combination therapy of a calcineurin inhibi-
tor (preferably tacrolimus), mycophenolate,
steroids and an induction agent (either
basiliximab or anti-thymocyte globulin).
Calcineurin inhibitors
Use calcineurin inhibitors for rejection Strong
prophylaxis as they represent current best
practice pending publication of long-term
results using newer agents.
Use tacrolimus as first-line calcineurin Strong
inhibitor due to its higher efficacy.
Monitor blood-levels of both cyclosporine Strong
and tacrolimus to allow appropriate dose
adjustment of calcineurin inhibitors.
Mycophenolates (MPA)
Administer mycophenolate as part of the Strong
initial immunosuppressive regimen.
Azathioprine
Azathioprine may be used in a low-risk Weak
population as an immunosuppressive
drug, especially for those intolerant to
mycophenolate formulations.

Steroids
Initial steroid therapy should be part of Strong
immunosuppression in the peri-operative
and early post-transplant period.
Consider steroid withdrawal in standard Weak
immunological risk patients on combina-
tion therapy with calcineurin inhibitors
and mycophenolic acid after the early
post-transplant period.
Inhibitors of the mammalian target of rapamycin (m-TOR)
The m-TOR inhibitors may be used to Weak
prevent rejection in patients who are
intolerant to standard therapy.
Significantly reduce calcineurin inhibitor Strong
dosage in a combination regimen with
m-TOR inhibitors to prevent aggravated
nephrotoxicity.
Do not convert patients with proteinuria Strong
and poor renal function to m-TOR
inhibitors.
Monitor blood-levels of both sirolimus and Strong
everolimus to allow for appropriate dose
adjustment.
Induction with Interleukin-2 receptor antibodies
Use interleukin-2 receptor antibodies for Weak
induction in patients with normal immuno-
logical risk in order to reduce incidence of
acute rejection.
T-cell depleting induction therapy
T-cell depleting antibodies may be used for Weak
induction therapy in immunologically high
risk patients.

Belatacept
Belatacept may be used for immuno- Weak
suppressive therapy in immunologically
low risk patients, who have a positive
Epstein-Barr virus serology.
Immunological complications
Immunological rejection is a common cause of early and late
transplant dysfunction. There is great variation in the timing
and severity of rejection episodes and how they respond to
treatment. Two main types of immunological reactions are
distinguished: T-cell mediated rejections (TCMR) and
antibody-mediated rejections (ABMR). Antibody-mediated
rejection and TCMR may be diagnosed together, called mixed
acute rejection. Antibody-mediated rejection may occur as
hyperacute rejection, acute rejection or chronic rejection.
Chronic ABMR is considered as one of the leading causes of
late graft loss.

Monitor transplant recipients for signs of Strong
acute rejection, particularly during the first
six months post-transplant.
Take regular blood samples in addition to Strong
regular monitoring of urine output and
ultrasound examinations in order to detect
graft dysfunction during hospitalisation.
Immediately rule out other potential causes Strong
of graft dysfunction in cases of suspected
acute rejection. An ultrasound of the
kidney transplant should be performed.
Perform a renal biopsy, graded according to Strong
the most recent Banff criteria, in patients
with suspected acute rejection episodes.

Only if contraindications to renal biopsy are Strong
present, can ‘blind’ steroid bolus therapy
be given.
Test patients who suffer acute rejection as Strong
soon as possible for anti-HLA antibodies
against the graft.
Re-assess the immunosuppressive therapy Strong
of all patients with rejection, including
patient adherence to the medication,
which is of particular importance in late
rejections.
Hyper-acute rejection
Hyper-acute rejection is the most dramatic and destructive
immunological attack on the graft. It results from circulating,
complement-fixing IgG antibodies, specifically reactive against
incompatible donor antigen, which engages with and destroys
the vascular endothelium within minutes or hours after
vascularisation.

