What is the management for Datura poisoning?

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Management of Datura Poisoning

The management of Datura poisoning requires immediate supportive care, activated charcoal for decontamination, and physostigmine (0.02 mg/kg IV/IM) as a specific antidote for severe anticholinergic toxicity. 1, 2

Clinical Presentation

Datura poisoning presents with an anticholinergic toxidrome characterized by:

  • Central nervous system effects: confusion, delirium, hallucinations, agitation, coma
  • Peripheral effects: mydriasis, tachycardia, hyperthermia, dry mouth, dry skin, urinary retention
  • "Hot as a hare, blind as a bat, dry as a bone, red as a beet, mad as a hatter" 3, 4, 5

Management Algorithm

1. Initial Stabilization

  • Secure airway: Early endotracheal intubation for severe poisoning or altered mental status
  • Support breathing: Provide mechanical ventilation as needed
  • Maintain circulation: IV fluids for hypotension, position unconscious patients in left lateral head-down position
  • Continuous cardiac monitoring 1

2. Decontamination

  • Administer activated charcoal in repeated doses (within 1-2 hours of ingestion)
  • Do not induce vomiting or administer anything by mouth unless advised by poison control 1, 3

3. Specific Antidote

  • Physostigmine for severe anticholinergic toxicity:
    • Adult dose: 0.5-2 mg IV slowly (no more than 0.5 mg per minute)
    • Pediatric dose: 0.02 mg/kg IM or slow IV
    • May repeat at 5-10 minute intervals if toxic effects persist and no cholinergic effects appear
    • Maximum total dose: 2 mg 2, 4

4. Supportive Care

  • Cooling measures for hyperthermia (external and internal cooling)
  • IV fluids for hydration and to maintain blood pressure
  • Benzodiazepines for agitation and seizures
  • Monitor for and treat rhabdomyolysis to prevent renal failure
  • Bladder catheterization for urinary retention 1, 3

Evidence for Physostigmine Use

Physostigmine is particularly effective for Datura poisoning because:

  • It crosses the blood-brain barrier and reverses both central and peripheral anticholinergic effects
  • Studies show earlier resolution of central nervous system toxicity in patients who received physostigmine compared to those who did not 4
  • No adverse events were reported from physostigmine administration in a study of Datura poisoning cases 4

Contraindications to Physostigmine

Exercise caution with physostigmine in patients with:

  • Cardiovascular disease
  • Asthma
  • Mechanical obstruction of intestine or urinary tract
  • Concurrent use of cholinesterase inhibitors 2

Duration of Monitoring

  • Patients should be monitored for at least 24-36 hours after ingestion
  • Anticholinergic effects may persist for days, particularly visual accommodation difficulties 3, 6
  • Continuous cardiac monitoring is essential due to risk of dysrhythmias 1

Additional Considerations

  • Contact regional poison centers for expert guidance (US: 1-800-222-1222) 7, 1
  • Datura poisoning can be accidental (medicinal use, misidentification) or intentional (recreational use, criminal poisoning) 4, 8
  • Parts of the plant other than flowers are associated with more severe poisoning 4

Pitfalls to Avoid

  • Delaying antidote administration while waiting for confirmatory testing
  • Failing to recognize the anticholinergic toxidrome
  • Discharging patients too early (symptoms can persist or recur)
  • Overlooking the possibility of co-ingestants or adulterants 1

References

Guideline

Management of Poisoning

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Acute poisoning due to ingestion of Datura stramonium - a case report.

Romanian journal of anaesthesia and intensive care, 2017

Research

Datura fruit poisoning.

The Medical journal of Malaysia, 2018

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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