Chemotherapy Extravasation Guidelines V8 6.14
Chemotherapy Extravasation Guidelines V8 6.14
Chemotherapy Extravasation Guidelines V8 6.14
Definitions
Extravasation is the inadvertent leakage of intravenous drugs out of the vein into surrounding tissues.
Extravasation injury refers to the damage caused by the leakage of solutions from the vein into the surrounding tissue
spaces. Depending on the substance that is extravasated into the tissue, the degree of injury can range from a very
mild skin reaction to severe necrosis.
The term Infiltration is sometimes used instead of extravasation to refer to the inadvertent administration of non-vesicant
solution/medication into surrounding tissues. Whilst the medication itself cannot damage the tissues, if the volume of fluid is
large, the swelling can result of compression of the nerve. Therefore the site must be observed and the degree of swelling
documented. The patient should be questioned regarding any numbness or loss of sensation in the affected limb and this
should be reported accordingly.
Flare is a localised inflammatory reaction characterised by a localised erythema, venous streaking and pruritus along the
injected vein. This is distinguishable from extravasation by the absence of pain and swelling and may include the presence
of a blood return.
Prevention of Extravasation
Forethought, planning and improved prevention measures can minimise the risk of extravasation.
i)
Careful assessment of the most appropriate cannulation site should be undertaken before insertion. Siting the
cannula over joints should be avoided, as tissue damage in these areas has serious consequences. If venous
access proves difficult, the opinion of an experienced practitioner should be sought as placement of a central
venous access device (CVAD) may be necessary.
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ii) Extravasation can occur in CVADs, often with delayed onset, and can be recognised by the patient complaining of
thrombocytopenic patients, diabetics with peripheral neuropathy and patients who have had previous
chemotherapy / radiotherapy. Non-English speaking patients and those with communication difficulties are also at
risk. Extra care should be taken with all these patient groups.
iv) Vesicant drugs in a chemotherapy regimen must be given before the other cytotoxic agents.
v) When given peripherally, bolus doses (in syringes) of vesicants must be given via a fast running infusion of a
compatible fluid. Continually assess the cannulation site throughout the administration for signs of swelling, pain or
inflammation, and monitor the fast running infusion for change in rate.
vi) Only the following vesicant cytotoxics may be given by peripheral infusion (in bags): paclitaxel, vinca alkaloids,
dacarbazine, streptozocin. However, the central venous route minimises the extravasation risk, and should be
considered on an individual patient basis. Any other cytotoxic vesicant infusions (in bags) should be administered
via a CVAD.
vii) Anthracycline administration must be carried out during normal working hours except in situations of life
threatening urgency, in which case direct Consultant authorisation is required and the reasons recorded in the
medical notes, as well as subsequent routine review of such episodes by the local chemotherapy group.
All out-patient and day case appointments for anthracycline administration should be scheduled for the
morning or early afternoon, so that all management options can be considered in the event of an anthracycline
extravasation.
All pre-planned out-of-hours anthracycline administration for AML should be delivered via a central venous
access device, again except for exceptional situations when direct Consultant authorisation is required and
reasons documented.
The patient complains of burning, stinging, or any discomfort / pain at the injection site. This should be
distinguished from a feeling of cold that may occur with some drugs.
Observation of swelling or induration at the device insertion site or along the tunnel/around port pocket or into
the shoulder and neck on the side of the port or catheter OR redness or blistering at the device insertion site.
This should be distinguished from the nettle rash effect seen with anthracyclines.
Withdraw as much of the drug as possible, via existing cannula or central venous access device (CVAD).
Mark area of skin with indelible pen. Take a photograph of the area as soon as possible. (Cameras are
often available from Accident & Emergency departments)
If appropriate, remove the peripheral cannula (do not remove the CVAD).
Refer to Appendix C to establish: whether a hot pack or cold pack should be used, or whether neither is
required; and what further treatment is recommended. Follow guidance in flow chart below accordingly.
Note that for Neutral drugs, neither a cold pack nor a hot pack is required. Aspirate as much fluid as
possible, and then remove the peripheral cannula. No further treatment should be required. Manage the
situation symptomatically. Document the incident in the patients notes.
OR
Document the incident by completing trust incident form and extravasation record form.
File copies in patients health record.
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Subsequent action
Patient follow up arrangements will be dependent upon the type of drug and volume that extravasated, and will
be decided by a practitioner who has experience of extravasation management.
Extravasation of vesicant and exfoliant drugs requires completion of the Follow up Flow Chart in Appendix D.
Notes:
* Use of 98% dimethyl sulfoxide (DMSO)
Draw around area of extravasation with indelible pen. Then, a thin layer of 98% DMSO solution should be
applied topically to the extravasated area using the applicator provided. Contact with good skin should be
minimised, as there are some reports associating DMSO with blistering of the skin. Once DMSO dries, apply
1% hydrocortisone cream and 30 minutes of cold compression. This process (DMSO, hydrocortisone cream,
cold compression) should be repeated as above every 2 hours for the first 24 hours.
