Immediate Management of Organophosphate Poisoning
Administer atropine 1–2 mg IV immediately for adults (0.02 mg/kg for children, minimum 0.1 mg), doubling the dose every 5 minutes until full atropinization is achieved, while simultaneously giving pralidoxime 1–2 g IV loading dose followed by continuous infusion, along with benzodiazepines for seizures and early intubation for life-threatening cases. 1, 2, 3, 4
Personal Protection and Decontamination (First Priority)
- Use full personal protective equipment (PPE) before approaching the patient – organophosphates are readily absorbed through skin and respiratory tract, and healthcare workers have required atropine, pralidoxime, and intubation after secondary exposure from handling contaminated clothing or gastric contents. 5, 1
- Remove all contaminated clothing immediately and irrigate skin copiously with soap and water – this stops ongoing absorption and prevents secondary exposure to staff. 1, 2
- Never handle gastric contents, vomit, or contaminated materials without PPE – documented cases show severe poisoning in healthcare workers from this route. 1
Atropine: The Immediate Life-Saving Intervention (Class 1, Level A Evidence)
Initial Dosing Algorithm
- Adults: 1–2 mg IV bolus immediately upon recognition of severe poisoning (bronchospasm, bronchorrhea, bradycardia, seizures). 1, 2, 3
- Children: 0.02 mg/kg IV (minimum 0.1 mg, maximum single dose 0.5 mg per dose). 1, 3
- This initial dose is substantially higher than the 0.5–1.0 mg used for bradycardia from other causes – organophosphate poisoning demands aggressive treatment from the outset. 3
Dose Escalation Protocol (Critical)
- Double the atropine dose every 5 minutes until all atropinization endpoints are met – this is not a fixed-dose repetition schedule but an aggressive escalation strategy. 1, 2, 3
- Continue escalation regardless of heart rate – tachycardia is an expected pharmacologic effect and is NOT a contraindication to continued dosing. 1, 2
- The tachycardia may originate from nicotinic receptor overstimulation by the organophosphate itself, not from atropine. 1, 2
Endpoints of Atropinization (All Must Be Achieved)
- Clear chest on auscultation (resolution of bronchorrhea) 2, 3
- Heart rate >80 beats/min 2, 3
- Systolic blood pressure >80 mm Hg 2, 3
- Dry skin and mucous membranes 2, 3
- Mydriasis (pupil dilation) 2, 3
Expected Atropine Requirements
- Typical cumulative doses: 10–20 mg in the first 2–3 hours. 1, 3
- Severe cases may require up to 50 mg in the first 24 hours – one case report documented nearly 1000 mg total over the course of treatment. 3, 6
- The therapeutic endpoint is control of muscarinic symptoms, not heart rate normalization – undertreating organophosphate poisoning is far more dangerous than atropine-induced tachycardia. 1, 2
Maintenance Atropine Infusion
- After achieving initial atropinization, administer 10–20% of the total loading dose per hour (up to 2 mg/h in adults) as a continuous infusion. 1, 3
- Continuous infusion is preferred over intermittent boluses for maintenance. 3
- Maintain atropinization for at least 48–72 hours – delayed complications and relapses can occur, especially with ingested organophosphates due to continued GI absorption. 2, 4
Pralidoxime (Oxime Therapy): Essential Concurrent Treatment (Class 2a, Level A Evidence)
Mechanism and Timing
- Pralidoxime reactivates acetylcholinesterase by competing with the organophosphate-enzyme bond – it reverses nicotinic effects (muscle weakness, respiratory paralysis) that atropine cannot address. 1, 2
- Administer early, ideally within minutes to hours after exposure – the organophosphate-enzyme complex undergoes "aging" (becomes irreversible), with timing varying by agent: soman ages within minutes, while agricultural organophosphates may allow a 24-hour window, though efficacy drops 50% after 6 hours. 1
- Do not withhold pralidoxime when the class of poison (organophosphate vs. carbamate) is unknown. 1
Dosing Protocol
- Adults: 1–2 g IV loading dose administered slowly over 15–30 minutes, preferably as an infusion in 100 mL normal saline. 1, 4
- If pulmonary edema is present or infusion is not practical, give slowly over at least 5 minutes as a 50 mg/mL solution. 4
