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Chemotherapy
Extravasation
Dr Nwosu EvanTherese
UNTH, Enugu
Introduction/ Definition
• Inadvertent administration of chemotherapeutic
drugs into surrounding perivascular tissues or
subcutaneous space rather than the vein
• There is usually a resulting injury
• Degree can be from very mild to sever and depends
on drugs
• It is a surgical oncology emergency
• Sever injury may need a skin graft or flap cover
• Management is multidisciplinary
Epidemiology
• According to Emiko et al ... Among 43,557 that
received chemotherapy 35 ( 0.08%) had
extravasation and duration was >2hrs
• There was an incidence of 4.7% to 6.5% according
to study done leon Alexander et . Al
• Zayneb Alami et al, morocco ; total of 18 patients;
7 females, 11 males out of 2000 0.9% incidence
Classification of
Chemotherapeutic agent
according to reactions to
tissue
• Neutrals : Inert or neutral compounds that do not
cause inflammation or damage
• Inflammitants : mild to moderate inflammation and
flare in local tissues
• Irritants: materials that cause reversible
inflammation or irritation to a body surface
• Vesicants: They are fluid or medication that causes
the formation of blisters with subsequent sloughing
of tissues occuring from the tissue necrosis
• E.g DNA binding; doxorubicin,
non-DNA binding vincristine
Flare reaction
• Symptoms reside within 30 mins with or without
treatment, may last 24 or 48hrs
Symptoms
• Immediate red blotches or streaks along the vein
puncture
• Local wheals
• Irritants near the site of injection
• Localised warmth and tenderness
• Localised erythma and edema
• Blood returns will occur with flare reaction
Classification
Vesicants
• Doxorubicin
• Epirubicin
• Paclitaxel
• Vincristine
• Vincristine
Irritants
• Carboplastin
• Etoposide
• Teniposide
Classification ctd
Inflammitants
• Fluorouracil
• Methotrexate
Neutrals
• Bleomycin
• Cyclophosphomide
• Cetuximab
• Asparginase
• Gencitabin
• Ifosfamide
Mechanism of injury
• Vasoconstriction= ischemic necrosis
• Osmotic pressure in cell membrane
• Ph related
• Cellular toxicity
• Mechanical compression
Risk factors ( patients factor)
• Small fragile veins
• Multiple treatment
• Generalised vascular disease
• Age
• Restlessness or confusion
• Impaired lymph flow and venous circulation
• SVC syndrome
• Impaired sensory perception
• Limited available veins
• Impaired sensory perception
• Obesity
Organisational factors
• Poor staff training
• Organisational issues
• Interruption or distraction during drug
administration
Drug related factor
• Vesicant potential
• Multiple vesicant
• Concentration of drugs
• Volume of drugs administered
• Chemical properties
Device factor
• High flow pressure
• Long infusion period
• Repeated use of same vein
• Multiple attempts at cannulation
• Unfavourable canulation site
• Poor choice of equipment
• Deeply implanted port
• Displacement or migration
Clinical presentation
• Burning stinging, pain or any acute change at the
injection site
• Induration erythema, venous discoloration or
swelling observd at the site
• Alteration to the rate of flow or increased
resistance to the administration of the cytotoxic
drugs that can not be explained by change in
postion of the body
• No blood return obtained
• Leakage from around the injection site
• Bleb formation or blisters
Evaluation
• Drug extravasated, dose ,volume
• Position and size of injury
• Amount and type of exudate
• Presence of swelling
• Pain
Grading
• Grade 1 painless edema
• Grade 11 erythma with associated symptoms
• Grade 111 ulceration or necrosis
• Grade 1v life threatening concequences
• Grade v death
Treatment of extravasation
• Monitor closely
• Instruct patient on alarm symptoms
• Stop infusion
• Call for help
• Do not remove canular
• Disconnect infussion
• Attempt aspiration of residual drug
• Elevate limb and immobilise
• Apply ice for some drugs
• Consider antidote
• Remove cannular
• Assesss for site, erthyma, induration
• Administer pain control
• Refer to plastic surgery , or specilist on affected part
• Debridement very important and should be early
• Document incidence
• Follow up for 2 weeks
Content of extravasation kit
• Inj hyaluronidase 1 ampoul / 1500iu
• Hydrocortisone1% cream
• S/ W for injection
• DMSO98% Solution
• Hot pack
• Cold pack
For port or CVAD
• Imaging may be needed
• Portogram may be done to ensure no fracture
Hyaluronidase
• Hyaluronidase for nonvesicant 200units in 2mls
dilute to 3:1 to NS subcute, intradermal
