Abstract

BackgroundMyocardial infarction (MI) is associated with high morbidity and mortality, particularly in the first 12 months post-event. Interventions such as dual antiplatelet therapy can reduce the risk of major adverse cardiovascular events (MACE), but the duration of the high-risk time interval and the optimal prescription time frame for these interventions remains unknown.Design, setting, participants, and measurementsWe performed a retrospective cohort study using data from medical services and hospitalizations in Manitoba, Canada for patients admitted with a MI between April 2006 and March 2010, and followed until Nov 30, 2014. We used survival analysis to determine the cumulative incidence of death, subsequent MI, or stroke, and used Cox proportional hazards models to assess factors associated with these endpoints.ResultsThere were 8,493 patients in Manitoba admitted to hospital for a MI during the study period. Of those, 6,749 (79.5%) survived for at least 1 year without a recurrent MI or stroke. In the following year, this population remained at high risk, with 372 (5.5%) of the remaining patients dying in the next twelve months (48.1% cardiovascular deaths), 244 (3.6%) having a recurrent MI, and 74 (1.1%) having a stroke. Older age, male sex, diabetes, prior stroke, prior heart failure, prior unstable angina, and absence of revascularization were associated with worse long-term prognosis.ConclusionsThe risk of MACE remains elevated among post-MI patients after the first year. Interventions to more intensively monitor, evaluate, and treat these patients should be considered beyond the first year following myocardial infarction.

Highlights

  • Cardiovascular (CV) disease causes one-third of deaths in Canada, more than any other illness, and is associated with a high economic burden on the health care system [1]

  • Myocardial infarction (MI) is associated with high morbidity and mortality, in the first 12 months post-event. Interventions such as dual antiplatelet therapy can reduce the risk of major adverse cardiovascular events (MACE), but the duration of the high-risk time interval and the optimal prescription time frame for these interventions remains unknown

  • The risk of MACE remains elevated among post-MI patients after the first year

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Summary

Introduction

Cardiovascular (CV) disease causes one-third of deaths in Canada, more than any other illness, and is associated with a high economic burden on the health care system [1]. Despite improvements in acute therapy, and better risk factor control, recurrence rates of major adverse cardiovascular events (MACE), including MI, stroke, and/or death remain high, affecting nearly 1 in 5 patients in the first year post discharge and another 1 in 5 patients over the 3 years [2,3,4]. Dual antiplatelet therapy (DAPT) is a mainstay of secondary prevention of MACE up to 1 year post-event [7]. Myocardial infarction (MI) is associated with high morbidity and mortality, in the first 12 months post-event. Interventions such as dual antiplatelet therapy can reduce the risk of major adverse cardiovascular events (MACE), but the duration of the high-risk time interval and the optimal prescription time frame for these interventions remains unknown

Methods
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