Treatment of Yellow Phosphorus Rodenticide Poisoning in Deliberate Self-Harm
Immediately activate emergency medical services and contact Poison Control Center without delay, as yellow phosphorus poisoning causes fulminant hepatic failure with 77.78% of deaths occurring from this complication within 2-8 days of exposure. 1, 2
Immediate Emergency Actions
Do not administer anything by mouth, induce vomiting, or perform gastric lavage unless specifically directed by Poison Control. 1 These interventions are contraindicated because:
- Vomiting increases risk of aspiration of toxic phosphine gas released from yellow phosphorus 1
- No human studies demonstrate clinical benefit from water or milk dilution 1
- Ipecac provides no benefit and causes harm 1
Activated charcoal (1 g/kg) via small-bore nasogastric tube may be administered only if recommended by Poison Control, though evidence for efficacy is limited. 1 The critical window is within 2 hours of exposure—survival rates are 97.87% with gastric decontamination within 2 hours versus 84.62% without (p=0.033). 2
Clinical Presentation Timeline
Expect a characteristic biphasic pattern with a deceptive symptom-free interval:
- First 24 hours: Conspicuous absence of signs and symptoms in most patients, with only initial nausea, vomiting, and diarrhea 3, 2
- 24-72 hours: Symptom-free "latent period" where patients appear stable with normal vitals 3, 2
- After 24-36 hours (range 18-72 hours): 72.73% of patients develop toxidrome with dominant manifestations 2
Never discharge patients during the latent period—this is when they appear deceptively well before catastrophic deterioration. 3
Specific Clinical Manifestations to Monitor
The dominant clinical features in order of frequency are:
- Abdominal pain (52.53%) 2
- Jaundice (22.21%) 2
- Coagulopathy (15.15%) 2
- Multi-organ failure (17.17%) 2
- Hepatic encephalopathy (10.10%) 2
- Refractory shock (10.10%) 2
- Acute kidney injury (7.08%) 2
Laboratory abnormalities include:
- AST/ALT elevation (48-50% of patients) 2
- Bilirubin elevation (22.21%) 2
- PT/INR prolongation (15.15%) 2
- Metabolic acidosis (10.12%) 2
- Serum creatinine elevation (7.08%) 2
Mortality Predictors Requiring Immediate Escalation
The following predict poor outcome and mandate urgent liver transplant evaluation:
- Delayed resuscitation beyond 2 hours 2
- Jaundice development 2, 4
- Hepatic encephalopathy 2, 4
- AST/ALT elevation >1000 IU/L 2
- Metabolic acidosis 2
- Refractory shock 2
- Coagulopathy with features of acute liver failure 4
Mortality is 9.1% overall, with 77.78% of deaths from fulminant hepatic failure occurring at mean 4.22 days post-exposure (range 2-8 days). 2
Supportive Management Strategy
No specific antidote exists—management is entirely supportive with bridge to liver transplantation for acute liver failure. 5, 4
Supportive measures include:
- Continuous renal replacement therapy (CRRT) as bridge to transplant 5
- Plasmapheresis with limited success in non-transplant candidates 5
- Cytosorb therapy in selected patients 5
- Meticulous monitoring for multi-organ dysfunction 4
Liver Transplantation Criteria
Liver transplantation is the definitive treatment for acute liver failure from yellow phosphorus poisoning, with good outcomes in both adults and children when performed without contraindications. 5
Early listing criteria should include:
- Development of hepatic encephalopathy 5, 3
- Coagulopathy unresponsive to vitamin K 5
- Lactic acidosis 5
- Multi-organ dysfunction syndrome 3
Success rates are very promising provided no transplant contraindications exist. 5 Separate expedited criteria for listing are important to ensure rapid evaluation of critical patients. 5
Psychiatric Assessment Requirements
A comprehensive mental health assessment must be undertaken after medical stabilization, as this represents deliberate self-harm. 6
The assessment should include:
- Formulation of factors contributing to self-harm 6
- Risk management plan development 6
- Evaluation by mental health professional 6
- Safety planning interventions 6
- Assessment of suicidal ideation and intent 6
Establish empathic therapeutic relationship during initial assessment, as negative clinical experiences perpetuate cycles of self-harm. 6
Critical Pitfalls to Avoid
Do not:
- Discharge during the 24-72 hour latent period when patients appear well 3, 2
- Delay EMS activation while attempting home interventions 1
- Administer oral fluids or induce vomiting 1
- Underestimate toxicity based on initial benign presentation 2, 4
- Delay transplant evaluation once hepatic encephalopathy develops 5
The deceptive symptom-free interval is the most dangerous period—patients who take discharge against medical advice during this window frequently return in fulminant hepatic failure. 3