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Community-Acquired Pneumonia Treatment 2017: Jordi Carratalà

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0% found this document useful (0 votes)
81 views28 pages

Community-Acquired Pneumonia Treatment 2017: Jordi Carratalà

Trr

Uploaded by

Dede Marizal
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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r y

a
Community-Acquired Pneumonia
r
i
Treatment 2017
L b
e ho r
I D ut
Jordi Carratalà

C M a
Department of Infectious Diseases
y
E S b
Hospital Universitari de Bellvitge

©
r y
r a
L ib
e ho r
I D ut
C M y a
E S b
©
Key points in the treatment of CAP
r y
r a

L ib
• e ho r
Time to initiation of antibiotic therapy

D t
Initial antibiotic treatment
I u

M a
Antibiotic de-escalation

C y

S b
Switching from IV to oral antibiotic therapy
E• ©
Duration of antibiotic treatment
Key points in the treatment of CAP
r y
r a

L ib
• e ho r
Time to initiation of antibiotic therapy

D t
Initial antibiotic treatment
I u

M a
Antibiotic de-escalation

C y

S b
Switching from IV to oral antibiotic therapy
E• ©
Duration of antibiotic treatment
r y
Studies assessing initiation of antibiotic therapy within various thresholds

a
and short-term mortality for hospitalized patients with CAP

r
L ib
e ho r
I D ut
C M y a
E S b
©
Lee JS. JAMA 2016
Key points in the treatment of CAP
r y
r a

L ib
• e ho r
Time to initiation of antibiotic therapy

D t
Initial antibiotic treatment
I u

M a
Antibiotic de-escalation

C y

S b
Switching from IV to oral antibiotic therapy
E• ©
Duration of antibiotic treatment
Recommended empirical antibiotic therapy for CAP
r y
r a
L ib
e ho r
I D ut
C M y a
E S b
©
IDSA/ATS Guidelines on the Management of CAP. CID 2007
Improving outcomes in elderly patients with CAP
r y
a
by adhering to national guidelines
r
ib
Aim: to define whether elderly patients hospitalized with CAP had better

L
e ho r
outcomes if they were were treated with empirical antimicrobial therapy
adherent the 2007 IDSA/AST guidelines
Design: secondary analysis of the CAPO database. 43 centers in 12
countries

I D ut
Patients: 1649 (975 regimen adherent, 465 undertreated, 195 overtreated)

C M
Outcome

y a
Clinical stability by 7 days
Adherence

71 %
Nonadherence

57 %
P

<.01

E S b
Length of stay, days 8 10 <.01

©
Overall in-hospital mortality 8% 17 % <.01

Arnold FW. Arch Intern Med 2009


Macrolide-based regimens and mortality in hospitalized
r y
a
patients with CAP: a systematic review and meta-analysis

r
ib
- 23 studies and 137574 patients were included.

L
e ho r
- Overall, macrolide use was associated with a significant mortality reduction
compared with nonmacrolide use (3.7% vs 6.5%; RR .78, 95% CI .64-.95; P= .01)

I D ut
- There was no survival advantage when analysis were restricted to RCTs or to
patients treated with guideline-concordant antibiotics.

C M y a
E S b
© RCTs

Asadi L. Clin Infect Dis 2012


Macrolides and mortality in critically ill patients with CAP:
r y
a
a systematic review and meta-analysis

r
ib
- 28 observational studies (no RCTs) of almost 10,000 critically ill pts with CAP.

L r
- Overall, macrolide use was associated with lower mortality compared with

e ho
nonmacrolides (21% vs. 24%; RR .82, 95% CI .70-.97; P= .02)
- When broadly guideline-concordant regimens were compared, no significant

I D ut
difference in mortality was found (20% betalactam/macrolide vs. 23% betalactam/
fluoroquinolone; RR .83, 95% CI .67-1.03; P= .09)

C M y a
E S b
©
Sligl WI. Crit Care Med 2014
β-Lactam Monotherapy vs β-Lactam–Macrolide
r y
r a
Combination Treatment in Moderately Severe CAP
A Randomized Noninferiority Trial

L ib
e ho r
I D ut
C M y a
E S b
© Garin N. JAMA Intern Med 2014
r y
r a
L ib
e ho r
Outcome
I D ut β-lactam β-lactam-macrolide (n= Fluoroquinolone (n=