After 24 hours of the above, for the next 7 days, 98% DMSO should be applied every 6 hours alternating with 6
hourly applications of 1% hydrocortisone cream, so that a preparation is being applied every 3 hours overall.
For patients receiving chemotherapy at RSCH, a Consultant plastic surgeon should be contactable via RSCH
switchboard. If unavailable via this route, contact the consultant plastic surgeon secretary at RSCH or St
Georges for further advice.
For patients receiving chemotherapy at SASH, contact the Plastics SpR on-call at Queen Victoria Hospital
(switchboard tel 01342 414000).
For FPH and ASPH patients, contact the Consultant plastic surgeon at Chelsea & Westminster hospital via the
C&W switchboard (tel 0208 7468000). At FPH, there is also a plastic surgeon secretary on site, who is
available in normal working hours on ext 4160.
For the saline flush-out, the patient will usually need to travel to the hospital where the plastic surgeons are
based. As the procedure is potentially limb-saving (mention this to the ambulance service), an
emergency ambulance should be requested for the transfer.
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*** Guidance for prescribing of dexrazoxane (Savene) - for use in Adults only
Dexrazoxane is a DNA topoisomerase II drug that protects against tissue damage with certain anthracyclines:
doxorubicin, epirubicin, daunorubicin and idarubicin.
Side effects include nausea (very common) and neutropenia/thrombocytopenia (common).
It MUST ONLY be prescribed in the following circumstances:
If there is a suspected peripheral extravasation of 5ml or more of doxorubicin, epirubicin, daunorubicin or
idarubicin.
OR
There is an extravasation of doxorubicin, epirubicin, daunorubicin or idarubicin via the central venous route.
The case must be discussed with the Trust Lead Chemotherapy Nurse, or the Senior Chemotherapy Sister, as
well as the patients Consultant, before Savene is prescribed.
See Appendix G for more details with regards to prescribing dexrazoxane.
Dexrazoxane (Savene) is a cytotoxic drug. It must therefore be reconstituted in a pharmacy aseptic unit.
The Savene pre-printed prescription, which is available in Appendix H, should be used for prescribing.
St Lukes Pharmacy to fax prescription to the Pharmacy Aseptic Unit for reconstitution
Prepared dose delivered to clinical area for administration
Pharmacy Department at relevant Trust to fax an order to RSCH Pharmacy Aseptic Unit for Savene
reconstitution. Receipt of this fax should be confirmed by telephone.
Transport should be organised by RSCH pharmacy staff, according to Appendix J. The urgent nature of
the delivery should be highlighted in order that the 6 hour window of efficacy is not breached, and a
transport collection time agreed.
The pre-prepared Savene dose is transported to a pre-specified location at ASPH, FPH or SASH.
RSCH will invoice the Trust for the Savene, via the usual mechanism for invoicing chemotherapy.
Savene cannot be considered as a treatment option. An urgent plastic surgeon referral for a saline flushout should be considered.
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References:
Allwood M, Stanley A, Wright P; Cytotoxics Handbook 4th Ed. Radcliffe Medical Press: Oxford 2002
European Oncology Nursing Society (EONS) Extravasation Guidelines 2007
Dougherty, L and Lister, S. RMH Manual of Clinical Nursing Procedures 8th Edition (2011)
1Gault, DT; Br J Plast Surg 1993; 46: 91 96
Mouridsen, H et al; Annals of Oncology 2007; 18: 546 550
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APPENDIX A:
Exfoliants*
Group 2
Cisplatin
Irritants
Group 3
Bendamustine
Inflammitants
Group 4
Fluorouracil
Neutrals
Group 5
Alemtuzumab
Cabazitaxel
Liposomal
Daunorubicin
Carboplatin
Methotrexate
Asparaginase
Carmustine
Docetaxel
Dexrazoxane
Raltitrexed
Bevacizumab
Dacarbazine
Liposomal
Doxorubicin
Etoposide
Bleomycin
Dactinomycin
Mitoxantrone
Irinotecan
Bortezomib
Daunorubicin
Oxaliplatin
Cetuximab
Doxorubicin
Topotecan
Cladribine
Epirubicin
Cyclophosphamide
Idarubicin
Cytarabine
Mitomycin
Eribulin
Paclitaxel
Fludarabine
Streptozocin
Gemcitabine
Treosulfan
Ifosfamide
Vinblastine
Ipilimumab
Vincristine
Melphalan
Vindesine
Pemetrexed
Vinflunine
Pentostatin
Vinorelbine
