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Guidelines of extravasation, infection &pain
management in Oncology
Dr. O.P. Singh M.D.FICRO.
Prof & H.O.D
(Radiotherapy)
Gandhi Medical College Bhopal
, India
Dr. Gopa Ghosh M.D,
Associate prof (Radiotherapy)S.S. Medical
College Rewa ,India
Extravasation can be defined as
leakage of drug in to subcutaneous
tissue which leads to either irritation
or vescication.
Classification of Cytotoxic drugs
according to local site reaction
1.Irritan
ts
Inflamm
ation,irr
itation,
Pain
2.Inflam
mitants
Inflamma
tion/flare
3.Exfolia
nts
Shedding
/Exfoliati
on of
skin ,no
necrosis
4.Vescica
nts
Tissue
Ulceratio
n&necros
is
5.Neutrals do not cause any damage
Extravasation of a vescicant is a
medical emergency hence calls
for early detection &prompt
action to prevent functional loss
of limb involved.
Common Exfoliants &
Vescicants
Exfoliants
Liposomal
Daunorubicin
Liposomal
doxorubicin
Cisplatin
Mitoxantrone
Oxalaplatin
Vescicants
Doxorubicin
Daunorubicin
Epirubicin
Dactinomycin
Mitomycin C
Vincristine
Vinblastine
Paclitaxol
Probable risk factors for
Peripheral
Extravasation:
Thin fragile veins
Site of cannulation
Peripheral neuropathy(Diabetes)
Excessive movements due to altered mental
status,vomitting,coughing
SVC Syndrome
Elderly/ Paediatric
Obese
Prior chemotherapy
Cause of Central venous catheter
leakage
Backflow secondary to thrombosis in the catheter.
Needle dislodgement from the port
Damage of the catheter
Thrombocytopenia
Prevention of extravasation
 Careful assesment of cannulation site
 Cannulation over joints to be avoided
 Patients at increased risk of extravasation should be
identified.
 Vescicant drugs to be given before other drugs
 Bolus doses are given via fast running infusion of
compatible fluid
Continuous observation of cannulation site for signs of
swelling ,pain inflammation, slowing of drip rate.
Opinion for placement of CVAD should be sought if
Peripheral access difficult.
Extravastion can also occur in central access often of
delayed onset .
Signs/Symptom's
Burning ,stinging ,pain at injection site
Swelling ,redness , blister.
Absence of free flow of infusion
Resistance on the plunger of the syringe in
case of bolus drug infusion
No blood return in the cannula.
Steps in management of
extravasation
Stop infusion ,disconnect tubing
Withdraw as much as drug possible via existing
cannula or CVAD
Mark skin area with indelible pen
Take photograph of the area
Open extravasation kit
Apply hot/cold pack as applicable for the concerned
drug.
 Elevate the limb
 Inform treating oncologist
 Urgent assesment by oncologist regarding referral to
plastic surgeon for saline flush out of extravasated
area.
 Follow up at regular intervals.
Contents of extravasation kit
 Inj Hyaluronidase (1ampoule/1500iu)
 Hydrocortisone 1%cream
 S/w for injection
 DMSO98%solution
 Hot pack
 Cold pack
Drugs vs. Warm/Cold pack
Vinca alkoids, Paclitax, Oxaloplatin
Hyaluronidase+ Warm pack
Anthracyclins,Mitoxantrone,Mitomycin,Dacti
nomycinColdpack+DMSO+1%hudrocortis
one
cream
Carboplat,Cisplat,Etoposide,5FU,Irrinotican,
Mtx- Coldpack & Hydrocortisone cream
Regime of Warm & Cold pack
Warm
1amp Hyaluronidase
s.c. inj

Warm pack to aid in
absorption

Leave warm pack in
situ for 2-4hrs
Cold
cold pack +
Hydrocortison ecream
3days

Hydrocortisone
1%cream tds
 OR
Cold pack +
hydrocortisone cream
+ DMSO
DMSO application regime
Thin layer 98% DMSO1%hydrocortisoneCold
compress
Rpt every2hr/24hrs