Prevent hyper-acute rejection by adequate Strong
ABO blood group and HLA matching of
donor and recipients.
Treatment of T-cell mediated acute rejection

Use steroid bolus therapy as first-line Strong
treatment for T-cell mediated rejection in
addition to ensuring adequate baseline
immunosuppression.

In severe or steroid-resistant rejection, use Strong
intensified immunosuppression, high-dose
steroid treatment, and eventually T-cell
depleting agents.
Treatment of antibody mediated rejection

Treatment of antibody mediated rejection Strong
should include antibody elimination.
Follow-up after transplantation

Long-term graft function is of critical importance for the
success of a transplant. Therefore, regular long-term follow-up
by experienced transplant physicians is essential in order to
detect complications or graft dysfunction early and reassure
adherence to the immunosuppressive regimen.

Provide lifelong regular post-transplant Strong
follow-up by an experienced and trained
transplant specialist at least every six to
twelve months.
Advise patients on appropriate lifestyle Strong
changes, potential complications, and
the importance of adherence to their
immunosuppressive regimen.

Regularly monitor (approximately every four Strong
to eight weeks) serum creatinine, estimated
glomerular filtration rate, blood pressure,
urinary protein excretion, immunosuppres-
sion and complications after renal trans-
plantation. Changes in these parameters
over time should trigger further diagnostic
work-up including renal biopsy, a search for
infectious causes and anti-HLA antibodies.
Perform an ultrasound of the graft, in case Strong
of graft dysfunction, to rule out obstruction
and renal artery stenosis.
In patients with interstitial fibrosis and Strong
tubular atrophy undergoing calcineurin
inhibitor therapy and/or with histological
signs suggestive for calcineurin inhibitor
toxicity (e.g. arteriolar hyalinosis, striped
fibrosis) consider calcineurin inhibitor
reduction or withdrawal.
Initiate appropriate medical treatment, e.g. Strong
tight control of hypertension, diabetes,
proteinuria, cardiac risk factors, infections,
and other complications according to
current guidelines.

EAU Guidelines (ISBN 978-94-92671-01-1) available to all members of

EAU GUIDELINES ON
THROMBOPROPHYLAXIS IN
UROLOGICAL SURGERY
K.A.O. Tikkinen (Chair), R. Cartwright, M.K. Gould, R. Naspro, G.

Novara, P.M. Sandset, P.D. Violette, G.H. Guyatt
Introduction
Utilising recent studies and newly summarised evidence,
the EAU Guidelines on Thromboprophylaxis provide
practical evidence-based guidance regarding post-surgery
thromboprophylaxis and peri-operative management of
antithrombotic agents in urology.
The Thromboprophylaxis Panel used the Grading of

Recommendations Assessment, Development and Evaluation
(GRADE) approach for assessment of quality of evidence
and grading of recommendations. GRADE offers four levels
of e vidence quality, reflecting the degree of certainty or
confidence in the evidence: high, moderate, low, and very
low. The strength of a recommendation reflects the extent
to which we can be confident that desirable effects of an
intervention outweigh undesirable effects. GRADE classifies
recommendations as strong or weak.
Thromboprophylaxis post-surgery
This guideline provides procedure and patient risk-specific
guidance weighing the benefit of reduced venous
thromboembolism (VTE) against the harm of increased
bleeding. The Panel provides recommendations for numerous
urologic procedures, with variation across patient risk
strata (Table 1). When creating recommendations, the Panel
398 Thromboprophylaxis in Urological Surgery

first calculated the net benefit (absolute reduction in VTE
risk – absolute increase in bleeding risk) and then considered
quality of evidence for both pharmacological and mechanical
prophylaxis (Figure 1).
Table 1: Venous thromboembolism (VTE) according to patient

risk factors
Risk factors
Low risk No risk factors
Medium risk Any one of the following:
age 75 years or more;
body mass index 35 or more;
VTE in 1st degree relative (parent, full sibling,
or child).
High risk Prior VTE
Patients with any combination of two or
more risk factors
Thromboprophylaxis in Urological Surgery 399