- Children: 25–50 mg/kg IV loading dose over 15–30 minutes. 1
Maintenance Infusion
- Adults: 400–600 mg/hour continuous infusion. 1, 4
- Children: 10–20 mg/kg/hour continuous infusion. 1
- Evidence suggests continuous infusion maintains therapeutic levels longer than intermittent boluses. 4
- A second loading dose of 1000–2000 mg may be indicated after 1 hour if muscle weakness persists. 4
- Additional doses may be given every 10–12 hours if muscle weakness continues. 4
Critical Safety Considerations
- Infuse pralidoxime slowly – rapid infusion can cause temporary worsening of cholinergic manifestations (tachycardia, cardiac arrest, laryngospasm, muscle rigidity), with intermittent infusion rate not exceeding 200 mg/minute. 4
- Common adverse effects include transient hypotension, reduced cardiac output, dizziness, blurred vision, nausea, and muscle rigidity. 1
- Atropine must always be administered concurrently – pralidoxime alone is insufficient to manage respiratory depression. 1, 2
Airway Management and Ventilatory Support
- Perform early endotracheal intubation for life-threatening organophosphate poisoning – observational data suggest better outcomes with early intubation in significant poisoning. 1, 2
- Avoid succinylcholine and mivacurium for intubation – these neuromuscular blockers are metabolized by cholinesterase and are absolutely contraindicated in organophosphate poisoning. 1, 2, 4
- Use alternative neuromuscular blockers (rocuronium, vecuronium) if paralysis is needed. 1
Seizure and Agitation Management
- Administer benzodiazepines immediately for seizures or agitation. 1, 2
- Diazepam: 0.2 mg/kg IV in fractionated doses (first-line). 1, 2
- Midazolam: 0.05–0.1 mg/kg IV as alternative. 1, 2
- Benzodiazepines also facilitate mechanical ventilation when needed. 1
Monitoring and Observation Period
- Maintain close observation for at least 48–72 hours – fatal relapses have been reported after initial improvement, particularly with ingested organophosphates due to continued absorption from the lower bowel. 2, 4
- Continuous cardiac monitoring to detect dysrhythmias – but do not use heart rate to limit atropine dosing. 2
- Serial respiratory assessments every 5–10 minutes during the escalation phase. 2
- Monitor for delayed complications: intermediate syndrome (muscle weakness 24–96 hours post-exposure), rhabdomyolysis, myonecrosis, and renal damage. 1, 7
Special Complications and Pitfalls
Atropine-Related Concerns
- Fever from repeated atropine is an expected adverse effect – never withhold or prematurely discontinue atropine due to fever, as inadequate atropinization leads to respiratory failure and death. 1
- Fever may have multiple etiologies: atropine's central effects, nicotinic-induced muscle fasciculations, or aspiration pneumonia from bronchorrhea. 1
Rhabdomyolysis and Myonecrosis
- Severe myonecrosis can occur from excessive acetylcholine causing calcium flux into skeletal muscle, leading to myocyte death. 1
- Monitor creatine kinase and potassium levels for rhabdomyolysis detection. 1
- Reddish urine indicates myoglobin (muscle breakdown), not hemoglobin – treat with adequate hydration, forced diuresis, and urine alkalinization. 1
Gastric Decontamination Hazards
- If nasogastric lavage is performed, ensure all staff wear full PPE – gastric contents contain organophosphates that can cause severe secondary poisoning in healthcare workers. 1
Drugs to Avoid
- Do not use morphine, theophylline, aminophylline, reserpine, or phenothiazine-type tranquilizers – these are contraindicated in organophosphate poisoning. 4
- Use succinylcholine with extreme caution or avoid entirely – prolonged paralysis has been reported when given with anticholinesterase activity. 4
Summary Algorithm
- PPE and decontamination (remove clothing, wash skin) 1
- Atropine 1–2 mg IV immediately, double every 5 minutes until full atropinization 1, 2, 3
- Pralidoxime 1–2 g IV loading dose, then 400–600 mg/hour infusion 1, 4
- Benzodiazepines for seizures/agitation 1, 2
- Early intubation if life-threatening (avoid succinylcholine/mivacurium) 1, 2
- Continuous monitoring for 48–72 hours minimum 2, 4