DMSO 6hrly7days

Alt toDMSO1% Hydrocortisone 6 hrly7days
Cancer pain a matter of
concern
 60-80% of terminal cancer patients have severe pain
 Moderate pain exists in earlier course of the disease
also.
 QOL of such patients are significantly impaired due to
pain.
 Chronic pain expressed in vague terms (stiffness
,anxiety ,insomnia), actual prevalance underestimated
 85% cases can be pain free with modern drugs &
techniques.
Etiology
1. Direct infiltration to mucosa, soft tissues ,nerve
&bone.
2.Treatment related (Sx/RT/CT) accounts for 20%
pain cases.
 Pain produced- stimulation of peripheral pain
receptors.(nociceptive)
Neurogenic/Neuropathic-( involvement of
afferent nerves or nerve pathways.)
Broad Principles of drug treatment
Simplest dosage and least invasive route to be used
first
Analgesics to be given preferably around the clock basis
than as need basis for more effective pain control.
Opioid dose  till ultimate pain relief or unacceptable
side effects.
NAIDS &adjuvant analgesics with ceiling effect, dose
till upper limit of recommended dose
Switching of analgesics when required
 Primary cause of pain i.e. tumour to be treated with
palliative appropriate modality (RT/CT/Sx )
 Adjuvants( Antidepressants, Anticonvulsants
biphosphonates, steroids, etc)used when required to
enhance efficacy of analgesia, treat concurrent
symptoms ,independent analgesic effect for specific type
of pain .
Reasons for Comprehensive pain
assesment
1.Pain expression influenced by factors:
Cognitive status
 Extreme of age
 Psychological reasons(fear of morphine related side
effects, progressive disease)
 Religious beliefs
 Communication barrier
2,Asses pain components: Bony
.Neuropathic
.Behavioral
.Somatic
3.Asses Comorbid conditions
(Renal,hepatic,Coagulopathy,GI,Respiratory)
Some Pain assesment scale
1.Numeric scale(0-10) based on patients own pain report
2. Rupee scale.
Children : Face scale  Happy to sad
2.Comprehensive pain evaluation:
By PQRST factor(Provocative, quality
, referred/regional
severity, temporal factors like onset ,duration ,frequency
etc.
 WHO designed simple, effective ,well validated
adjustment of pain therapy which results in pain relief in
90% cases, known as WHO pain ladder
 Some common analgesics proposed for use:
 NSAIDs-Aspirin, Ibuprofen , Naproxen , Piroxicam
, Celecoxib
 Weak Opioid-Codeine, dextropropoxyphine, Tramadol,
 Strong opioid-Morphine, buprenorphine, transdermal
Fentanyl
WHO LADDER OF
PAIN(cont.)
1-3
,NSAID+/-
Adjuvant
4-
6,WEAKOPI
OID,+/-
NONOPIOID
+/-
ADJUVANT
7-
10,STRONG
OPIOID=/-
NONOPIOID
+/-
ADJUVANT
Pharmacologic Management
 Drug therapy remains the cornerstone of cancer pain
management reasons being:
safe
Inexpensive
Works fast
Better compliance
3 major classes of drugs are:
 NSAIDS & Acetaminophen
 Opioid analgesics
 Adjuvant analgesic agents
Non Pharmacologic
Techniques
 Anesthetic - Local anesthetic
-Nerve block
 Neurosurgical techniques-Nerve ablation
-Nerve division
- Implant of device for
electrical stimulation
Physical methods-Heat ,cold, acupuncture , electrical
stimuli
.Cognitive techniques
1-15% cases requires invasive technique.
Morphine dose/side effects
 Inexpensive opioid given commonly by oral route
 Starting dose 10mg 4hrly,TDD usually 20-40mg , by
50% subsequently
 Parenteral dose 1/3rd of OD
 Breakthrough pain(10-15%) of daily dose.
 No max. dose.
 Extended release preparations when frequent dosing
required
Side effects requiring dose
modification ,adjuvants ,Switching
,alternate routes
 Constipation
 Sedation
 Myoclonus
 Opioid toxicity syndrome(OTS)-RF ,dehydration, severe
myoclonus
 Withdrawal symptoms
Infection in oncology
 Reason for significant morbidity & mortality
 Oncologist should have thorough understanding of risk
factors &common etiologic microbes
 Prompt work up & therapy are key to successful
management
Causes
  immunity-disease itself
-treatment induced neutropenia
.Protein malnutrition
Altered cellular/Humoral immunity
.Nosocomial
Post operative
.Secondary to obstruction & necrosis
.Exposure to community acquired pathogens(HSV,CMV)
.Reactivation of latent infections
Common Symptoms
 Fever
 Tachypnea
 Tachycardia
 Hypotension
 Hypothermia
 Organ specific
 Organ failure
 Routinely diagnosed by laboratory, microbial
,radiological tests
Guidelines for treatment
 Prompt initiation of broad spectrum antimicrobial empiric
monotherapy in suspected infections without waiting for
lab reports
 Directed therapy against specific pathogens as per
microbial culture report.
 In case β-lactam allergy fluoroquinolone based therapy
given.
 Diagnosis of febrile neutropenia should be done in
fever cases with ANC< 500/μl ,WBC <1000/μl.
 Documented bacteremia treated at least for 14 days.
Common pathogens
 S.aureus
 Enterococcus
 Pseudomonas
 C.difficle
 Klebsiella
 Proteus
 E.coli
 Candida
 Aspergillus
 CMV
Common Antimicrobials
 3rd /4th gen cephalosporins
 Carbapenems(Imepenem/Merpenem)
 Piperacillin-tazobactam
 Amoxycillin-clavulanate
 Fluoroquinolones
 Aztreonam
 Fluconazole
 Voriconazole
 Amphotericin-B
 Acyclovir
Thank you

