Management of Organophosphate Poisoning
The management of organophosphate (OP) poisoning requires immediate administration of atropine and pralidoxime, along with supportive care, decontamination, and close monitoring for respiratory failure, which is the most common cause of mortality. 1
Initial Assessment and Diagnosis
Diagnosis is primarily based on:
- History of exposure
- Clinical presentation (SLUDGE syndrome: Salivation, Lacrimation, Urination, Defecation, GI upset, Emesis)
- Measurement of cholinesterase activity in blood (reduction below 50% of normal indicates poisoning)
Key clinical features to recognize:
- Muscarinic effects: miosis, bronchorrhea, bronchospasm, bradycardia, hypersalivation
- Nicotinic effects: muscle fasciculations, weakness, paralysis
- Central effects: altered mental status, seizures, confusion 1
Treatment Algorithm
1. Immediate Interventions
- Ensure healthcare provider safety with appropriate PPE before approaching patient
- Remove patient from exposure source
- Perform decontamination (remove contaminated clothing, wash skin/hair with soap and water) before patient enters healthcare facility 1
2. Antidote Administration
Atropine:
Pralidoxime (PROTOPAM):
3. Respiratory Management
- Early recognition of respiratory failure is crucial
- Indications for intubation and mechanical ventilation:
- Respiratory failure
- Depressed level of consciousness with inability to protect airway
- Hemodynamic instability
- Ventilation strategy: synchronized intermittent mandatory ventilation + pressure support mode 1, 3
4. Supportive Care
- Monitor cholinesterase activity, creatine kinase, and serum potassium levels
- Continue treatment until depressed cholinesterase activity is reversed
- Maintain observation for at least 48-72 hours due to risk of delayed absorption and relapse 1, 2
Special Considerations
Contraindications
- Avoid the following medications in OP poisoning:
Complications to Monitor
- Intermediate syndrome (19.1% of cases)
- Respiratory failure (74.4% of cases)
- Aspiration pneumonia
- Neurologic impairment
- Acute respiratory distress syndrome (ARDS) 1, 3
Prognostic Factors
Poor prognostic indicators include:
- Low Glasgow Coma Scale on admission
- High APACHE II and SOFA scores
- Delayed time to treatment initiation
- Elevated serum LDH levels 4
- Need for mechanical ventilation (50% mortality vs 21.6% in non-ventilated patients) 3
Pitfalls and Caveats
Delayed recognition: Symptoms may be mistaken for other conditions. Always consider OP poisoning in patients with cholinergic symptoms, especially with history of exposure.
Inadequate decontamination: Secondary contamination of healthcare providers is a serious risk. Ensure proper decontamination before the patient enters the healthcare facility.
Insufficient atropinization: Underdosing atropine is common. Continue dosing until secretions are controlled.
Delayed pralidoxime administration: Efficacy decreases with time. Administer as soon as possible, ideally within 36 hours of exposure.
Missing continued absorption: Fatal relapses can occur due to continued absorption from the lower bowel. Continue monitoring and "titrate" with pralidoxime as needed for recurring signs of poisoning. 1, 2
Respiratory failure recognition: Watch for increasing respiratory rate (from 22 to 38 breaths/min) as an early sign of respiratory distress requiring immediate intervention. 3