Explain in detail icmr guidelines on snake bite

Reading File
Searching the Web

ICMR guidelines snakebite management India 2024 2025

Finding Sources
Reading Web Page

ICMR snakebite management guidelines antivenom treatment

Finding Sources
Reading Web Page

ICMR snakebite guidelines antivenom dose indications 20WBCT neurotoxic hemotoxic

I now have comprehensive content from the Indian guidelines. Let me compile a thorough, detailed response.

ICMR / NHM Guidelines on Snakebite Management in India

India follows the National Health Mission (NHM) Standard Treatment Guidelines (STG) for Snakebite Management (Ver. 4.0), developed in collaboration with ICMR, WHO Country Office India, and a multidisciplinary expert group. These are pan-India, evidence-based guidelines adapted to the Indian epidemiological context. Below is a detailed walkthrough of every major section.

1. Epidemiological Context

India accounts for a disproportionate share of global snakebite deaths. The "Big Four" medically important snakes in India are:
  • Indian Cobra (Naja naja) - neurotoxic + cytotoxic
  • Common Krait (Bungarus caeruleus) - neurotoxic (presynaptic)
  • Russell's Viper (Daboia russelii) - hemotoxic + nephrotoxic
  • Saw-scaled Viper (Echis carinatus) - hemotoxic + coagulopathic
Outcome depends on: species, size of snake, time of day (nocturnal kraits), delay to treatment, and dose of venom injected. A significant proportion of bites are "dry bites" with no envenomation.

2. Stages of Management

The guidelines define a structured stepwise approach:
  1. First aid at scene
  2. Transport to hospital
  3. Rapid clinical assessment and resuscitation
  4. Investigations / laboratory tests
  5. Species diagnosis (clinical or by snake identification)
  6. Antivenom (ASV) treatment
  7. Observing response to ASV
  8. Deciding on further ASV doses
  9. Supportive/ancillary treatment
  10. Treatment of the bitten part
  11. Rehabilitation and follow-up

3. First Aid - What to DO

These are to be performed by bystanders or the victim themselves before reaching a hospital:
  • Reassure the victim - death is not imminent, medical care is available
  • Control anxiety - anxiety increases heart rate and accelerates venom absorption
  • Position: Lay the victim flat, bitten limb below heart level to slow lymphatic spread
  • Remove rings, watches, shoes, and tight clothing from the bitten area (to prevent tourniquet effect when swelling develops)
  • Immobilize the bitten limb using a splint and light bandage (similar to fracture immobilization)
  • Pressure Pad: There is some preliminary evidence for a "pressure pad" at bite site - but this needs further field evaluation in India and is not yet firmly recommended
  • Transport immediately to the nearest secondary or tertiary care hospital with antivenom availability
  • The victim must not run or drive himself - use vehicle/ambulance (102/108), boat, bicycle, motorbike, or stretcher

4. First Aid - What NOT to Do

The guidelines are very explicit about harmful practices to avoid:
Harmful PracticeWhy It Is Harmful
Apply tourniquetCauses ischemia, necrosis; sudden removal causes venom surge
Wash bite site with soap/solutionsDoes not remove venom effectively
Cut/incise near the biteIncreases bleeding, infection risk
Electrical shockNo benefit, harmful
Freeze or apply extreme coldCauses frostbite/necrosis
Herbal/folk remediesNo proven benefit, cause dangerous delays
Suck out venom orallyIneffective and dangerous to the rescuer
Give alcohol or other drugsMasks symptoms, harmful
Try to capture/kill the snakeRisk of another bite
Take to quacksLethal delay in reaching definitive care

5. Clinical Assessment on Arrival

Systemic Envenomation Signs

Neurotoxic (Cobra, Krait):
  • Ptosis (drooping eyelids) - earliest sign
  • Blurred vision, diplopia
  • Difficulty swallowing, drooling
  • Slurred speech
  • Weakness of limbs
  • Respiratory paralysis (life-threatening)
Hemotoxic/Coagulopathic (Russell's Viper, Saw-scaled Viper):
  • Spontaneous bleeding (gums, sites of venepuncture, haematuria)
  • Swelling and bruising
  • Blood in urine
  • Acute Kidney Injury (Russell's Viper in particular)
Local Signs (primarily Viper bites):
  • Pain and swelling within minutes
  • Blistering, necrosis
  • Lymphadenopathy

