What is the recommended management, including lethal dose, for a patient who has ingested aluminium phosphide (Celphos)?

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Management of Aluminum Phosphide (Celphos) Poisoning

Aluminum phosphide poisoning is a medical emergency with mortality exceeding 70%, requiring immediate ICU-level care for all exposures, as ingestion of as little as 150-500 mg can be fatal. 1

Lethal Dose and Toxicity

  • The lethal dose is 150-500 mg of aluminum phosphide, which corresponds to approximately 1-3 tablets, as each tablet typically contains 56% aluminum phosphide (approximately 500-600 mg per 1g tablet). 1
  • Toxicity results from phosphine gas released when aluminum phosphide contacts moisture in the gastrointestinal tract, causing mitochondrial dysfunction, free radical generation, and multi-organ failure. 2
  • Mortality rates exceed 70% even with aggressive treatment, with circulatory failure and severe hypotension being the most common causes of death. 2

Immediate Safety Measures

Healthcare Worker Protection (CRITICAL FIRST STEP)

  • All healthcare personnel must wear full-face gas masks and butyl rubber gloves before any patient contact—ordinary surgical masks and latex gloves do not protect against phosphine vapor. 3
  • Never initiate patient care without proper personal protective equipment, as secondary phosphine exposure has caused severe illness requiring ICU admission, atropine, pralidoxime, and prolonged intubation in healthcare workers. 3, 1
  • Remove contaminated clothing immediately outside the hospital to prevent vapor generation inside the facility. 3
  • Ensure treatment areas are well-ventilated, as poorly ventilated spaces have resulted in healthcare worker poisoning requiring intensive interventions. 3, 1

Gastrointestinal Decontamination

  • Perform extensive gastric lavage with a mixture of coconut oil and sodium bicarbonate solution as soon as possible after presentation. 4, 5
  • Coconut oil may prevent further absorption of aluminum phosphide and has shown positive clinical significance in case reports of survival after lethal dose ingestion. 4
  • Activated charcoal can be considered for gastrointestinal decontamination, although its ability to adsorb phosphine gas is uncertain. 1
  • Administer oral sodium bicarbonate and sorbitol suspension following gastric lavage. 4

Cardiovascular Support

  • Initiate aggressive fluid resuscitation and vasopressor support immediately for the near-universal hypotension and circulatory failure. 6, 1
  • Noradrenaline and dopamine infusions should be started for hypotension and titrated to maintain adequate perfusion. 7
  • Administer calcium gluconate (100-200 mg/kg/dose) via slow IV infusion with continuous ECG monitoring for life-threatening arrhythmias and cardiac membrane stabilization. 1
  • Do not administer sodium bicarbonate and calcium through the same IV line to avoid precipitation. 1
  • Continuous cardiac monitoring is mandatory, as cardiotoxicity including atrial fibrillation, ST elevation, and myocardial infarction can develop hours after ingestion. 8

Respiratory Management

  • Administer 100% oxygen immediately via high-flow mask or endotracheal tube to all suspected cases while awaiting confirmation. 3
  • Continue high-flow oxygen until metabolic acidosis resolves and respiratory symptoms improve. 3
  • Intubate patients with respiratory distress or loss of consciousness using low tidal-volume ventilation (≤6 mL/kg ideal body weight) with moderate PEEP. 3
  • Target normoventilation with arterial PaCO₂ of 5.0-5.5 kPa—avoid hyperventilation because it worsens tissue perfusion and increases mortality. 3
  • CPAP may be considered only for conscious, cooperative patients without contraindications such as full stomach or bowel paralysis. 3, 1

Metabolic Acidosis Management

  • Administer sodium bicarbonate (1-2 mEq/kg IV push) for severe metabolic acidosis, which is a near-universal finding in aluminum phosphide poisoning. 1, 4, 7
  • Continue IV sodium bicarbonate infusion as needed to maintain pH >7.2, guided by serial arterial blood gas measurements. 4, 7

Magnesium Sulfate Administration

  • Administer intravenous magnesium sulfate to reduce cardiac arrhythmias and mortality, though there is no uniformity in dosing worldwide. 8, 4
  • Magnesium sulfate has well-documented benefit in reducing arrhythmias associated with aluminum phosphide poisoning. 8

Renal Replacement Therapy

  • Consider hemodialysis for severe poisoning, particularly when metabolic acidosis is refractory to bicarbonate therapy or multi-organ failure develops. 7
  • Hemodialysis contributed to symptomatic treatment and survival in documented cases of cardiac arrest from aluminum phosphide poisoning. 7
  • High-flux dialysis membranes are preferred if aluminum toxicity is suspected. 1

Management of Aluminum Toxicity (If Suspected)

  • Measure serum aluminum levels if aluminum toxicity is suspected, particularly in patients requiring prolonged intensive care. 1
  • For serum aluminum levels between 60-200 µg/L, administer deferoxamine (DFO) at 5 mg/kg intravenously with careful monitoring, using high-flux dialysis membranes to enhance clearance of aluminum-DFO complexes. 1
  • For serum aluminum levels >200 µg/L, deferoxamine must be withheld due to high risk of precipitating acute aluminum neurotoxicity; instead, initiate intensive high-flux hemodialysis daily for 4-6 weeks until levels decline. 9, 1
  • Fatal mucormycosis can occur with DFO therapy, with 91% mortality in dialysis patients, so reduced dosing and expanded intervals minimize this risk. 1

Monitoring and Complications

  • Observe for delayed neuromuscular weakness that may appear up to four days after exposure, potentially necessitating prolonged ventilatory support. 3
  • Screen for rhabdomyolysis by tracking creatine kinase and potassium levels, as calcium-mediated myonecrosis can lead to respiratory muscle weakness. 3, 1
  • Monitor for multi-organ failure including hepatic injury, acute renal failure, and acute respiratory distress syndrome. 2, 4
  • Serial ECGs and cardiac troponin levels should be obtained to detect evolving cardiotoxicity. 8

Critical Pitfalls to Avoid

  • Hyperventilation strategies must be avoided because they exacerbate tissue hypoxia and increase mortality. 3
  • Avoid physical restraints without adequate sedation, as this can worsen outcomes. 1
  • Avoid succinylcholine or mivacurium for intubation if cholinesterase inhibition is suspected. 1
  • Do not use aluminum hydroxide as a phosphate binder for more than 1-2 days to avoid cumulative aluminum toxicity. 1
  • Hyperbaric oxygen therapy has no role in aluminum phosphide poisoning and is contraindicated due to hemodynamic instability and the need for continuous bedside intensive care. 6

Prognosis

  • Despite aggressive supportive care, mortality remains extremely high at 70% or greater. 2
  • Survival rates of 42% have been reported with the comprehensive treatment regimen including coconut oil gastric lavage, aggressive cardiovascular support, and hemodialysis. 5
  • Early presentation and rapid initiation of treatment improve survival, though even patients presenting within 6 hours can develop fatal complications. 8, 4

References

Guideline

Management of Aluminum Phosphide Poisoning in ICU

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Aluminum phosphide poisoning: an unsolved riddle.

Journal of applied toxicology : JAT, 2011

Guideline

Airway Protection and Respiratory Management in Aluminum Phosphide Poisoning

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Contraindications of Hyperbaric Oxygen Therapy in Aluminum Phosphide Poisoning

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Successful Management of Aluminium Phosphide Poisoning Resulting in Cardiac Arrest.

Turkish journal of anaesthesiology and reanimation, 2015

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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