Snake Bite 🔥🔥🔥

Epidemiology and Pathophysiology

• Snakebite is a neglected tropical disease with the highest burden existing in South Asia, South East Asia, and sub-Saharan Africa.
• In India, approximately $45,900$ deaths are attributed to snake bites annually, with more than $25\mathrm{\%}$ of these deaths occurring in children aged $5-14$ years.
• The "Big Four" most important venomous snakes in India are the Indian cobra (Naja naja), Indian krait (Bungarus caeruleus), Russell's viper (Daboia russelii), and saw-scaled viper (Echis carinatus).
• Snake venom is a highly complex mixture containing more than $100$ toxic and non-toxic proteins, peptides, carbohydrates, lipids, and amines.
• The average dry weight of venom injected at a strike is approximately $60$ mg in N. naja, $13$ mg in E. carinatus, and $63$ mg in D. russelii.
• The exact same amount of venom affects children much more severely than adults because the total serum volume of distribution is significantly smaller in children.

Clinical Manifestations

• The diagnosis of snake envenomation is primarily clinical, based on a history of snake bite, presence of fang marks, local manifestations (pain and swelling), and systemic signs of neurotoxicity or bleeding.
• Specific systemic manifestations correlate strongly with the species of the offending snake.
• Clues suggesting severe envenomation include rapid early extension of local swelling, early tender enlargement of local lymph nodes, early systemic collapse (shock, severe headache, pathological drowsiness, early ptosis), early spontaneous bleeding, and the passage of dark brown or black urine.

Diagnostic and Laboratory Evaluation

• The $20$-minute Whole Blood Clotting Time ($20$-min WBCT) is the primary bedside diagnostic test used to confirm hemotoxic (Viperine) envenomation.
• To perform the $20$-min WBCT: leave a few milliliters of venous blood undisturbed for exactly $20$ minutes in a clean, new, and dry test tube; then tip the tube. The absence of clotting confirms a hemotoxic bite.
• While the $20$-min WBCT is useful, emergency treatment with snake antivenom (SAV) must be based on overall clinical assessment as the test takes time to perform.
• Ancillary laboratory studies should include hemoglobin/hematocrit, platelet count, white blood cell count, peripheral blood film, muscle and liver enzymes, and electrolytes.
• Arterial blood gases should be performed if indicated, but arterial punctures are strictly contraindicated in patients with active bleeding or coagulopathy.

Emergency Management

Pre-Hospital and First Aid

• First aid measures must focus on immediate immobilization and rapid transport, completely avoiding harmful traditional practices.
• Walking for $>10$ minutes after a bite is a significant risk factor for severe systemic venom absorption; the patient must be carried or transported via vehicle/stretcher.

Initial Assessment and Supportive Care

• An ABCDE approach should be immediately utilized in all children presenting with a history of snake bite, assessing for airway patency, breathing patterns, and maintaining normovolemia.
• Pain is common with snake bites; analgesics and narcotics (if no respiratory or CNS depression is present) are indicated, while local anesthetics can also be used.
• Prophylactic antibiotics are not indicated in snake bites unless the bite site has been actively manipulated with unhygienic local practices.
• Steroids and antihistamines have no proven role in prophylaxis against SAV reactions and should only be used to treat acute reactions, or in cases of refractory shock with adrenal insufficiency (Russell's viper).
• Supportive interventions encompass mechanical ventilation, inotropes, dialysis, blood product administration, and surgical debridement of necrotic tissue as needed.

Snake Antivenom (SAV) Administration

• SAV is specifically recommended for patients exhibiting systemic symptoms and/or extensive local involvement.
• Extensive local involvement is defined as severe swelling that crosses a joint, swelling that involves more than half the bitten limb within $48$ hours, swelling that continues $1$ hour after tourniquet removal, or the development of tender, enlarged lymph nodes in the drainage area.
• In India, polyvalent SAV raised in horses is used, which covers the four most important venomous snakes.
• The initial dose of SAV is $8-10$ vials, administered irrespective of the child's age or weight.
• The dose remains identical for children and adults because the snake injects the exact same amount of venom regardless of the victim's size.
• SAV should be administered under strict supervision either via the push technique ($1$ mL/minute) or as an intravenous infusion (diluted in $5-10$ mL/kg of isotonic fluid and infused over $1$ hour).
• Further doses of SAV are guided by sequential estimation: repeat the dose if there is persistence of blood incoagulability after $6$ hours, ongoing bleeding after $1-2$ hours, progression of weakness after $1-2$ hours, or persisting cardiovascular signs.
• For neuroparalytic bites, a diagnostic and therapeutic trial of neostigmine ($0.04$ mg/kg IM) along with atropine (to block muscarinic side effects) should be attempted in all cases.

Management of SAV Adverse Reactions

• Adverse reactions to SAV include early anaphylactoid reactions ($10-180$ minutes), pyrogenic reactions ($1-2$ hours), and delayed serum sickness ($1-12$ days).
• At the earliest sign of an anaphylactoid or pyrogenic reaction, SAV administration must be temporarily suspended immediately.
• Intramuscular epinephrine ($0.01$ mg/kg of $1:10,000$ solution) is the first-line and most effective treatment for early reactions.
• Following epinephrine, intravenous chlorpheniramine maleate ($0.2$ mg/kg) and intravenous hydrocortisone ($2$ mg/kg) should be administered.
• Once the patient is clinically stable and has recovered from the reaction, the SAV infusion should be cautiously restarted at a slower rate with continuous bedside monitoring.

Prognosis and Complications

• The overall mortality rate for severe snake envenomation ranges from $5\mathrm{\%}$ to $15\mathrm{\%}$.
• In survivors, the primary cause of long-term permanent disability is severe local tissue necrosis, which frequently requires extensive surgical debridement, skin grafting, and occasionally amputation of deep tissues.
• Cerebral hypoxia from delayed resuscitation or stroke can result in permanent neurological deficits.
• Poor prognostic factors heavily associated with mortality or severe morbidity in children include young age, early vomiting, profound neurotoxicity, elevated serum creatinine, severe thrombocytopenia, evident ecchymosis at admission, lack of immobilization, and any delay in the administration of SAV.