Figure 1: Proportion of cumulative risk (%) of venous
thromboembolism (VTE) and major bleeding by week
since surgery during the first four post-operative
weeks
100
Proportion (%) of cumulative risk
Bleeding
80
VTE
60
40
20
0
0 7 14 21 28
Post-operative days
Proportion of 28-day
cumulative bleeding risk
Operation day 47.4%
Post-operative day 1 63.3%
The bleeding pattern depicted applies to most bleeds for

most surgeries. However, some urological surgeries, such
as transurethral resection of the the prostate (TURP), are
associated with later bleeding. This is typically minor and
occurs around ten days post-surgery.

General statements for all procedure-specific
recommendations
The following apply to all recommendations for
pharmacological prophylaxis:
• All recommendations are based on a starting time of the

morning after surgery.
• The optimal duration of pharmacological prophylaxis for
all recommendations is approximately four weeks post-
surgery.
• There are number of acceptable alternatives for
pharmacologic prophylaxis (Table 2).
• All recommendations for mechanical prophylaxis are until
ambulation.

Table 2: Alternative regimens for pharmacological
prophylaxis
Pharmacological agent Dosage*

Low molecular weight
heparins:
Dalteparin 5,000 IU injection once a day
Enoxaparin 40 mg injection once a day
Tinzaparin 3,500/4,500 IU injection once a day
Unfractionated heparin 5,000 IU injection two or three
times a day
Fondaparinux† 2.5 mg injection once a day
Direct acting oral
anticoagulants†:
Dabigatran 220 mg tablet once a day
Apixaban 2.5 mg tablet once a day
Edoxaban 30 mg tablet once a day
Rivaroxaban 10 mg tablet once a day
* Dosages may not apply in renal impairment.
† Fondaparinux and direct acting oral anticoagulants have not
been sufficiently studied in urology to warrant on-label use

for post-surgery thromboprophylaxis.

Recommendations for prophylaxis in specific
procedures according to patient risk
Ambulatory day surgery

R1. In all patients undergoing minor ambulatory day surgery
(for example, circumcision, hydrocelectomy and vasectomy),
the Panel recommends against use of pharmacological
prophylaxis (strong, moderate-quality evidence), and against
use of mechanical prophylaxis (strong, moderate-quality
evidence).
Open radical cystectomy

R2. In all patients undergoing open radical cystectomy, the
Panel recommends use of pharmacological prophylaxis
(strong, moderate or high-quality evidence depending
on risk stratum), and suggests use of mechanical
prophylaxis (weak, low-quality evidence).
Robotic radical cystectomy

R3. In all patients undergoing robotic radical cystectomy, the
Panel suggests use of pharmacological prophylaxis (weak,
low-quality evidence), and suggests use of mechanical
Laparoscopic radical prostatectomy

R4. For patients undergoing laparoscopic radical
prostatectomy without pelvic lymph node dissection (PLND),
for those at low risk of VTE, the Panel recommends against
use of pharmacological prophylaxis (strong, moderate-quality
evidence) and suggests against use of mechanical prophylaxis
(weak, low-quality evidence); for those at moderate and
high risk, the Panel suggests against use of pharmacological
prophylaxis (weak, moderate- or high-quality evidence) and
suggests use of mechanical prophylaxis (weak, low-quality
evidence).

