What is the treatment for a patient with deliberate self-harm involving yellow phosphorus rodenticide?

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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

References

Guideline

Management of Zinc Phosphide Ingestion

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Rodenticide Poisoning: Critical Appraisal of Patients at a Tertiary Care Center.

Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine, 2020

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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