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Organophosphate and Carbamate Poisoning

 

Epidemiology: 200K fatalities worldwide every year

 

DDx: Cholinesterase inhibitors, Cholinomimetics, Nicotine alkaloids

 

Kinetics: Absorption via ingestion, inhalation or topical contact. Minutes to hours depending on lipophilicity, metabolism and toxicity of compound

 

Pathophysiology: Inhibition of AChE by phosphorylating active site > Cholinergic crisis > If inhibition is prolonged AChE can be irreversibly inhibited (“aging” which does not occur with carbamates)

 

Clinical features: Miosis most commonly encountered symptom. Fatality usually due to respiratory failure.

 

Cholinergic effects at post ganglionic muscarinic fibers:

SLUDGE/BBB – Salivation, Lacrimation, Urination, Defecation, Gastric Emesis, Bronchorrhea, Bronchospasm, Bradycardia

DUMBELS – Defecation, Urination, Miosis, Bronchorrhea/Bronchospasm/Bradycardia, Emesis, Lacrimation, Salivation

 

Cholinergic effects at postganglionic sympathetic fibers: tachycardia. mydriasis, bronchodilation, leukocytosis, urinary retention, hyper or hypotension, hyper or hypoglycemia, and ketosis

 

Nicotinic effects at NMJ and postganglionic sympathetic fibers: fasciculations, muscle weakness, paralysis

 

Delayed Syndromes: Intermediate Neurologic Syndrome, Organophosphorus agent induced delayed neuropathy

 

Diagnosis: Largely clinical, Atropine challenge 1mg of Atropine in adults, 0.1-0.2mg atropine in children, serum or rbc cholinesterase levels

 

Management: IV, O2, Monitor

 

Atropine: Competitive muscarinic receptor antagonist. Treats muscarinic symptoms, most importantly bronchorrhea and bronchospasm

Adults 2-5mg doubling dose q 3-5 minutes until atropinization occurs

Children 0.05-0.1 mg/Kg dose q 3-5 minutes until atropinization occurs

After atropinization give 10-20% total loading dose per hour. If anticholinergic symptoms occur, pt likely has atropine toxicity

 

Pralidoxime (2-Pam): Reactivates AChE. Treats both muscarinic and nicotinic symptoms

Adults 30mg/kg bolus followed by 8mg/kg/hr infusion

Children 20-50mg/kg bolus followed by 10-20mg/kg/hr infusion

 

Intubation: Avoid Succinlycholine, Use non-depolarizing agents

Seizures: Benzodiazepines

Decontamination: Remove and discard clothes. Consider activated charcoal if within one hour of ingestion

Poison control

 

Prognosis: GCS less than 13, lipophilic OPs such as fenthion and parathion, all associated with poor prognosis

 

Disposition: ICU.

 

References

  • Eddleston, M., Buckley, N. A., Eyer, P., & Dawson, A. H. (2008). Management of acute organophosphorus pesticide poisoning. The Lancet, 371(9612), 597-607.
  • RF Clark (2002),Insecticides: organic phosphorus compounds and carbamates
  • Goldfrank’s Toxicological Emergencies (7th edn.), McGraw-Hill Professional, New York pp. 1346–1360
  • Sungur, M., & Güven, M. (2001). Intensive care management of organophosphate insecticide poisoning. Critical care, 5(4), 211.
  • Worek, F., Koller, M., Thiermann, H., & Szinicz, L. (2005). Diagnostic aspects of organophosphate poisoning. Toxicology, 214(3), 182-189.
  • Lee, P., & Tai, D. Y. H. (2001). Clinical features of patients with acute organophosphate poisoning requiring intensive care. Intensive care medicine, 27(4), 694-699.
  • Rusyniak, D. E., & Nanagas, K. A. (2004, June). Organophosphate poisoning. In Seminars in neurology (Vol. 24, No. 2, pp. 197-204).

 

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Jay Khadpe MD

  • Editor in Chief of "The Original Kings of County"
  • Assistant Professor of Emergency Medicine
  • Assistant Residency Director
  • SUNY Downstate / Kings County Hospital

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Categories: Morning Report

Jay Khadpe MD

  • Editor in Chief of “The Original Kings of County”
  • Assistant Professor of Emergency Medicine
  • Assistant Residency Director
  • SUNY Downstate / Kings County Hospital

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