prostatectomy with standard PLND, for those at low risk of
VTE, the Panel recommends against use of pharmacological
prophylaxis (strong, moderate-quality evidence); for
those at medium risk, the Panel suggests against use of
pharmacological prophylaxis (weak, moderate-quality
evidence); for those at high risk, the Panel recommends use of
pharmacological prophylaxis (strong, high-quality evidence);
and for all patients, the Panel suggests use of mechanical

prostatectomy with extended PLND, for those at low risk
of VTE, the Panel suggests against use of pharmacological
prophylaxis (weak, moderate-quality evidence); for those
at medium risk, the Panel suggests use of pharmacological
prophylaxis (weak, high-quality evidence); for those at
high risk, the Panel recommends use of pharmacological
prophylaxis (strong, high-quality evidence); and for all
patients, the Panel suggests use of mechanical prophylaxis
(weak, low-quality evidence).
Open radical prostatectomy

R7. For patients undergoing open radical prostatectomy
without PLND or with standard PLND, for those at low risk
of VTE, the use of pharmacological prophylaxis is suggested
(weak, moderate-quality evidence); for those at medium and
high risk, use of pharmacological prophylaxis is recommended
(strong, moderate- or high-quality evidence); and for all

R8. For all patients undergoing open radical prostatectomy
with extended PLND, the Panel recommends use of
pharmacological prophylaxis (strong, moderate or
high-quality evidence), and suggests use of mechanical
Robotic radical prostatectomy

R9. For patients undergoing robotic radical prostatectomy
without PLND, for those at low risk of VTE, the Panel
recommends against use of pharmacological prophylaxis
(strong, moderate-quality evidence) and suggests against
use of mechanical prophylaxis (weak, low-quality evidence);
for those at medium and high risk, the Panel suggests against
use of pharmacological prophylaxis (weak, moderate-quality
evidence) and suggests use of mechanical prophylaxis (weak,
low-quality evidence).

with standard PLND, for those at low risk of VTE, the Panel
recommends against use of pharmacologic prophylaxis
(strong, moderate-quality evidence); for those at medium
risk, the Panel suggests against use of pharmacologic
prophylaxis (weak, moderate-quality evidence); for those
at high risk, the Panel suggests use of pharmacologic
prophylaxis (weak, moderate-quality evidence); and for all

with extended PLND, for those at low risk of VTE, the Panel
suggests against use of pharmacologic prophylaxis (weak,
moderate-quality evidence); for those at medium risk, the
Panel suggests use of pharmacologic prophylaxis (weak,
moderate-quality evidence); for those at high risk, the Panel
recommends use of pharmacologic prophylaxis (strong,
moderate-quality evidence); and for all patients, the Panel
evidence).
Nephrectomy
R12. For patients undergoing laparoscopic partial
nephrectomy, for those at low and medium risk of VTE, the
Panel suggests against use of pharmacologic prophylaxis
(weak, low-quality evidence); for those at high risk, the Panel
recommends use of pharmacologic prophylaxis (strong,
moderate-quality evidence); and for all patients, the Panel
evidence).
R13. For all patients undergoing open partial nephrectomy,

the Panel suggests use of pharmacologic prophylaxis (weak,
very low quality evidence), and suggests use of mechanical
prophylaxis (weak, very low quality evidence).
R14. For patients undergoing robotic partial nephrectomy,

for those at low risk of VTE, the Panel suggests against use
of pharmacologic prophylaxis (weak, moderate-quality
evidence); for those at medium risk, the Panel suggests use
of pharmacologic prophylaxis (weak, moderate-quality
evidence); for those at high risk, the Panel recommends use
of pharmacologic prophylaxis (strong, high-quality evidence);
and for all patients, the Panel suggests use of mechanical

nephrectomy, for those at low or medium risk of VTE, the
(weak, very low quality evidence); for those at high risk, the
Panel suggests use of pharmacologic prophylaxis (weak, very
low quality evidence); and for all patients, the Panel suggests
use of mechanical prophylaxis (weak, very low quality
evidence).
R16. For patients undergoing open radical nephrectomy, the

Panel suggests use of pharmacologic prophylaxis (weak,
R17. For all patients undergoing radical nephrectomy with

thrombectomy, the Panel suggests use of pharmacologic
prophylaxis (weak, very low quality evidence), and suggests
use of mechanical prophylaxis (weak, very low quality
evidence).
R18. For all patients undergoing open nephroureterectomy,

the Panel suggests use of pharmacologic prophylaxis (weak,
prophylaxis (weak, very low quality evidence).
R19. For all patients undergoing primary nerve sparing

retroperitoneal lymph node dissection, the Panel suggests
use of pharmacologic prophylaxis (weak, very low quality
evidence), and suggests use of mechanical prophylaxis
(weak, very low quality evidence).

