Kaushik.H.M
  080201388
 Rapid clinical assessment and resuscitation

 Detailed clinical assessment and species diagnosis

 Investigations/laboratory tests
 Specific treatment
 Attend to AIRWAY , BREATHING,
  CIRCULATION
 Secure an IV line (wide bore).
 Booster dose of tetanus toxoid is
  recommended.
 Identify the snake responsible
 All patients should be kept under
  observation for a minimum period of 24 hrs.
 Determine the exact time of bite
 Bacterial Infections- Prophylactic course of
 penicillin (or erythromycin for penicillin-
 hypersensitive patients)and a single dose of
 gentamicin or a course of chloramphenicol
•Care must be taken when removing tight tourniquets
tied by victim. Sudden removal can lead to massive
surge of venom leading to neurological paralysis,
hypotension.

•Pain-paracetamol/ 50 mg of tramadol maybe given.
NSAIDs and Aspirin are contraindicated.
Investigations
 20 minute whole blood clotting test -considered most
  reliable test of coagulation.
 Platelet count : may be decreased – viper

 WBC cell count : Early neutrophil leucocytosis in systemic
  envenoming from any species.

 Blood film : Fragmented RBC(“helmet cell”, schistocytes) are
  seen in microangiopathic haemolysis.

 Plasma/serum : may be pink or brownish if there is gross
  haemoglobinaemia or myoglobinaemia.
 Aminotransferases, creatine kinase, aldolase elevated if there
  is severe local damage or, particularly generalised muscle
  damage.

 Bilirubin is elevated following massive extravasation of blood.

 Creatinine, urea or blood urea nitrogen levels are raised in
  the renal failure

 Early hyperkalaemia may be seen following extensive
  rhabdomyolysis in sea snake bites. Bicarbonate will be low in
  metabolic acidosis (eg renal failure).

 Arterial blood gases and pH may show evidence of respiratory
  failure (neurotoxic envenoming) and acidaemia (respiratory
  or metabolic acidosis).
 Urine for RBC – Viper Bite – Hematuria,
  Proteinuria, Hemoglobinuria, Myoglobinuria

 ECG – Normal, Bradycardia with ST elevation or
  depression, T inversion, QT prolongation.

 Chest X- ray – Normal or may show Pulmonary
  Oedema, Intrapulmonary Hemorhages, Pleural
  Effusion.
Monitor vital signs
 Observe every patient for minimum 24 hours. Monitor the
patient every 6 hours.
 Pulse, BP, Respiration
 Urine output
 Blood urea, Creatinine
 Bleeding tendency
 Local swelling
 Vomiting
 Diplopia, Ptosis, Muscle Weakness, Breathlessness
Anti Snake Venom
 Antivenom is immunoglobulin (usually the enzyme
  refined F(ab)2 fragment of IgG) purified from the
  serum or plasma of a horse or sheep that has been
  immunised with the venoms of one or more species of
  snake.
 It neutralises the free, unbound venom & to some
  extent also dissociates the bound toxin
 ASV is manufactured in India by the Haffkine Central
  Research Institute, Kasauli & Serum Institute of India,
  Pune & both are POLYVALENT(neutralizes venom of
  different species of snakes.)
1 ml of ASV neutralises
 Cobra – 0.6 mg
 Common krait – 0.45mg
 Russels viper – 0.6 mg
 Saw scaled viper – 0.45 mg
Indications
 As per W.H.O Guidelines ONLY if a patient
  develops one / more of the following
  signs/symptoms ASV should be administered :
SYSTEMIC ENVENOMING
• Evidence of coagulopathy: detected by
  20WBCT or visible spontaneous systemic
  bleeding
• Evidence of neurotoxicity : ptosis,
  ext.ophthalmoplegia
• CVS abnormalities : hypotension, shock,
 arrhythmias

• Acute renal failure

• Hemoglobinuria / myoglobinuria

• Persistent severe vomiting / abdominal pain
LOCAL ENVENOMING
• Local swelling > ½ of involved limb


• Rapid extension of swelling


• Enlarged tender lymph nodes draining the bitten limb
ASV administration
 NO ASV TEST DOSE MUST BE ADMINISTERED .


 Recommended initial dosages are 100 ml( 10 vials) of
  polyvalent ASV for adults & children          based on
  published research that russells viper injects on an
  average of 63 mg of venom.

 Our initial dose must be calculated to neutralize the
 average dose of venom injected.
 Range of venom injected = 5mg – 147 mg


 Suggested ASV dose = 100 -250 ml


 Initial dose of 100 ml must be diluted in 100 ml of NS &
 given over 1 hour.

 Patient should be carefully monitored for 2 hrs.


 Local administration of ASV, near the bite site –
 ineffective, painful, raises intracompartmental pressure.
 – SHOULD NOT BE DONE
Victim who arrives late ?
 Often after several days , usually with acute renal failure.