C M
90-day mortality

y a (n= 656)
9.0 %
739)
11.1 %
888)
8.8 %

S b
Time to starting 4 (3 – 5) 4 (3 – 5) 3 (0 – 4)
oral ATB therapy
LOS
E
Complications
©
6 (4 – 8)
16.2 %
6 (4 – 10)
17.3 %

Cluster-randomized, crossover trial with strategies rotated


6 ( 4 – 8)
17.4 %

in 4-month periods; 7 hospitals in the Netherlands Postma DF. New Engl J Med 2015
Levofloxacin vs. azithromycin for treating Legionella pneumonia
r y
r a
ib
Observational retrospective multicenter study of 446 consecutive patients
with Legionella pneumonia requiring hospitalization (2000 – 2014)

L
Variable
e ho r Levofloxacin Azithromycin P

I D ut
Time to defervescence
(n= 175)

2 (1 – 4)
(n= 177)

2 (1 – 3) 0.45

C M y a
Time to clinical stability 3 (2 – 5) 3 (2 – 5) 0.48

LOS
E S b
Length of IV therapy 3 (2 – 5)

7 (5 – 10)
4 (3 – 6)

6 (5 – 9)
0.58

0.88

©
30-day mortality 2.3 % 5.1 % 0.16

Garcia-Vidal C. Clin Microbiol Infect 2017


Key points in the treatment of CAP
r y
r a

L ib
• e ho r
Time to initiation of antibiotic therapy

D t
Initial antibiotic treatment
I u

M a
Antibiotic de-escalation

C y

S b
Switching from IV to oral antibiotic therapy
E• ©
Duration of antibiotic treatment
Key points in the treatment of CAP
r y
r a

L ib
• e ho r
Time to initiation of antibiotic therapy

D t
Initial antibiotic treatment
I u

M a
Antibiotic de-escalation

C y

S b
Switching from IV to oral antibiotic therapy
E• ©
Duration of antibiotic treatment
Studies evaluating antibiotic de-escalation in CAP
r y
r a
Study

L ib Population De-escalation Results

Khasawneh
e ho r
60 pts with bacteremic CAP
n (%)
33 (55.5) No differences in
mortality and LOS

I D ut
Inf Drug Res 2014
261 pts with bacteremic CAP 165 (63.2) Higher mortality

M a
Carugati
in the non-DE

C
group

y
CMI 2015

S b
Yamana 11159 pts with CAP 1258 (11.3) No differences in
5-day and in-

E
J Infect 2016

Viasus

JAC 2016
© 1410 pts with CAPP 166 (11.7)
hospital mortality
No differences in
30-day mortality
Shorter LOS in DE
Key points in the treatment of CAP
r y
r a

L ib
• e ho r
Time to initiation of antibiotic therapy

D t
Initial antibiotic treatment
I u

M a
Antibiotic de-escalation

C y

S b
Switching from IV to oral antibiotic therapy
E• ©
Duration of antibiotic treatment
Effectiveness of early switch from intravenous to oral
r y
a
antibiotics in severe CAP: a multicentre randomised trial
r
ib
Setting: 7 teaching hospitals in the Netherlands.

L
e ho r
Participants: 265 pts in non-intensive care wards with severe CAP.
Intervention: 3 days of iv antibiotics followed, when clinically stable,

I D ut
by oral antibiotics or 7 days of iv antibiotics.

Outcome

C M y a Intervention
(n= 132)
Control
(n= 133)
Mean difference
(95% CI)

E S
Clinical cure
b 110 (83) 113 (85) 2% (-7% to 10%)

©
Mean (SD) LOS, days 9.6 (5.0) 11.5 (4.9) 1.9 (0.6 to 3.2)

Oosterheert JJ. BMJ 2006


Effect of a 3-step critical pathway to reduce duration of
r y
a
intravenous antibiotic therapy and length of stay in CAP

r
ib
Objective: to determine whether the use of a 3-step critical pathway

L
e ho r
is safe and effective in reducing duration of iv antibiotic therapy and
LOS in hospitalized adults with CAP

I D ut
Design: randomized controlled trial (ISRCTN 17875607)

C M y a
Setting: 2 tertiary hospitals in Barcelona
Intervention: 3-step critical pathway or usual care