Non-cancer urological procedures
R20. For all patients undergoing transurethral resection of the
prostate (TURP) or equivalent procedures, the Panel suggests
against use of pharmacologic prophylaxis (weak, very low
quality evidence); for those at low or medium risk of VTE, the
Panel suggests against use of mechanical prophylaxis (weak,
low-quality evidence); and for those at high risk, the Panel
evidence).
R21. For patients undergoing laparoscopic donor nephrectomy

or open donor nephrectomy, for those at low risk of VTE, the
(weak, very low or low -quality evidence), and suggests
against use of mechanical prophylaxis (weak, very low or
low -quality evidence); for medium-risk patients, the Panel
suggests against use of pharmacologic prophylaxis (weak,
very low or low -quality evidence), and suggests use of
mechanical prophylaxis (weak, very low or low -quality
evidence); and for high-risk patients, the Panel suggests use
of pharmacologic prophylaxis (weak, very low or low -quality
evidence), and suggests use of mechanical prophylaxis
(weak, very low or low -quality evidence).
R22. For all patients undergoing open prolapse surgery or

reconstructive pelvic surgery, the Panel suggests against the
use of pharmacologic prophylaxis (weak, very low quality
evidence); for those at low or medium risk of VTE, the Panel
suggests against use of mechanical prophylaxis (weak, very
low or low -quality evidence); while for those at high risk, the
Panel suggests use of mechanical prophylaxis (weak, very low
or low -quality evidence).

R23. For all patients undergoing percutaneous
nephrolithotomy, the Panel suggests against use of
pharmacologic prophylaxis (weak, very low quality evidence);
for those at low or medium risk of VTE, the Panel suggests
against use of mechanical prophylaxis (weak, very low quality
evidence); while for those at high risk, the Panel suggests use
of mechanical prophylaxis (weak, very low quality evidence).
Peri-operative management of antithrombotic agents in

urology
In principle, there are four options to manage use of
antithrombotic agents (Figure 2) during the peri-operative
period:
1) t o defer surgery until antithrombotic agents are not
needed;
2) s top antithrombotic agents prior to surgery and restart
sometime after surgery;
3) continue through the surgical procedure;
4) a dminister alternative antithrombotic agents that may
still reduce the risk of thrombosis but with less risk
of bleeding than agents patients are currently using
(“bridging”).
Recent evidence has demonstrated that bridging increases

bleeding without preventing thrombosis. The Panel therefore
makes one of two recommendations for patients receiving
antithrombotic agents regularly and contemplating surgery:
1) discontinue antithrombotic therapy for the period
around surgery;
2) in those with a temporary very high risk of thrombosis,
delay surgery until that risk decreases. If it is not
possible to delay, continuing antithrombotic therapy or
bridging through surgery may be advisable.

Figure 2: The most widely used antithrombotic agents in
patients undergoing urologic surgery
Required period of stopping drug before surgery
(if desired) provided in parentheses.
Direct thrombin inhibitors Dabigatran (1–3 days)

UFH (12 hours)
Indirect thrombin inhibitors LMWH (12–24 hours)
Anticoagulant agents Fondaparinux (24 hours)
Atrial fibrillation and venous

Vitamin K antagonists Warfarin (3–5 days)
thrombosis, seldom arterial Apixaban (1–3 days)
thrombosis
Direct Xa inhibitors Edoxaban (1–3 days)
Rivaroxaban (1–3 days)
COX inhibitors Aspirin (3–7 days)