 Are there any signs of current venom activity ?


 Perform 20WBCT & determine if any coagulopathy is
  +, if + administer ASV. If - , treat ARF – dialysis

 Neurotoxic envenoming – look for ptosis, respiratory
  failure , + administer 1 dose of ASV , respiratory support
ASV reactions
 Patient should be monitored closely

 First sign of any one of the following :
  1. Utricaria 6. Vomiting 11.Bronchospasm
  2. Itching      7. Diarrhoea 12.Angioedema
 3. Fever     8. Abdominal cramps
 4. Chills     9. Tachycardia
 5. Nausea    10. Hypotension

 Discontinue ASV & give 0.5 mg of 1 :1000 adrenaline
  IM/ IV diphenhydramine(antihistamines).
Repeat doses of ASV
 HEMATOTOXIC POISONING :

• 20 WBCT – abnormal – initial dose given over 1 hr.

• Repeat 20WBCT after 6 hrs

• Abnormal – another dose to be given. Repeat same
  dose again.

• 20WBCT & Repeat doses of ASV – to be continued
  on 6 hourly manner until coagulation is restored.
 NEUROTOXIC POISONING

• Assess the patient 1-2 hrs after the initial dose


• If symptoms persist / worsen , 2 nd dose which is
 same as 1st dose is to be given & then ASV can be
 discontinued
Role of Neostigmine in
Neurotoxic poisoning
 Anticholinestrase & prolongs life of Ach - which can
    reverse resp.failure & neurotoxic symptoms ( post synaptic
    )
   Neostigmine test : 1.5 -2.0 mg IM preceeded by 0.6 mg
    atropine IV
•   Observe for 1 hr
•   If victim responds , continue 0.5 mg Neostigmine IM ½
    hrly with 0.6 mg Atropine IV over 8 hrs
•   If no improvement in symptoms after 1 hr , stop
    Neostigmine
Supportive Therapy
 RESPIRATORY FAILURE :
• ABG
• Intubate & Ventilate
• Neostigmine & Atropine


 HYPOTENSION :
• Plasma expanders-crystalloids
• Dopamine 2.5 – 5 micrograms/Kg/min
 PERSISTANT / SEVERE BLEEDING :
• Majority – timely use of ASV will stop systemic bleed
• ASV + Blood Transfusion