6. Investigations

20-Minute Whole Blood Clotting Test (20WBCT) - Key Bedside Test

The 20WBCT is the cornerstone investigation, particularly valuable in resource-limited settings:
  • Place a few mL of fresh venous blood in a clean, dry glass test tube (NOT plastic)
  • Leave undisturbed at ambient temperature for 20 minutes
  • Gently tilt the tube - if blood is still liquid (no clot), it is incoagulable - indicates viper envenomation
  • Perform every 30 minutes from admission for the first 3 hours, then hourly
  • If neurotoxic snake bite is confirmed, repeat at 6 hours
The 20WBCT is considered superior to the capillary tube method for establishing coagulation status.

Other Investigations

  • CBC, coagulation profile (PT/INR, aPTT), fibrinogen
  • Renal function tests (urea, creatinine) - especially Russell's Viper
  • Urine examination (for haematuria, haemoglobinuria)
  • Arterial blood gas (for respiratory failure in neurotoxic envenomation)
  • Note: Arterial puncture is contraindicated in patients with haemostatic abnormalities

7. Anti-Snake Venom (ASV) - Core Treatment

Indications for ASV

ASV should be given when any of the following are present:
  • Signs of systemic envenomation (neurotoxic OR hemotoxic)
  • 20WBCT showing incoagulable blood
  • Spontaneous bleeding
  • Ptosis, respiratory failure, or neurotoxic signs
  • Local envenomation with rapidly spreading swelling

ASV Test Dose

  • NOT recommended - test doses have not been shown to have predictive value in preventing anaphylaxis or serum sickness
  • Adrenaline must always be drawn up and ready (0.5 mg IM in two syringes) before starting ASV

ASV Dosage (Indian Guidelines)

SituationDose
Mild envenomation (systemic symptoms appear >3 hours after bite)8-10 vials
Severe envenomation (systemic symptoms appear <3 hours after bite)8 vials (same for hemotoxic or neurotoxic)
  • Each vial = 10 mL of reconstituted polyvalent ASV
  • Children receive the same dose as adults (the venom dose does not vary by body weight)
  • ASV is given intravenously (IV infusion preferred over IV push)

Repeat Doses of ASV

For Hemotoxic (Viper) envenomation:
  • After the initial dose, no additional ASV until the next 20WBCT at 6 hours (the liver cannot replace clotting factors in less than 6 hours)
  • If 20WBCT still incoagulable at 6 hours: give 5-10 vials (half to full dose)
  • Continue 6-hourly until coagulation is restored or species identified as one against which polyvalent ASV is ineffective
For Neurotoxic (Cobra/Krait) envenomation:
  • Reassess at 1-2 hours after initial dose
  • If symptoms worsened or not improved: give a second dose of 10 vials, then discontinue
  • Once patient develops respiratory failure AND has received 20 vials total: discontinue ASV (assume all circulating venom is neutralized) and initiate assisted ventilation
  • Exception: King Cobra and Australian elapids may require 50+ vials due to large venom loads

Late Presentations (Patients Arriving Days After Bite)

A common scenario in India - patient arrives with acute renal failure several days after bite:
  • Key principle: ASV can only neutralize unbound/circulating venom
  • Perform 20WBCT - if coagulopathy is still present, give ASV
  • For neurotoxic envenomation with ongoing ptosis/respiratory failure: give 1 dose of 8-10 vials (to clear any residual unbound venom), then provide respiratory support

8. ASV Reactions and Their Management

Early Reactions (Anaphylaxis/Anaphylactoid)

Occur within 30-60 minutes of starting ASV. Signs: urticaria, pruritus, fever, chills, hypotension, bronchospasm.
Management:
  • Temporarily suspend ASV infusion
  • Give Adrenaline 0.25-0.3 mg subcutaneously (IM preferred)
  • Once reaction controlled, recommence ASV at a slower rate
  • Pre-treatment with subcutaneous adrenaline 0.25 mg may reduce risk in high-risk patients

Pyrogenic (Febrile) Reactions

Occur 1-2 hours after ASV, caused by pyrogens in the ASV preparation. Manage with antipyretics.