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Chenai conf copy

  • 1. Guidelines of extravasation, infection &pain management in Oncology Dr. O.P. Singh M.D.FICRO. Prof & H.O.D (Radiotherapy) Gandhi Medical College Bhopal , India Dr. Gopa Ghosh M.D, Associate prof (Radiotherapy)S.S. Medical College Rewa ,India
  • 2. Extravasation can be defined as leakage of drug in to subcutaneous tissue which leads to either irritation or vescication.
  • 3. Classification of Cytotoxic drugs according to local site reaction 1.Irritan ts Inflamm ation,irr itation, Pain 2.Inflam mitants Inflamma tion/flare 3.Exfolia nts Shedding /Exfoliati on of skin ,no necrosis 4.Vescica nts Tissue Ulceratio n&necros is 5.Neutrals do not cause any damage
  • 4. Extravasation of a vescicant is a medical emergency hence calls for early detection &prompt action to prevent functional loss of limb involved.
  • 6. Probable risk factors for Peripheral Extravasation: Thin fragile veins Site of cannulation Peripheral neuropathy(Diabetes) Excessive movements due to altered mental status,vomitting,coughing SVC Syndrome Elderly/ Paediatric Obese Prior chemotherapy
  • 7. Cause of Central venous catheter leakage Backflow secondary to thrombosis in the catheter. Needle dislodgement from the port Damage of the catheter Thrombocytopenia
  • 8. Prevention of extravasation  Careful assesment of cannulation site  Cannulation over joints to be avoided  Patients at increased risk of extravasation should be identified.  Vescicant drugs to be given before other drugs  Bolus doses are given via fast running infusion of compatible fluid
  • 9. Continuous observation of cannulation site for signs of swelling ,pain inflammation, slowing of drip rate. Opinion for placement of CVAD should be sought if Peripheral access difficult. Extravastion can also occur in central access often of delayed onset .
  • 10. Signs/Symptom's Burning ,stinging ,pain at injection site Swelling ,redness , blister. Absence of free flow of infusion Resistance on the plunger of the syringe in case of bolus drug infusion No blood return in the cannula.
  • 11. Steps in management of extravasation Stop infusion ,disconnect tubing Withdraw as much as drug possible via existing cannula or CVAD Mark skin area with indelible pen Take photograph of the area Open extravasation kit Apply hot/cold pack as applicable for the concerned drug.
  • 12.  Elevate the limb  Inform treating oncologist  Urgent assesment by oncologist regarding referral to plastic surgeon for saline flush out of extravasated area.  Follow up at regular intervals.
  • 13. Contents of extravasation kit  Inj Hyaluronidase (1ampoule/1500iu)  Hydrocortisone 1%cream  S/w for injection  DMSO98%solution  Hot pack  Cold pack
  • 14. Drugs vs. Warm/Cold pack Vinca alkoids, Paclitax, Oxaloplatin Hyaluronidase+ Warm pack Anthracyclins,Mitoxantrone,Mitomycin,Dacti nomycinColdpack+DMSO+1%hudrocortis one cream Carboplat,Cisplat,Etoposide,5FU,Irrinotican, Mtx- Coldpack & Hydrocortisone cream
  • 15. Regime of Warm & Cold pack Warm 1amp Hyaluronidase s.c. inj  Warm pack to aid in absorption  Leave warm pack in situ for 2-4hrs Cold cold pack + Hydrocortison ecream 3days  Hydrocortisone 1%cream tds  OR Cold pack + hydrocortisone cream + DMSO
  • 16. DMSO application regime Thin layer 98% DMSO1%hydrocortisoneCold compress Rpt every2hr/24hrs  DMSO 6hrly7days  Alt toDMSO1% Hydrocortisone 6 hrly7days
  • 17. Cancer pain a matter of concern  60-80% of terminal cancer patients have severe pain  Moderate pain exists in earlier course of the disease also.  QOL of such patients are significantly impaired due to pain.  Chronic pain expressed in vague terms (stiffness ,anxiety ,insomnia), actual prevalance underestimated  85% cases can be pain free with modern drugs & techniques.
  • 18. Etiology 1. Direct infiltration to mucosa, soft tissues ,nerve &bone. 2.Treatment related (Sx/RT/CT) accounts for 20% pain cases.  Pain produced- stimulation of peripheral pain receptors.(nociceptive) Neurogenic/Neuropathic-( involvement of afferent nerves or nerve pathways.)