 RENAL FAILURE
• Hemodialysis / peritoneal dialysis

 COMPARTMENT SYNDROME :
• Fasciotomy

 SURGICAL DEBRIDEMENT OF WOUND: Necrosis

Treatment protocol of snake bite

  • 1.
  • 2.
     Rapid clinicalassessment and resuscitation  Detailed clinical assessment and species diagnosis  Investigations/laboratory tests  Specific treatment
  • 3.
     Attend toAIRWAY , BREATHING, CIRCULATION  Secure an IV line (wide bore).  Booster dose of tetanus toxoid is recommended.  Identify the snake responsible
  • 4.
     All patientsshould be kept under observation for a minimum period of 24 hrs.  Determine the exact time of bite  Bacterial Infections- Prophylactic course of penicillin (or erythromycin for penicillin- hypersensitive patients)and a single dose of gentamicin or a course of chloramphenicol
  • 5.
    •Care must betaken when removing tight tourniquets tied by victim. Sudden removal can lead to massive surge of venom leading to neurological paralysis, hypotension. •Pain-paracetamol/ 50 mg of tramadol maybe given. NSAIDs and Aspirin are contraindicated.
  • 6.
    Investigations  20 minutewhole blood clotting test -considered most reliable test of coagulation.  Platelet count : may be decreased – viper  WBC cell count : Early neutrophil leucocytosis in systemic envenoming from any species.  Blood film : Fragmented RBC(“helmet cell”, schistocytes) are seen in microangiopathic haemolysis.  Plasma/serum : may be pink or brownish if there is gross haemoglobinaemia or myoglobinaemia.
  • 7.
     Aminotransferases, creatinekinase, aldolase elevated if there is severe local damage or, particularly generalised muscle damage.  Bilirubin is elevated following massive extravasation of blood.  Creatinine, urea or blood urea nitrogen levels are raised in the renal failure  Early hyperkalaemia may be seen following extensive rhabdomyolysis in sea snake bites. Bicarbonate will be low in metabolic acidosis (eg renal failure).  Arterial blood gases and pH may show evidence of respiratory failure (neurotoxic envenoming) and acidaemia (respiratory or metabolic acidosis).
  • 8.
     Urine forRBC – Viper Bite – Hematuria, Proteinuria, Hemoglobinuria, Myoglobinuria  ECG – Normal, Bradycardia with ST elevation or depression, T inversion, QT prolongation.  Chest X- ray – Normal or may show Pulmonary Oedema, Intrapulmonary Hemorhages, Pleural Effusion.
  • 9.
    Monitor vital signs Observe every patient for minimum 24 hours. Monitor the patient every 6 hours.  Pulse, BP, Respiration  Urine output  Blood urea, Creatinine  Bleeding tendency  Local swelling  Vomiting  Diplopia, Ptosis, Muscle Weakness, Breathlessness
  • 10.
    Anti Snake Venom Antivenom is immunoglobulin (usually the enzyme refined F(ab)2 fragment of IgG) purified from the serum or plasma of a horse or sheep that has been immunised with the venoms of one or more species of snake.  It neutralises the free, unbound venom & to some extent also dissociates the bound toxin  ASV is manufactured in India by the Haffkine Central Research Institute, Kasauli & Serum Institute of India, Pune & both are POLYVALENT(neutralizes venom of different species of snakes.)
  • 11.
    1 ml ofASV neutralises  Cobra – 0.6 mg  Common krait – 0.45mg  Russels viper – 0.6 mg  Saw scaled viper – 0.45 mg
  • 12.
    Indications  As perW.H.O Guidelines ONLY if a patient develops one / more of the following signs/symptoms ASV should be administered : SYSTEMIC ENVENOMING • Evidence of coagulopathy: detected by 20WBCT or visible spontaneous systemic bleeding • Evidence of neurotoxicity : ptosis, ext.ophthalmoplegia
  • 13.
    • CVS abnormalities: hypotension, shock, arrhythmias • Acute renal failure • Hemoglobinuria / myoglobinuria • Persistent severe vomiting / abdominal pain
  • 14.
    LOCAL ENVENOMING • Localswelling > ½ of involved limb • Rapid extension of swelling • Enlarged tender lymph nodes draining the bitten limb
  • 15.
    ASV administration  NOASV TEST DOSE MUST BE ADMINISTERED .  Recommended initial dosages are 100 ml( 10 vials) of polyvalent ASV for adults & children based on published research that russells viper injects on an average of 63 mg of venom.  Our initial dose must be calculated to neutralize the average dose of venom injected.
  • 16.
     Range ofvenom injected = 5mg – 147 mg  Suggested ASV dose = 100 -250 ml  Initial dose of 100 ml must be diluted in 100 ml of NS & given over 1 hour.  Patient should be carefully monitored for 2 hrs.  Local administration of ASV, near the bite site – ineffective, painful, raises intracompartmental pressure. – SHOULD NOT BE DONE
  • 17.
    Victim who arriveslate ?  Often after several days , usually with acute renal failure.  Are there any signs of current venom activity ?  Perform 20WBCT & determine if any coagulopathy is +, if + administer ASV. If - , treat ARF – dialysis  Neurotoxic envenoming – look for ptosis, respiratory failure , + administer 1 dose of ASV , respiratory support
  • 18.
    ASV reactions  Patientshould be monitored closely  First sign of any one of the following : 1. Utricaria 6. Vomiting 11.Bronchospasm 2. Itching 7. Diarrhoea 12.Angioedema 3. Fever 8. Abdominal cramps 4. Chills 9. Tachycardia 5. Nausea 10. Hypotension  Discontinue ASV & give 0.5 mg of 1 :1000 adrenaline IM/ IV diphenhydramine(antihistamines).
  • 19.
    Repeat doses ofASV  HEMATOTOXIC POISONING : • 20 WBCT – abnormal – initial dose given over 1 hr. • Repeat 20WBCT after 6 hrs • Abnormal – another dose to be given. Repeat same dose again. • 20WBCT & Repeat doses of ASV – to be continued on 6 hourly manner until coagulation is restored.
  • 20.
     NEUROTOXIC POISONING •Assess the patient 1-2 hrs after the initial dose • If symptoms persist / worsen , 2 nd dose which is same as 1st dose is to be given & then ASV can be discontinued
  • 21.
    Role of Neostigminein Neurotoxic poisoning  Anticholinestrase & prolongs life of Ach - which can reverse resp.failure & neurotoxic symptoms ( post synaptic )  Neostigmine test : 1.5 -2.0 mg IM preceeded by 0.6 mg atropine IV • Observe for 1 hr • If victim responds , continue 0.5 mg Neostigmine IM ½ hrly with 0.6 mg Atropine IV over 8 hrs • If no improvement in symptoms after 1 hr , stop Neostigmine
  • 22.
    Supportive Therapy  RESPIRATORYFAILURE : • ABG • Intubate & Ventilate • Neostigmine & Atropine  HYPOTENSION : • Plasma expanders-crystalloids • Dopamine 2.5 – 5 micrograms/Kg/min
  • 23.
     PERSISTANT /SEVERE BLEEDING : • Majority – timely use of ASV will stop systemic bleed • ASV + Blood Transfusion  RENAL FAILURE • Hemodialysis / peritoneal dialysis  COMPARTMENT SYNDROME : • Fasciotomy  SURGICAL DEBRIDEMENT OF WOUND: Necrosis