Late Serum Sickness

Occurs 5-10 days later: fever, urticaria, arthralgia, lymphadenopathy. Managed with oral antihistamines and a short course of corticosteroids.

9. Specific Antidotes and Adjunct Treatments

Neostigmine (for Cobra bites - postsynaptic neurotoxins)

  • Neostigmine Test: Administer 0.5-2 mg IV neostigmine
  • If neurological improvement occurs (ptosis improves, muscle strength returns), continue neostigmine every 30 minutes over the next 8 hours along with atropine
  • Effective only against postsynaptic neurotoxins (Cobra)
  • NOT effective against presynaptic neurotoxins (Common Krait, Russell's Viper)

Pain Management

  • Paracetamol (acetaminophen): Adults 500 mg to 1 g orally; Children 10-15 mg/kg/dose (max 100 mg/kg/day)
  • Do NOT give Aspirin or NSAIDs - risk of bleeding and renal dysfunction

Tetanus Prophylaxis

  • Administer tetanus toxoid if the skin is breached

Medications NOT to Use

  • Heparin: Ineffective against venom-induced thrombin consumption; may worsen bleeding - never use
  • Botropase (haemocoagulase): Not recommended
  • Antifibrinolytics (tranexamic acid): Not effective in VICC (venom-induced consumption coagulopathy)
  • Steroids: Not routinely recommended
  • Antihistamines as prophylaxis for ASV reactions: Evidence is weak

10. Tourniquet Management

Although tourniquets are strongly contraindicated, patients frequently arrive with tight tourniquets applied at the scene:
  • Do NOT suddenly remove a tight tourniquet - sudden removal can cause a massive surge of venom into systemic circulation
  • Loosen tourniquet gradually while monitoring the patient closely
  • Ensure IV access and resuscitation equipment is ready before loosening

11. Management at Different Levels of Healthcare

Primary Health Centre (PHC)

  • First aid, supportive care
  • 20WBCT
  • If ASV available and staff trained: administer first dose of ASV
  • If not: stabilize and transfer immediately
  • Oxygen, IV fluids for shock
  • If respiratory paralysis: oxygen by mask/LMA, Ambu bag, arrange urgent transfer with Medical Officer escort

Community / Dispensary Level

  • Basic first aid
  • Identify need for transfer
  • Do NOT attempt ASV if skills/equipment not available

Secondary and Tertiary Care

  • Full management including ICU care, dialysis (for Russell's Viper-induced AKI), mechanical ventilation, surgical wound management

12. Special Situations

Pregnancy

  • ASV is not contraindicated in pregnancy
  • Benefit of treating envenomation outweighs risk
  • Monitor fetal well-being

Venom-Induced Consumption Coagulopathy (VICC)

  • Caused by procoagulant toxins (mainly Russell's Viper, Saw-scaled Viper) consuming clotting factors
  • Response to ASV may require multiple 6-hourly doses
  • Fresh Frozen Plasma (FFP) or blood products may be needed for life-threatening bleeding, but only after adequate ASV

Acute Kidney Injury (Russell's Viper)

  • Most common complication of Russell's Viper bite in India
  • Monitor urine output, creatinine
  • Early dialysis if required
  • ASV should still be given if coagulopathy is present

13. Follow-Up and Rehabilitation

  • Patients should be followed up for late serum sickness (5-10 days post-ASV)
  • Monitor renal function in Russell's Viper bites for weeks to months
  • Wound care and physiotherapy for local necrosis/tissue loss
  • Psychological support for patients who develop PTSD

14. Prevention (Community Level)

The guidelines emphasize prevention as the most effective strategy:
  • Wear boots and protective clothing in fields
  • Use torches at night
  • Sleep off the ground (kraits are nocturnal ground-level predators)
  • Clear undergrowth and debris around homes
  • Community health education through media, role-play, FM radio, mobile messaging
  • Display snakebite protocol posters in hospital waiting areas
  • Avoid handling or trying to catch/kill snakes