Abciximab (5 days)
Antiplatelet agents Glycoprotein IIb/IIIa inhibitors Eptifibatide (5 days)
Tirofiban (5 days)
Arterial disease, seldom venous
thrombosis Clopidogrel (5 days)
ADP inhibitors Prasugrel (5(–7) days)
Ticagrelor (5 days)
Recommendations for peri-operative management

Five days is an appropriate time to stop antiplatelet agents
before surgery, while the optimal time to stop varies across
anticoagulants (for details, see Figure 2).
R24. In all patients receiving antiplatelet agents (aspirin,

clopidogrel, prasugrel, ticagrelor), except those with very
high risk of thrombosis (see recommendations 26 and 27),
the Panel recommends stopping antiplatelet agents before
surgery and not initiating any alternative antithrombotic
therapy (strong, high-quality evidence).
R25. In patients in whom antiplatelet agents have been

stopped before surgery, the Panel recommends
restarting when bleeding is no longer a serious risk - typically
four days post-surgery - rather than withholding for longer
periods (strong, moderate-quality evidence).

R26. In patients with very high risk of thrombosis receiving
antiplatelet agents (those with drug-eluting stent placement
within six months, those with bare metal stent placement
within six weeks, those with transient ischemic attack (TIA)
or stroke within 30 days) in whom surgery can be delayed, the
Panel recommends delaying surgery (strong, high-quality
evidence).
R27. In patients with very high risk of thrombosis receiving

antiplatelet agents (those with drug-eluting stent placement
within six months, those with bare metal stent placement
within six weeks, those with TIA or stroke within 30 days)
in whom surgery cannot be delayed, the Panel suggests
continuing the drugs through surgery (weak, low-quality
evidence).
R28. In all patients receiving anticoagulant agents

(unfractionated heparin, low molecular weight heparin
[LMWH], warfarin, fondaparinux, dabigatran, apixaban,
rivaroxaban, edoxaban), except those with very high risk of
thrombosis (see recommendation 26), the Panel recommends
stopping drugs before surgery (see Figure 2) and not initiating
any alternative antithrombotic therapy (strong, high-quality
evidence).
Note: Patients with creatinine clearance <30 ml/min should
not receive dabigatran, apixaban, rivaroxaban or edoxaban.
R29. In patients in whom anticoagulants have been stopped

before surgery, the Panel recommends restarting
when bleeding is no longer a serious risk - typically four days
post-surgery - rather than withholding for longer periods
(strong, moderate-quality evidence).

R30. In patients with a new VTE, it is recommended that
surgery is delayed for at least one month, and if possible
three months, to permit discontinuation of anticoagulation
pre-operatively, rather than operating within one month of
thrombosis (strong, high-quality evidence).
R31. In patients receiving any anticoagulant with a severe

thrombophilia, such as antithrombin deficiency and
antiphospholipid antibody syndrome, the Panel suggests
anticoagulation with either heparin or LMWH through surgery,
rather than stopping anticoagulation before and after surgery
R32. In patients with high-risk mechanical prosthetic heart

valves, such as cage-ball valves, receiving warfarin, the Panel
recommends bridging with LMWH prior and subsequent
to surgery, rather than discontinuing anticoagulation
peri-operatively (strong, high-quality evidence).
Anticoagulation in these patients involves stopping the
warfarin five days prior, commencing LMWH four days
prior, omitting LMWH on the day of surgery, and
recommencing LMWH and warfarin after surgery.

EAU Guidelines (ISBN: 978-94-92671-01-1), available to all
members of the European Association of Urology at their
website: http://www.uroweb.org/guidelines/.