  • 19. Broad Principles of drug treatment Simplest dosage and least invasive route to be used first Analgesics to be given preferably around the clock basis than as need basis for more effective pain control. Opioid dose  till ultimate pain relief or unacceptable side effects. NAIDS &adjuvant analgesics with ceiling effect, dose till upper limit of recommended dose Switching of analgesics when required
  • 20.  Primary cause of pain i.e. tumour to be treated with palliative appropriate modality (RT/CT/Sx )  Adjuvants( Antidepressants, Anticonvulsants biphosphonates, steroids, etc)used when required to enhance efficacy of analgesia, treat concurrent symptoms ,independent analgesic effect for specific type of pain .
  • 21. Reasons for Comprehensive pain assesment 1.Pain expression influenced by factors: Cognitive status  Extreme of age  Psychological reasons(fear of morphine related side effects, progressive disease)  Religious beliefs  Communication barrier
  • 22. 2,Asses pain components: Bony .Neuropathic .Behavioral .Somatic 3.Asses Comorbid conditions (Renal,hepatic,Coagulopathy,GI,Respiratory)
  • 23. Some Pain assesment scale 1.Numeric scale(0-10) based on patients own pain report 2. Rupee scale. Children : Face scale  Happy to sad 2.Comprehensive pain evaluation: By PQRST factor(Provocative, quality , referred/regional severity, temporal factors like onset ,duration ,frequency etc.
  • 24.  WHO designed simple, effective ,well validated adjustment of pain therapy which results in pain relief in 90% cases, known as WHO pain ladder  Some common analgesics proposed for use:  NSAIDs-Aspirin, Ibuprofen , Naproxen , Piroxicam , Celecoxib  Weak Opioid-Codeine, dextropropoxyphine, Tramadol,  Strong opioid-Morphine, buprenorphine, transdermal Fentanyl
  • 26. Pharmacologic Management  Drug therapy remains the cornerstone of cancer pain management reasons being: safe Inexpensive Works fast Better compliance 3 major classes of drugs are:  NSAIDS & Acetaminophen  Opioid analgesics  Adjuvant analgesic agents
  • 27. Non Pharmacologic Techniques  Anesthetic - Local anesthetic -Nerve block  Neurosurgical techniques-Nerve ablation -Nerve division - Implant of device for electrical stimulation Physical methods-Heat ,cold, acupuncture , electrical stimuli .Cognitive techniques 1-15% cases requires invasive technique.
  • 28. Morphine dose/side effects  Inexpensive opioid given commonly by oral route  Starting dose 10mg 4hrly,TDD usually 20-40mg , by 50% subsequently  Parenteral dose 1/3rd of OD  Breakthrough pain(10-15%) of daily dose.  No max. dose.  Extended release preparations when frequent dosing required
  • 29. Side effects requiring dose modification ,adjuvants ,Switching ,alternate routes  Constipation  Sedation  Myoclonus  Opioid toxicity syndrome(OTS)-RF ,dehydration, severe myoclonus  Withdrawal symptoms
  • 30. Infection in oncology  Reason for significant morbidity & mortality  Oncologist should have thorough understanding of risk factors &common etiologic microbes  Prompt work up & therapy are key to successful management
  • 31. Causes   immunity-disease itself -treatment induced neutropenia .Protein malnutrition Altered cellular/Humoral immunity .Nosocomial Post operative .Secondary to obstruction & necrosis .Exposure to community acquired pathogens(HSV,CMV) .Reactivation of latent infections
  • 32. Common Symptoms  Fever  Tachypnea  Tachycardia  Hypotension  Hypothermia  Organ specific  Organ failure  Routinely diagnosed by laboratory, microbial ,radiological tests
  • 33. Guidelines for treatment  Prompt initiation of broad spectrum antimicrobial empiric monotherapy in suspected infections without waiting for lab reports  Directed therapy against specific pathogens as per microbial culture report.  In case β-lactam allergy fluoroquinolone based therapy given.  Diagnosis of febrile neutropenia should be done in fever cases with ANC< 500/μl ,WBC <1000/μl.  Documented bacteremia treated at least for 14 days.
  • 34. Common pathogens  S.aureus  Enterococcus  Pseudomonas  C.difficle  Klebsiella  Proteus  E.coli  Candida  Aspergillus  CMV
  • 35. Common Antimicrobials  3rd /4th gen cephalosporins  Carbapenems(Imepenem/Merpenem)  Piperacillin-tazobactam  Amoxycillin-clavulanate  Fluoroquinolones  Aztreonam  Fluconazole  Voriconazole  Amphotericin-B  Acyclovir