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Abstract

Objective

Antipsychotic drug therapy is the cornerstone of treatment of persons with schizophrenia. Because most antipsychotics are metabolized by the hepatic cytochrome P450 system, concomitant use of an antipsychotic and medications that are competitively metabolized by the same system may cause a potentially harmful drug-drug interaction. This study used a large state's Medicaid claims database to examine the proportion of patients exposed to such interactions and the risk factors associated with exposure.

Methods

Claims from January 2000 through December 2003 for adult patients with a diagnosis of schizophrenia and at least one prescription for an antipsychotic (N=27,909) were examined for pairs of medications identified as potentially causing moderate or severe adverse drug effects. Logistic regression models were estimated to determine potential risk factors associated with exposure to the interaction pairs.

Results

A total of 6,417 (23%) patients were exposed to 14,213 potentially harmful interactions; 4,725 patients had at least one exposure from the same pharmacy, and 4,032 patients were exposed by the same physician. The greatest number of exposures (N=1,353) to potentially harmful combinations involved olanzapine and haloperidol. Patients prescribed risperidone were most likely to be exposed to an interaction (13.1%), followed by patients prescribed olanzapine (10.3%), quetiapine (3.3%), and clozapine (3.2%). A higher risk of exposure was associated with being female (odds ratio [OR]=.94), being white (OR=1.43), having depression (OR=1.21), or having impulse-control disorder (OR=1.98).

Conclusions

Interventions by physicians and pharmacies to reduce the prescribing and dispensing of potentially harmful pairs of medications to patients with schizophrenia are recommended.

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Information & Authors

Information

Published In

Go to Psychiatric Services
Go to Psychiatric Services
Cover: Untitled, by Robert Rauschenberg, 1963. Oil, silkscreened ink, metal, and plastic on canvas; 82 × 48 × 6¼ inches. Solomon R. Guggenheim Museum, New York, purchased with funds contributed by Elaine and Werner Dannheisser and the Dannheisser Foundation (82.2912).
Psychiatric Services
Pages: 1080 - 1088
PubMed: 22910806

History

Published online: 1 November 2012
Published in print: November 2012

Authors

Details

Jeff Jianfei Guo, B.Pharm., Ph.D.
Jasmanda Wu, M.P.H., Ph.D.
Christina M. L. Kelton, Ph.D.
Nick C. Patel, Pharm.D., Ph.D.
Dr. Guo is affiliated with the Division of Pharmacy Practice and Administrative Sciences, College of Pharmacy, University of Cincinnati Medical Center, 3225 Eden Ave., Cincinnati, OH 45267 (e-mail: [email protected]).
Dr. Wu is with the Department of Epidemiology and Drug Safety, Bristol-Myers Squibb Company, Princeton, New Jersey.
Dr. Kelton is with the College of Business, University of Cincinnati, Ohio.
Dr. Jing is with the Department of Health Economics and Outcomes Research, Bristol-Myers Squibb.
Mr. Fan is with the Department of Biostatistics and Epidemiology, College of Medicine, University of Cincinnati.
Dr. Keck is with the Department of Psychiatry, College of Medicine, University of Cincinnati.
Dr. Patel is with LifeSynch, Fort Worth, Texas.

Notes

This study was presented at the annual meetings of the American Psychiatric Association, Washington, D.C., May 3–8, 2008, and of the International Society for Pharmacoeconomics and Outcomes Research, Toronto, Ontario, Canada, May 3–7, 2008.

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