Key Summary Table

ParameterRecommendation
First-line bedside test20WBCT (glass tube, 20 minutes)
ASV dose (mild)8-10 vials IV
ASV dose (severe)8 vials IV (same for neurotoxic/hemotoxic)
Child vs adult ASV doseSame dose
ASV test doseNot recommended
Pre-ASV drugAdrenaline 0.5 mg drawn up ready
NeostigmineUseful for Cobra (postsynaptic); useless for Krait
Repeat ASV interval6-hourly (hemotoxic); 1-2 hourly reassessment (neurotoxic)
Max ASV for neurotoxic20 vials, then switch to ventilatory support
HeparinAbsolutely contraindicated
Aspirin/NSAIDsContraindicated
TourniquetContraindicated; if present, remove gradually
Anaphylaxis treatmentAdrenaline 0.25-0.3 mg SC/IM, temporarily suspend ASV

Source: NHM Standard Treatment Guidelines - Management of Snakebite (Full Background Document, Ver. 4.0), developed in collaboration with ICMR, WHO Country Office India, NHSRC. Also based on the Indian Guidelines and Protocol document from SCTIMST (Sree Chitra Tirunal Institute for Medical Sciences and Technology). The NHM guidelines are available here.
Note: These guidelines are reviewed every 3 years or whenever there is a major therapeutic breakthrough. Always check the latest NHM/ICMR portal for the most current version.

How to give asv in adult and children and how to constitute adr in shock and anaphylaxis AND DOSE

Searching the Web

ICMR NHM India ASV anti snake venom administration dose adults children constitution anaphylaxis adrenaline

Finding Sources
Reading Web Page

ASV constitution reconstitution administration dose adults children adrenaline anaphylaxis shock infusion rate

Excellent - I have all the specific details. Here is a complete, clinical breakdown:

ASV Administration and Adrenaline Dosing - ICMR / NHM Guidelines


PART 1: How to Constitute and Give ASV

Types of ASV Available in India

TypeShelf LifeCold ChainReconstitution Time
Liquid ASV2 yearsRequires refrigerationImmediate (ready to use)
Lyophilised ASV (powder)5 yearsOnly needs to be kept cool (no strict cold chain)30-60 minutes to reconstitute
Lyophilised ASV is preferred for remote/rural areas where power supply is unreliable.

Step-by-Step Constitution of ASV

Lyophilised (Powder) ASV

  1. Add sterile water for injection (distilled water) into the vial per manufacturer instructions
  2. Gently swirl (do NOT shake) until powder is fully dissolved
  3. Reconstitution takes 30-60 minutes - plan ahead
  4. Once reconstituted, treat like liquid ASV

Dilution for Infusion

  • Dissolve 10 vials of ASV in 100 mL of distilled water first
  • Then add this to 400 mL of Normal Saline (0.9% NaCl) = total 500 mL
  • In children: Dilute in 5-10 mL/kg body weight of Normal Saline; reduce the volume in the running bottle to 200 mL maximum to avoid fluid overload

Route of Administration

  • IV route ONLY - ASV must never be given IM or SC (except the small prophylactic adrenaline dose described below)
  • The physician must be at the bedside during the initial period of infusion to intervene immediately at the first sign of reaction

Infusion Rate

  • Start slowly
  • Observe the patient every 5 minutes for the first 30 minutes, then every 15 minutes for the next 2 hours
  • Increase the infusion rate gradually in the absence of a reaction
  • Target: full starting dose administered over approximately 1 hour
  • At the earliest sign of any adverse reaction - suspend immediately

ASV Dose

Adults

Clinical SituationDose
Mild envenomation (systemic symptoms appear >3 hours after bite)8-10 vials IV
Severe envenomation (systemic symptoms appear <3 hours after bite)8 vials IV

Children

Children receive the EXACT SAME dose as adults. This is because snakes inject the same amount of venom regardless of the victim's body weight. Do NOT reduce the dose.
Clinical SituationDose
Mild envenomation8-10 vials IV (same as adult)
Severe envenomation8 vials IV (same as adult)
Infusion volumeDilute in 5-10 mL/kg of NS, max 200 mL in the running bottle

Pregnancy

  • Same dose as adults, no reduction. Refer to gynecologist for fetal monitoring.