Rituximab
Trastuzumab
Definitions:
*Vesicants:
Drugs which are capable of causing pain, inflammation and blistering of the local skin,
underlying flesh and structures, leading to tissue death and necrosis
*Exfoliants:
Drugs which are capable of causing inflammation and shedding of the skin, but less likely to
cause tissue death
Irritants:
Drugs which are capable of causing inflammation, irritation or pain at site of extravasation, but
rarely cause tissue breakdown
Inflammitants:
Drugs which are capable of causing mild to moderate inflammation and flare in local tissues
Neutrals:
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Hot Pack
Cold Pack
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APPENDIX C: Chart of cytotoxic drugs according to immediate treatment in the event of extravasation:
Drug
Amsacrine
Bendamustine
Bleomycin
Bortezomib
Cabazitaxel
Carboplatin
Carmustine
Cisplatin
Cladribine
Cyclophosphamide
Cytarabine
Dacarbazine
Dactinomycin
Daunorubicin
Docetaxel
Doxorubicin
Epirubicin
Eribulin
Etoposide
Fludarabine
Fluorouracil
Gemcitabine
Idarubicin
Ifosfamide
Irinotecan
Liposomal, Daunorubicin
Liposomal, Doxorubicin
Melphalan
Methotrexate
Mitomycin
Mitoxantrone
Oxaliplatin
Paclitaxel
Pemetrexed
Pentostatin
Pixantrone
Raltitrexed
Streptozocin
Topotecan
Treosulfan
Vinblastine
Vincristine
Vindesine
Vinflunine
Vinorelbine
Cold/Warm pack
Cold
Cold
None
None
Warm
Cold
Cold
Cold
None
None
None
Cold
Cold
Cold
Warm
Cold
Cold
None
Cold
None
Cold
None
Cold
None
Cold
Cold
Cold
None
Cold
Cold
Cold
Warm
Warm
None
None
None
Cold
Cold
Cold
Cold
Warm
Warm
Warm
Warm
Warm
Treatment
Hydrocortisone cream
Hydrocortisone cream
No antidote
No antidote
Hyaluronidase
Hydrocortisone cream
Hydrocortisone cream
Hydrocortisone cream
No antidote
No antidote
No antidote
Hydrocortisone cream
DMSO
DMSO (*but see below)
Hyaluronidase
DMSO (*but see below)
DMSO (*but see below)
No antidote
Hydrocortisone cream
No antidote
Hydrocortisone cream
No antidote
DMSO (*but see below)
No antidote
Hydrocortisone cream
DMSO (for 10 14 days)
DMSO (for 10 14 days)
No antidote
Hydrocortisone cream
DMSO
DMSO
Hyaluronidase
Hyaluronidase
No antidote
No antidote
No antidote
Hydrocortisone cream
Hydrocortisone cream
Hydrocortisone cream
Hydrocortisone cream
Hyaluronidase
Hyaluronidase
Hyaluronidase
Hyaluronidase
Hyaluronidase
*For 5ml volume peripheral extravasation, or any central extravasation, of an anthracycline, Savene may be a more
appropriate alternative. Discuss with the Lead Chemotherapy Nurse or Day Centre Manager
If an extravasation occurs and the drug is not listed above, please contact pharmacy for classification and advice.
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Hospital number:
Burning
Stinging
Other acute changes
Yes / No
Yes / No
Yes / No - If answer is Yes, please specify:
Indurated
Swollen
Red
Blistered
Yes / No
Yes / No
Yes / No
Yes / No
c) Was there:
Blood return
Yes / No
Resistance on plunger of bolus syringe
Yes / No
Absence of free flow of infusion
Yes / No
Please now document the Emergency Nursing Management section before completing the rest of this form
4) Bolus or infusion? (Please circle one)
5) Type of device: Cannula / Other (Please specify, including gauge)
6) Was a pump being used?
Yes / No
Clinical Area:
Signature:
Date:
Please photocopy this form and send one copy with the Trust incident form and place one copy in the
patients notes
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Hospital number:
Name of Drug(s):
Nursing Management
Yes / No
Yes / No
Yes / No
Yes / No
Name of doctor
informed:
Yes / No
Yes / No
Date and
Time
Nurse
Signature
Yes / No
Yes / No
Yes / No
Yes / No
Yes / No
Yes / No
Yes / No
Yes / No
Yes / No
Yes / No
Please photocopy this form and send one copy with the Trust incident form and place one copy in the
patients notes
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Hospital Number:
Ward:
14
21*
28*
35*
42*
Date
Call / Visit
Skin Colour
Skin Temperature
Skin Integrity
Oedema
Mobility
Pain
Fever
Nurse Initials
* May be omitted if signs and symptoms of extravasation resolved
Grading Scale
Skin Colour
0
Normal
1
Pink
2
Red
3
Blanched
area
surrounded
by red
4
Blackened
Skin Integrity
Unbroken
Blistered
Superficial
skin loss
Skin Temp.