• Acts by dispersion of the drugs
• For vinblastine, vincrstine, vinflunine
• May partially work for paclitaxel
• Topical visafilator and intradermal terbutaline
• Dry cold compress for 20 to 30 min, 4x a day for 24
to 48hrs
• Apply dry warm compress 20 to 30min
Dimethyl sulfoxide (DMSO) 99%
Solution
• Works for doxorubicin, epirubicin, mitomycin
• Apply as soon as possible withim 10- 20mins
• Do not use with lysosomal doxorubicin
• Do not apply to wet skin
• Side effect inlude itching, erythma, characteritics
garlic breath odor
Warm compress
• Topical application for use in vinca alkaloid
• May decrease local drug concentration
• Increase blood flow which reduces pain
• Synergestic with hyaluronidase
Cold compress
• Management of vesicants or irritants with
exception of vinca alkaloid
• Use in oxaliplatin will execerbate sensory
neuropathy
Dexrazoxane
• Apply within 6 hours
• Prevents athracycline wound formation
• May show myelosuppresion
Prevention
• Avoids sites near joints and bone
• Do not give versicant into cubital fossa via
peripheral vein
• Frequent re-access the patency of the canaular
• Do not infuse in areas of poor venous return or
lymphatic drainage
• If vein punture is unsuccesful make a second
attempt in the opposite arm. Chose a proximal site
if same arm must be used
• Administer vesicant first
• Line should be free flowing
• Do not use infusion pump
• Observe for signs of infiltration
• Do not pinch the tubbing
• Flush line after drug admintration 20mls before
decanulation
• Select a small gauge cannular
• Ensure it can be visualised
• Site and secure adequately
• Do not use butter fly needle with vesicant
• Begine a new infusion for drug adminitration
Conclusion
• Chemotherapy extravasation is one of the
commonest complications in oncology
• Seems subtle but may have very adverse effect
• Increases mobility and mortality of oncology
patients
• Early diagnosis, early intervention is needed to
preserve the affected limb
• Good patient education, adequate staff training in
oncology management will reduce if not eliminate
it occurance in oncology centers
Reference
• Indian J plast surg 2023 oct;56(5):439-442 pubmed
journal article 38026779
• Emiko Sakaida etal Jpn J clin Oncol.2014 feb
• Zayneb Alami et al pan African medical journal(
ISSN:19378688
• Yuuka Shibata et al extravasation of non cytotoxic
agents, skin injury and risk classification . Jounal
home 2023volume 46 issue 6
• Leon Alexander et. Al Extravasation injuries: A
trivial injury often overlooked with disatrous
consequnces . World jounal of plastic Surg 2020
sep;9(3):326-330

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Chemotherapy Extravasation in Oncology 1.pptx

  • 2. Introduction/ Definition • Inadvertent administration of chemotherapeutic drugs into surrounding perivascular tissues or subcutaneous space rather than the vein • There is usually a resulting injury • Degree can be from very mild to sever and depends on drugs • It is a surgical oncology emergency • Sever injury may need a skin graft or flap cover • Management is multidisciplinary
  • 3. Epidemiology • According to Emiko et al ... Among 43,557 that received chemotherapy 35 ( 0.08%) had extravasation and duration was >2hrs • There was an incidence of 4.7% to 6.5% according to study done leon Alexander et . Al • Zayneb Alami et al, morocco ; total of 18 patients; 7 females, 11 males out of 2000 0.9% incidence
  • 5. • Neutrals : Inert or neutral compounds that do not cause inflammation or damage • Inflammitants : mild to moderate inflammation and flare in local tissues • Irritants: materials that cause reversible inflammation or irritation to a body surface • Vesicants: They are fluid or medication that causes the formation of blisters with subsequent sloughing of tissues occuring from the tissue necrosis • E.g DNA binding; doxorubicin, non-DNA binding vincristine
  • 6. Flare reaction • Symptoms reside within 30 mins with or without treatment, may last 24 or 48hrs Symptoms • Immediate red blotches or streaks along the vein puncture • Local wheals • Irritants near the site of injection • Localised warmth and tenderness • Localised erythma and edema • Blood returns will occur with flare reaction
  • 7. Classification Vesicants • Doxorubicin • Epirubicin • Paclitaxel • Vincristine • Vincristine Irritants • Carboplastin • Etoposide • Teniposide
  • 8. Classification ctd Inflammitants • Fluorouracil • Methotrexate Neutrals • Bleomycin • Cyclophosphomide • Cetuximab • Asparginase • Gencitabin • Ifosfamide
  • 9.
