Therapeutic Dosing of Pralidoxime Chloride

Author:

Thompson Dennis F.1,Thompson G. Dail2,Greenwood Robert B.3,Trammel Harold L.4

Affiliation:

1. Drug Information Service, State of Oklahoma Teaching Hospitals, and Clinical Associate Professor of Pharmacy, University of Oklahoma Health Sciences Center, Oklahoma City, OK;

2. Department of Pharmacy, Baptist Medical Center, Oklahoma City, OK;

3. Pharmacokinetics and Pharmaceutics, School of Pharmacy, Campbell University, Buics Creek, NC;

4. Center Operations, National Animal Poison Control Center, University of Illinois, Urbana, IL.

Abstract

Pralidoxime chloride is a useful agent in the treatment of organophosphate poisoning. Poisindex, a widely used poisoning treatment resource, recommends dosing pralidoxime chloride as an intermittent iv infusion every 8–12 hours, whereas other authors have used continuous iv infusion with good results. Available animal data suggest that a serum concentration of 4 μg/ml may be a minimal level to protect against the toxic effects of organophosphates. Pharmacokinetic simulations, based on parameters obtained from healthy nonpoisoned subjects, show that pralidoxime levels fall rapidly to <4 μg/ml within 1.5–2 hours after a 1-g iv bolus. Continuous iv infusion (0.5 g/h) maintains pralidoxime levels >4 μg/ml throughout the length of infusion. We conclude that continuous iv infusion of pralidoxime chloride may be the preferred method of administration in patients with acute organophosphate poisoning. Clinical trials will be necessary to document the effectiveness of this regimen.

Publisher

SAGE Publications

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

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