Repeat Doses

Envenomation TypeWhen to RepeatDose
Hemotoxic (Viper)If 20WBCT still incoagulable at 6 hours5-10 vials; repeat 6-hourly until coagulation restored
Neurotoxic (Cobra/Krait)Reassess at 1-2 hours after initial dose; if no improvement or worseningSecond dose of 10 vials, then STOP
Neurotoxic maxAfter 20 total vials receivedStop ASV, switch to mechanical ventilation

ASV Test Dose

  • NOT recommended - test doses do NOT predict anaphylaxis and are not given per Indian guidelines

PART 2: Prophylactic Adrenaline BEFORE Starting ASV

The NHM/NCDC guidelines recommend routine prophylactic (preemptive) adrenaline before ASV infusion - except in:
  • Known hypertensive patients
  • BP >140/90 mmHg on arrival
  • Suspected or known underlying cardiovascular disease
PatientProphylactic Adrenaline DoseRoute
Adult0.25 mg (0.25 mL) of 1:1000 solutionSubcutaneous (SC) - just before adding ASV to the running IV fluid
Child0.005 mg/kg of 0.1% (1:1000) solutionSubcutaneous
Additionally: Draw up two syringes of adrenaline (0.5 mg each) and keep them ready at the bedside before starting any ASV infusion.

PART 3: Treatment of EARLY ASV Reaction (Anaphylaxis / Anaphylactoid)

When Does It Happen?

  • Within 30-60 minutes of starting ASV
  • Signs: urticaria (even a single patch), itching, restlessness, vomiting, hot/cold feeling, sudden dry cough, abdominal pain, dyspnoea, fall in BP, facial swelling, angioedema, tongue protrusion

Step-by-Step Management

Step 1 - STOP ASV immediately at the FIRST sign (even just a single patch of urticaria or itching)
Step 2 - Oxygen - give high-flow oxygen by mask
Step 3 - Start fresh IV Normal Saline with a NEW IV set
Step 4 - ADRENALINE (drug of choice)
PatientDoseConcentrationRouteSite
Adult0.5 mg (0.5 mL)1:1000 (1 mg/mL) solutionIntramuscular (IM)Deltoid muscle or outer thigh
Child0.01 mg/kg body weight1:1000 solutionIntramuscular (IM)Outer thigh preferred
Why IM over SC? - IM gives faster peak adrenaline levels (8 minutes to peak vs longer for SC). The deltoid (or vastus lateralis in children) is the recommended injection site. Speed is critical - the faster adrenaline is given, the sooner ASV can be restarted.
Step 5 - Chlorpheniramine maleate (antihistamine)
PatientDoseRoute
Adult10 mgIV
Child0.2 mg/kgIV
Step 6 - Hydrocortisone - can be given but unlikely to act for several hours; it is NOT the primary drug for anaphylaxis
Step 7 - RESTART ASV once patient has recovered - restart slowly for the first 10-15 minutes under close observation, then resume normal drip rate

PART 4: Treatment of ANAPHYLACTIC SHOCK

When the reaction progresses to frank shock (hypotension, loss of consciousness, cardiovascular collapse):

Adrenaline Dose in Shock

PatientDoseRouteConcentration
Adult0.5 mg IM (repeat every 5 minutes if needed)IM - deltoid/thigh1:1000
Child0.01 mg/kg IM (repeat every 5 minutes if needed)IM - outer thigh1:1000
For refractory shock not responding to IM adrenaline:
PatientDoseRoutePreparation
Adult0.1 mg IV slowly (titrated) OR infusion at 0.1-1 mcg/kg/minIVDilute 1 mL of 1:1000 adrenaline to 10 mL with NS = 1:10,000 = 0.1 mg/mL; give 1 mL slowly IV
Child0.01 mg/kg IV OR infusion at 0.1-1 mcg/kg/minIVSame dilution principle
The Bhutan National Guideline (adopted from WHO/India protocol) provides a specific infusion chart: See annexure for adrenaline infusion dosing by weight.