Normal
Warm
Hot
Oedema
Absent
Non-pitting
Pitting
Mobility
Full
Slightly
limited
Very Limited
Pain
Fever
Immobile
Elevated
Please photocopy and place one copy in patients notes and attach one copy to Trust Incident Form
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APPENDIX E:
What is extravasation?
Extravasation is the leakage (or accidental infiltration) of drugs outside of the vein and into the surrounding tissues.
This can lead to an immediate painful reaction, and may with some drugs result in local tissue damage. You may have
noticed pain, stinging, swelling or other changes to the skin at the site of drug administration, or the nurse may have
noticed that the drug was not flowing in easily.
Why did this happen?
Extravasation is a rare but known complication of intravenous chemotherapy. It is impossible to prevent this even
though we take all possible precautions. The important thing is that it has been detected and treated.
Why is extravasation a problem?
It can lead to pain, stiffness and tissue damage.
What treatment have I received to prevent tissue damage?
The nurse has given you the recommended treatment for the extravasation. Although this will help to minimise the
chance of developing further problems, you will need to keep checking the area every day.
Checking the area
Once a day, check the area for the following:
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PHARMACY DEPARTMENT
Patient Name:
Hospital Number:
Consultant:
Date:
DMSO must be prescribed on the drug chart.
Please give this sheet to your pharmacist for replacement supply. The product may only be replaced if the above
details have been completed.
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(max 2000mg)
(max 2000mg)
(max 1000mg)
Dexrazoxane is a cytotoxic drug and therefore may only be reconstituted in a pharmacy aseptic unit.
It has a short shelf life once reconstituted (4 hours at 2 8oC).
The patient must be consented for dexrazoxane, as it is a cytotoxic.
The prescription should be written using the template in Appendix H.
Dexrazoxane may only be administered by a trained chemotherapy nurse.
Each dose should be infused, in 500ml of buffered diluent provided with the Savene, over 1 2 hours.
Day 2 and Day 3 doses should be given at the same time of day (+/- 3 hours) as Day 1.
Special precautions for the administration of Dexrazoxane (Savene):
The first dose must be administered as soon as possible, and initiated within 6 hours of extravasation.
Cooling and DMSO should not be used in combination with treatment with dexrazoxane (local cooling should be
removed at least 15 minutes prior to administration) as they may interfere with efficacy of dexrazoxane. Hydrocortisone
cream should also not be used.
The patient should be cannulated in the opposite arm to the extravasation wherever possible or, if this is not possible,
higher than the site of extravasation.
This current cycle of chemotherapy must be discontinued and not restarted until at least 48 hours following day 3
infusion. The consultant must be informed as soon as possible as they will need to consider re- prescribing the cycle
of chemotherapy.
It is not recommended in children (age < 18 years) or in patients with hepatic or renal impairment (CrCl <
40ml/min).
It is generally not recommended in combination with live attenuated vaccines or with phenytoin.
Patients at risk of hyperkalaemia should be monitored for plasma potassium levels. It also contains sodium which may
be harmful to patients who have a raised sodium level.
Patients on anticoagulants should be monitored more frequently i.e. daily whilst patient receiving dexrazoxane.
Local examination (for phlebitis and local injection site pain) and haematological monitoring should be performed on a
regular basis (e.g. daily) after treatment until resolution.
Patient referral to a plastic surgeon for assessment of the extravasation injury within 7 days after the extravasation is
mandatory.
This is an expensive drug; therefore you should seek guidance for prescribing from your Lead Chemotherapy Nurse or Day
Centre Manager, and consult the dexrazoxane algorithm below.
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YES
NO
Is it an adult or child?
ADULT
CHILD (< 18
years)
YES
YES
NO
2.
2.
3.
3.
Post Administration
Page 16 of 18
CONSULTANT:
CHEMOTHERAPY REGIMEN:
ALLERGIES:
Ht:
Wt:
kg
BSA:
m2
Patient Name:
Address:
DOB:
Hospital Number:
LOCATION:
Dose
Route
Administration
details
*Ondansetron
8 mg
PO
*Dexamethasone
8 mg
PO
Drug
DAY
1
DAY
2
DAY
3
IV
Dexrazoxane
1000 mg/m2
(Max 2000 mg)
mg
Ondansetron
8 mg
PO
Dexamethasone
8 mg
PO
Dexrazoxane
1000 mg/m2
(Max 2000 mg)
mg
IV
Ondansetron
8 mg
PO
Dexamethasone
8 mg
PO
Dexrazoxane
500 mg/m2
(max 1000mg)
CONFIRMED BY:
mg
DATE:
IV
Prescriber
sig. & date
Date
given
Time
given
DATE:
FAXED:
Sig. of
nurse
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