Objective: The recent American Academy of Clinical Toxicology/European Asso
ciation of Poisons Centres and Clinical Toxicologists position statement on
activated charcoal stated "there are insufficient data to support or exclu
de its use after 1 hour of ingestion." The purpose of this study was to det
ermine the effectiveness of activated charcoal administered 1, 2, and 3 hou
rs after drug ingestion. Methods: This was a human volunteer, randomized cr
ossover study. Ten volunteers ingested 4 g of acetaminophen on jour occasio
ns at least 1 week apart. One ingestion sen,ed as a control and the other t
hree as experimental ingestions with charcoal being administered at 1, 2, a
nd 3 hours after acetaminophen dosing. Eight blood specimens were obtained
over the initial 8 hours for serum acetaminophen concentrations that were u
sed for calculation of routine pharmacokinetic parameters. Repeated measure
s of ANOVA and Tukey's HSD test were used for statistical analysis. Results
: Pharmacokinetic parameters for acetaminophen in our volunteers were consi
stent with literature values. The mean area under the curve (AUC +/- SD) fo
r the control and the 1-, 2-, and 3-hour groups were 221 +/- 54, 154 +/- 71
, 206 +/- 67 and 204 +/- 58 mg/L/h, respectively. The 1-hour group was the
only one differing from control (p < 0.01). The decrease of bioavailability
at 1 hour was 30.3%, which is similar to previous studies. Conclusion: Our
data do not support the administration of activated charcoal as a gastroin
testinal decontamination strategy beyond 1 hour after drug overdose.