  • 10. Mechanism of injury • Vasoconstriction= ischemic necrosis • Osmotic pressure in cell membrane • Ph related • Cellular toxicity • Mechanical compression
  • 11. Risk factors ( patients factor) • Small fragile veins • Multiple treatment • Generalised vascular disease • Age • Restlessness or confusion • Impaired lymph flow and venous circulation • SVC syndrome • Impaired sensory perception • Limited available veins
  • 12. • Impaired sensory perception • Obesity
  • 13. Organisational factors • Poor staff training • Organisational issues • Interruption or distraction during drug administration
  • 14. Drug related factor • Vesicant potential • Multiple vesicant • Concentration of drugs • Volume of drugs administered • Chemical properties
  • 15. Device factor • High flow pressure • Long infusion period • Repeated use of same vein • Multiple attempts at cannulation • Unfavourable canulation site • Poor choice of equipment • Deeply implanted port • Displacement or migration
  • 16. Clinical presentation • Burning stinging, pain or any acute change at the injection site • Induration erythema, venous discoloration or swelling observd at the site • Alteration to the rate of flow or increased resistance to the administration of the cytotoxic drugs that can not be explained by change in postion of the body • No blood return obtained • Leakage from around the injection site • Bleb formation or blisters
  • 17. Evaluation • Drug extravasated, dose ,volume • Position and size of injury • Amount and type of exudate • Presence of swelling • Pain
  • 18. Grading • Grade 1 painless edema • Grade 11 erythma with associated symptoms • Grade 111 ulceration or necrosis • Grade 1v life threatening concequences • Grade v death
  • 19. Treatment of extravasation • Monitor closely • Instruct patient on alarm symptoms • Stop infusion • Call for help • Do not remove canular • Disconnect infussion • Attempt aspiration of residual drug • Elevate limb and immobilise • Apply ice for some drugs
  • 20. • Consider antidote • Remove cannular • Assesss for site, erthyma, induration • Administer pain control • Refer to plastic surgery , or specilist on affected part • Debridement very important and should be early • Document incidence • Follow up for 2 weeks
  • 21. Content of extravasation kit • Inj hyaluronidase 1 ampoul / 1500iu • Hydrocortisone1% cream • S/ W for injection • DMSO98% Solution • Hot pack • Cold pack
  • 22. For port or CVAD • Imaging may be needed • Portogram may be done to ensure no fracture
  • 23.
  • 24. Hyaluronidase • Hyaluronidase for nonvesicant 200units in 2mls dilute to 3:1 to NS subcute, intradermal • Acts by dispersion of the drugs • For vinblastine, vincrstine, vinflunine • May partially work for paclitaxel • Topical visafilator and intradermal terbutaline • Dry cold compress for 20 to 30 min, 4x a day for 24 to 48hrs • Apply dry warm compress 20 to 30min
  • 25. Dimethyl sulfoxide (DMSO) 99% Solution • Works for doxorubicin, epirubicin, mitomycin • Apply as soon as possible withim 10- 20mins • Do not use with lysosomal doxorubicin • Do not apply to wet skin • Side effect inlude itching, erythma, characteritics garlic breath odor
  • 26. Warm compress • Topical application for use in vinca alkaloid • May decrease local drug concentration • Increase blood flow which reduces pain • Synergestic with hyaluronidase
  • 27. Cold compress • Management of vesicants or irritants with exception of vinca alkaloid • Use in oxaliplatin will execerbate sensory neuropathy
  • 28. Dexrazoxane • Apply within 6 hours • Prevents athracycline wound formation • May show myelosuppresion
  • 29.
  • 30. Prevention • Avoids sites near joints and bone • Do not give versicant into cubital fossa via peripheral vein • Frequent re-access the patency of the canaular • Do not infuse in areas of poor venous return or lymphatic drainage • If vein punture is unsuccesful make a second attempt in the opposite arm. Chose a proximal site if same arm must be used
  • 31. • Administer vesicant first • Line should be free flowing • Do not use infusion pump • Observe for signs of infiltration • Do not pinch the tubbing • Flush line after drug admintration 20mls before decanulation
  • 32. • Select a small gauge cannular • Ensure it can be visualised • Site and secure adequately • Do not use butter fly needle with vesicant • Begine a new infusion for drug adminitration
  • 33.
  • 34. Conclusion • Chemotherapy extravasation is one of the commonest complications in oncology • Seems subtle but may have very adverse effect • Increases mobility and mortality of oncology patients • Early diagnosis, early intervention is needed to preserve the affected limb • Good patient education, adequate staff training in oncology management will reduce if not eliminate it occurance in oncology centers
  • 35. Reference • Indian J plast surg 2023 oct;56(5):439-442 pubmed journal article 38026779 • Emiko Sakaida etal Jpn J clin Oncol.2014 feb • Zayneb Alami et al pan African medical journal( ISSN:19378688 • Yuuka Shibata et al extravasation of non cytotoxic agents, skin injury and risk classification . Jounal home 2023volume 46 issue 6
  • 36. • Leon Alexander et. Al Extravasation injuries: A trivial injury often overlooked with disatrous consequnces . World jounal of plastic Surg 2020 sep;9(3):326-330