S b
Primary end point: LOS

E ©
Secondary end points: duration of iv antibiotic therapy, adverse drug
reactions, need for readmission, and overall case-fatality rate
Carratalà J. Arch Intern Med 2012
3-Step Critical Pathway in CAP
r y
r a
L ib
1 EARLY MOBILIZATION

r
Movement out of bed:

e ho
> 20´ during the first 24 hours of hospitalization
progressive movement each subsequent day

I D ut
2 SWITCH TO ORAL ANTIBIOTIC THERAPY

C M y a
Ability to maintain oral intake, stable vital signs (temperature 37.8ºC,
RR 24´, SBP ≥90 mmHg) and absence of exacerbated comorbidities

S b
3 HOSPITAL DISCHARGE

E ©
Meeting criteria for oral antibiotic therapy, baseline mental status,
and adequate oxygenation on room air (PaO2 ≥60 mmHg or pulse
oximetry ≥90%)
Carratalà J. Arch Intern Med 2012
Effect of a 3-step critical pathway to reduce duration of
r y
a
intravenous antibiotic therapy and length of stay in CAP

r
Outcomes

L ib 3-step pathway Usual care P

Primary end pointe ho r (n= 200) (n= 201)

I D ut
Length of stay, median, days 3.9 6.0 <.001

M y a
Secondary end points

C
Length of iv antibiotic therapy 2.0 4.0 <.001

E S b
Adverse drug reactions 5% 16 % <.001
Phlebitis
©
Subsequent admission
4%
9%
10 %
8%
.02
.59
Overall case-fatality rate 2% 1% .45
Key points in the treatment of CAP
r y
r a

L ib
• e ho r
Time to initiation of antibiotic therapy

D t
Initial antibiotic treatment
I u

M a
Antibiotic de-escalation

C y

S b
Switching from IV to oral antibiotic therapy
E• ©
Duration of antibiotic treatment
Efficacy of short-course antibiotic regimens for
r y
a
community-acquired pneumonia: a meta-analysis
r

L ib
15 randomized controlled trials (1980-2006); mild/moderate CAP.

• e ho r
Short-course (≤ 7 days) versus extended-course (>7 days).

D ut
Short-course: azithro (10), β-lactams (2), FQ (2), ketolides (1).

M
Outcome I Relative risk, 95% CI

C y a
Clinical failure 0.89, 0.78 – 1.02

S
Mortality

E b 0.81, 0.46 – 1.43

©
Bacteriologic eradication 1.11, 0.76 – 1.62

Li JZ. Am J Med 2007


Duration of antibiotic treatment in CAP
r y
a
A multicenter randomized clinical trial

r

• ib
Multicenter, noninferiority, RCT. Four spanish teaching hospitals (2012 - 2013)

L r
A total of 312 pts were randomized at day 5 to an intervention (ATBs for 5 days)

e ho
or control group (duration of ATBs determined by physicians).

D ut
Outcome Control Intervention P value

I
Intent-to-treat analysis
Clinical success, n (%)

M
n= 150 n= 162

At day 10

C
At day 30

y a 71 (49)
132 (89)
90 (56)
147 (92)
0.18
0.33

S b
CAP symptom questionnaire

E
score, mean (SD)
At day 5

©
At day 30
24.7 (11)
18.6 (9.0)
27.2 (12)
17.9 (8)
0.10
0.69

Uranga A. JAMA Intern Med 2016


The new antibiotic mantra “Shorter is Better”
r y
r a
b
Infections for which short-course therapy has been shown

L i
to be equivalent in efficacy to longer therapy

r
e ho
I D ut
C M y a
E S b
©
Spellberg B. JAMA Intern Med 2016
Summary r y
r a

L ib
e ho r
Antibiotic therapy based on current guideline
recommendations should be initiated within 4

I D ut
to 8 hours of hospital arrival for patients with

C M y a
confirmed CAP.

• S
E b
Antibiotic de-escalation is effective in reducing
©
LOS and does not negatively affect outcomes.
Summary r y
r a

L ib
Objective measures of clinical stability can

e ho r
promote rapid transition from IV to oral

I D ut
antibiotic therapy, without compromising

• C M y a
outcomes, while decreasing LOS.

E S b
Duration of therapy in most patients can be

©
safely shortened to 5 days without increased
risk of treatment failure or mortality.
r y
a
Thank you very much for your attention!

r
L [email protected]

e ho r
I D ut
C M y a
E S b
© Santa Caterina Market, Barcelona

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