Full Resuscitation in Shock

  1. Large-bore IV access, rapid IV fluid bolus (Normal Saline 20 mL/kg over 20 min in children; 500-1000 mL in adults)
  2. Lay flat, elevate legs
  3. Adrenaline IM (first line) or IV infusion (if refractory)
  4. Oxygen / airway management
  5. Call for ICU/anaesthesia support for intubation if airway is compromised

PART 5: High-Risk Patients - Special Protocol Before ASV

For patients with history of hypersensitivity to horse/animal serum (prior ASV, rabies immunoglobulin, tetanus antitoxin) or severe atopic disease:
  • Give ASV only if systemic envenomation is confirmed (not for dry bites)
  • Pre-medicate with:
    • Inj. Hydrocortisone 200 mg IV AND
    • Inj. Chlorpheniramine maleate 22.75 mg IV

PART 6: Desensitization (Only for Severe Refractory Anaphylaxis)

Used only when: severe anaphylaxis with shock + generalized anasarca occurs after injection of very few mL (<5 mL) of diluted ASV, AND ASV is life-saving and must continue.
Table 1 - Steps of Dilution for Desensitization:
StepInstructionsDilution
1Dilute ASV 1:10 in NSVery dilute
2Gradually increase concentration1:5, then 1:2
3Full concentrationUndiluted
  • Pre-medicate: Hydrocortisone 100 mg IV + Adrenaline 0.5 mL SC/IM (± Promethazine)
  • Change the batch of ASV if available

PART 7: Late Serum Sickness (5-12 days after ASV)

Features: fever, urticaria, arthralgia, myalgia, lymphadenopathy, immune complex nephritis, rarely encephalopathy
DrugAdult DoseChild DoseDuration
Chlorpheniramine2 mg 6-hourly0.25 mg/kg/day5 days
Prednisolone (if no response in 24-48 h)5 mg 6-hourly0.7 mg/kg/day in divided doses5 days

Quick Reference Cheat Sheet

ASV INFUSION
- Dilute: 10 vials in 100 mL DW → add to 400 mL NS = 500 mL total
- Children: 5-10 mL/kg NS, max 200 mL in bottle
- Rate: Slowly over ~1 hour, physician at bedside
- Dose: SAME for adults and children (8-10 vials mild; 8 vials severe)

PROPHYLACTIC ADRENALINE (before ASV)
- Adult: 0.25 mg SC of 1:1000
- Child: 0.005 mg/kg SC of 1:1000
- SKIP if: hypertensive, BP >140/90, CVD

ANAPHYLAXIS TREATMENT (adrenaline)
- Adult: 0.5 mg IM (0.5 mL of 1:1000) - deltoid/thigh
- Child: 0.01 mg/kg IM - outer thigh
- Repeat every 5 min if needed
- Refractory shock: IV adrenaline infusion 0.1-1 mcg/kg/min

CHLORPHENIRAMINE (with adrenaline)
- Adult: 10 mg IV
- Child: 0.2 mg/kg IV

RESTART ASV after reaction settled: slowly for 10-15 min, then normal rate

Give management with doses and timing of op poisoning. Morphine poisoning, paraquat poisoning, myocardial infarction, dyslipidemia, hypertriglycerdimia, at phc and chc level also how to manage acute abdomen at phc level and diff rent dd

Searching the Web

ICMR NHM India OP organophosphate poisoning management atropine pralidoxime dose PHC CHC guidelines

Finding Sources
Searching the Web

NHM India STG myocardial infarction dyslipidemia paraquat poisoning morphine opioid poisoning management doses PHC level

Finding Sources
Reading Web Page

OP poisoning atropine pralidoxime dose timing PHC CHC management protocol India

Searching the Web

paraquat poisoning management treatment protocol India NHM standard treatment guidelines acute abdomen PHC differential diagnosis

Reading Web Page

organophosphate OP poisoning atropine pralidoxime dose timing management PHC CHC acute abdomen differential diagnosis dyslipidemia hypertriglyceridemia treatment

Searching the Web

NHM India dyslipidemia hypertriglyceridemia standard treatment guidelines fibrate statin dose 2023 2024

You've run out of free credits. Sign up for a free account to continue using Orris.
This is a shared conversation. Sign in to Orris to start your own chat.