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Volume 359:1802-1810 October 23, 2008 Number 17
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Cardiovascular Outcomes after a Change in Prescription Policy for Clopidogrel
Cynthia A. Jackevicius, Pharm.D., M.Sc., Jack V. Tu, M.D., Ph.D., Virginie Demers, M.D., Magda Melo, B.Sc.Phm., M.Sc., Jafna Cox, M.D., Stephane Rinfret, M.D., M.Sc., Dimitri Kalavrouziotis, M.D., M.Sc., Helen Johansen, Ph.D., Hassan Behlouli, Ph.D., Alice Newman, M.Sc., and Louise Pilote, M.D., M.P.H., Ph.D.

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ABSTRACT

Background Drug-reimbursement policies may have an adverse effect on patient outcomes if they interfere with timely access to efficacious medications for acute medical conditions. Clopidogrel in combination with aspirin is the recommended standard of care for patients receiving coronary stents to prevent thrombosis. We examined the population-level effect of a change by a Canadian provincial government in a pharmacy-benefits program from a prior-authorization policy to a less restrictive, limited-use policy on access to clopidogrel among patients undergoing percutaneous coronary intervention (PCI) with stenting after acute myocardial infarction.

Methods We conducted a population-based, retrospective, time-series analysis from April 1, 2000, to March 31, 2005, of all patients 65 years of age or older with acute myocardial infarction who underwent PCI with stenting in Ontario, Canada. The primary outcome was the composite rate of death, recurrent acute myocardial infarction, PCI, and coronary-artery bypass grafting at 1 year, with adjustment for sex and age. The secondary outcome was major bleeding.

Results The rate of clopidogrel use within 30 days after hospital discharge following myocardial infarction increased from 35% in the prior-authorization period to 88% in the limited-use period. The median time to the first dispensing of a clopidogrel prescription decreased from 9 days in the first period to 0 days in the second period. The 1-year composite cardiovascular outcome significantly decreased from 15% in the prior-authorization group to 11% in the limited-use group (P=0.02). Rates of bleeding in the two groups did not change.

Conclusions The removal of a prior-authorization program led to improvement in timely access to clopidogrel for coronary stenting and improved cardiovascular outcomes.


Source Information

From the Western University of Health Sciences, Pomona, CA (C.A.J.); the University of Toronto (C.A.J., J.V.T.), the University Health Network (C.A.J.), the Institute for Clinical Evaluative Sciences (C.A.J., J.V.T., M.M., A.N.), and Sunnybrook Health Sciences Centre (J.V.T.) — all in Toronto; McGill University Health Centre (V.D., H.B., L.P.) and the University of Montreal (S.R.) — both in Montreal; Dalhousie University, Halifax, NS, Canada (J.C., D.K.); and Statistics Canada, Ottawa (H.J.).

Address reprint requests to Dr. Jackevicius at Western University of Health Sciences, College of Pharmacy, 309 E. Second St., Pomona, CA 91766, or at cjackevicius{at}westernu.edu.

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