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Pariente A, Fourrier-Réglat A, Ducruet T, et al. Antipsychotic Use and Myocardial Infarction in Older Patients With Treated Dementia. Arch Intern Med. 2012;172(8):648–653. doi:10.1001/archinternmed.2012.28
Author Affiliations: Faculty of Pharmacy, Université de Montreal (Drs Pariente and Moride and Mr Ducruet), and Pharmacoepidemiology Unit, Research Center, University of Montréal Hospital Center (Dr Moride, Mr Ducruet, and Ms Béland), Montreal, Quebec, Canada; Unité 657 (Drs Pariente, Moride, Moore, and Fourrier-Réglat) and Unité 897 (Dr Dartigues), Institut National de la Santé et de la Récherche Médicale, Université Bordeaux Ségalen, and Centre Hospitalier Universitaire de Bordeaux, Pharmacology (Drs Pariente, Moore, and Fourrier-Réglat) and Neurology (Dr Dartigues) Departments, Bordeaux, France; and Department of Mathematics and Statistics, The Open University, Milton Keynes, England (Dr Farrington).
Background Antipsychotic agents (APs) are commonly prescribed to older patients with dementia. Antipsychotic use is associated with an increased risk of ischemic stroke in this population. Our study aimed to investigate the association of AP use with the risk of acute myocardial infarction (MI).
Methods A retrospective cohort of community-dwelling older patients who initiated cholinesterase inhibitor treatment was identified between January 1, 2000, and December 31, 2009, using the Quebec, Canada, prescription claims database. From this source cohort, all new AP users during the study period were matched with a random sample of AP nonusers. The risk of MI was evaluated using Cox proportional hazards models, adjusting for age, sex, cardiovascular risk factors, psychotropic drug use, and propensity scores. In addition, a self-controlled case series study using conditional Poisson regression modeling was conducted.
Results Among the source cohort of 37 138 cholinesterase inhibitor users, 10 969 (29.5%) initiated AP treatment. Within 1 year of initiating AP treatment, 1.3% of them had an incident MI. Hazard ratios for the risk of MI after initiation of AP treatment were 2.19 (95% CI, 1.11-4.32) for the first 30 days, 1.62 (95% CI, 0.99-2.65) for the first 60 days, 1.36 (95% CI, 0.89-2.08) for the first 90 days, and 1.15 (95% CI, 0.89-1.47) for the first 365 days. The self-controlled case series study conducted among 804 incident cases of MI among new AP users yielded incidence rate ratios of 1.78 (95% CI, 1.26-2.52) for the 1- to 30-day period, 1.67 (95% CI, 1.09-2.56) for the 31- to 60-day period, and 1.37 (95% CI, 0.82-2.28) for the 61- to 90-day period.
Conclusion Antipsychotic use is associated with a modest and time-limited increase in the risk of MI among community-dwelling older patients treated with cholinesterase inhibitors.
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