Acute Quetiapine Overdose in Adults: A 5-Year Retrospective Case Series
Study objective
To describe clinical effects and outcome after acute quetiapine overdose in adults and compare these with overdose by all other antipsychotic drugs as a group.
Methods
We performed a 5-year (2002 to 2006) retrospective case series by chart review of the California Poison Control System database for adult patients with acute ingestion of quetiapine. Patients with coingestants were excluded. Symptoms, signs, and medical outcomes were extracted from the database and also by direct chart review for some variables (QRS- and QT-interval prolongation, torsades de pointes).
Results
We found 945 cases meeting criteria for analysis. Intentional ingestions accounted for 87% of cases. Patient ages ranged from 18 to 84 years, with a median of 35 years. There were 3 deaths, all of whom had coma, tachycardia, and respiratory depression requiring ventilatory support. Clinical manifestations included drowsiness (76%), coma (10%), seizures (2%), tachycardia (56%), hypotension (18%), and respiratory depression (5%). There were insufficient data to determine the incidence of QRS or QT prolongation in our study group, but only 2 patients were reported to have ventricular tachycardia and neither was described as having torsades de pointes. Compared with overdose by all other antipsychotic agents as a group, quetiapine was more likely to cause hypotension (odds ratio [OR] 2.05; 95% confidence interval [CI] 1.52 to 2.76), coma (OR 2.16; 95% CI 1.46 to 3.20), and respiratory depression (OR 2.49; 95% CI 1.40 to 4.41); require tracheal intubation (OR 1.92; 95% CI 1.41 to 2.61); and result in death or a major medical outcome (OR 2.62; 95% CI 1.78 to 3.85).
Conclusion
Consequences of acute quetiapine overdose included coma, respiratory depression, and hypotension, and these complications were more common compared with overdose by all other antipsychotic agents as a group.
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Supervising editor: E. Martin Caravati, MD, MPH
Author contributions: Each of the authors made substantial contributions to conception and design and analysis and interpretation of the data; had a role in drafting the article or revising it critically for important intellectual content; and approved of the version to be published. AN and KRO conceived of and designed the study and obtained consent from the University of California, San Francisco Committee on Human Research. AN, MC, and KRO were responsible for data collection, and KRO supervised conduct of the study. AN, MC, and KRO performed data analysis and interpretation. AN drafted the article, MC and KRO provided significant input, and KRO contributed substantially to its revision. All 3 authors approve of the final article. AN guarantees the scientific integrity of the study presented. AN takes responsibility for the paper as a whole.
Funding and support: By Annals policy, all authors are required to disclose any and all commercial, financial, and other relationships in any way related to the subject of this article that might create any potential conflict of interest. The authors have stated that no such relationships exist. See the Manuscript Submission Agreement in this issue for examples of specific conflicts covered by this statement.
Publication dates: Available online April 23, 2008.
Reprints not available from the authors.
PII: S0196-0644(08)00608-2
doi:10.1016/j.annemergmed.2008.03.016
© 2008 American College of Emergency Physicians. Published by Elsevier Inc. All rights reserved.