Disclaimer
The European Association of Urology (EAU) Clinical

Guidelines© published by the EAU Guidelines Office are
systematically developed evidence statements incorporating
data from a comprehensive literature review of the most
recent studies available (up to their publication date).
The aim of clinical guidelines is to help clinicians to make

informed decisions about their patients. However, adherence
to a guideline does not guarantee a successful outcome.
Ultimately, healthcare professionals must make their own
treatment decisions about care on a case-by-case basis, after
consultation with their patients, using their clinical judgement,
knowledge and expertise. A guideline is not intended to take
the place of physician judgment in diagnosing and treatment
of particular patients.
Guidelines may not be complete or accurate. The EAU

and their Guidelines Office, and members of their boards,
officers and employees disclaim all liability for the accuracy
or completeness of a guideline, and disclaim all warranties,
express or implied to their incorrect use. Guidelines users
always are urged to seek out newer information that might
impact the diagnostic and treatment recommendations
contained within a guideline.
Due to their unique nature – as international guidelines,

the EAU Guidelines are not embedded within one distinct
healthcare setting - variations in clinical settings, resources, or
common patient characteristics, are not accounted for.

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European

Clinical guidelines are a highly influential tool for improving

Going forward, a key aim of the EAU Guidelines office is to

The annual publication of the EAU Guidelines would not

We hope you find the 2018 update of the EAU Guidelines a

Prof. James N’Dow

Level of evidence and grading systems

1. t he overall quality of the evidence which exists for the

Table 1: Level of evidence*

Page 27 Urothelial Carcinoma of the Upper Urinary Tract

Page 37 Muscle-invasive and Metastatic Bladder Cancer

Page 53 Prostate Cancer

Page 79 Renal Cell Carcinoma

Page 101 Testicular Cancer

Page 120 Penile Cancer

Page 155 Urinary Incontinence

Page 179 Neuro-Urology

Page 208 Priapism

Page 217 Penile Curvature

Page 225 Male Infertility

Page 242 Male Hypogonadism

Page 253 Urological Infections

Page 273 Urolithiasis

Page 306 Paediatric Urology

Page 338 Urological Trauma

Page 355 Chronic Pelvic Pain

Page 378 Renal Transplantation

Page 398 Thromboprophylaxis in Urological Surgery

M. Babjuk (Chair), M. Burger (Vice-chair), E. Compérat,

Staging and classification systems

Non-muscle-invasive (TaT1, CIS) Bladder Cancer 9

10 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

The prognostic value of both WHO 1973 and 2004 grading

Table 2: WHO grading in 1973 and in 2004

1973 WHO grading

2004 WHO grading system (Papillary lesions)

Non-muscle-invasive (TaT1, CIS) Bladder Cancer 11

Recommendations for the primary Strength rating

12 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

Papillary (TaT1) tumours

Non-muscle-invasive (TaT1, CIS) Bladder Cancer 13

Recommendations for transurethral Strength rating

14 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

Non-muscle-invasive (TaT1, CIS) Bladder Cancer 15

16 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

Predicting disease recurrence and progression

Non-muscle-invasive (TaT1, CIS) Bladder Cancer 17

Risk category Definition Treatment

18 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

Subgroup of highest-risk tumours

*Low grade is a mixture of G1 and G2.

Non-muscle-invasive (TaT1, CIS) Bladder Cancer 19

20 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

General recommendations for adjuvant Strength rating

Non-muscle-invasive (TaT1, CIS) Bladder Cancer 21

22 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

Non-muscle-invasive (TaT1, CIS) Bladder Cancer 23

When planning the follow-up schedule and methods, the

24 Non-muscle-invasive (TaT1, CIS) Bladder Cancer

1. t he overall quality of the evidence which exists for the

Systemac screening during medical interview

Germ-line DNA sequencing: mutaon?

- Clinical evaluaon for other HNPCC-related cancer:

Single post-operave dose of intravesical

*In patients with a solitary kidney, consider a more

Diagnosis 1 – Males: biopsy apical prostac urethra

pT2N0M0 selected paents