Effect of anticholinergic drugs on the efficacy of activated charcoal

Robert Green, Daniel S. Sitar, Milton Tenenbein

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)

Abstract

Background: Although it is a commonly held belief that the ingestion of drugs with an anticholinergic action would prolong the duration of time after drug ingestion for effective gastrointestinal decontamination, data are lacking to support this belief. The purpose of this study is to determine whether activated charcoal is more effective in the presence of concurrent anticholinergic activity. Methods: A three-limbed randomized crossover study in 10 healthy volunteers was completed to determine the ability of a 50 g dose of activated charcoal to reduce the bioavailability of a simulated overdose of acetaminophen (12 × 325 mg tablets) in the presence and absence of a concurrently present anticholinergic drug, atropine (0.01 mg/kg I. M. administered 15 min prior to the acetaminophen ingestion). Results: After the acetaminophen ingestion, median Cmax occurred at l h for all three exposures but was lower in the atropine-treated study arm (31±19 mg/L) than in the control or charcoal alone intervention arms (49±13 and 51±16 mg/L, respectively) (P<0.05). Compared to the control area under the serum concentration vs. time curve, a single dose of activated charcoal 1 h after drug ingestion reduced acetaminophen bioavailability by 20% (95% CI 4-36%) and by 47% (95% CI 35-59%) in the presence of atropine (P<0.05 atropine plus charcoal vs. charcoal alone). Conclusions: Our data support the belief that activated charcoal is more effective in the presence of anticholinergic activity. Additional study is required to determine whether in patients with anticholinergic drug overdose, activated charcoal is effective at times beyond the recommendation for overdoses of drugs without this pharmacodynamic effect.

Original languageEnglish
Pages (from-to)267-272
Number of pages6
JournalJournal of Toxicology - Clinical Toxicology
Volume42
Issue number3
DOIs
Publication statusPublished - 2004
Externally publishedYes

Bibliographical note

Funding Information:
This investigation was funded by a grant from the Children’s Hospital Foundation of Manitoba.

ASJC Scopus Subject Areas

  • Toxicology
  • Health, Toxicology and Mutagenesis

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