Key result
Compared to dual antiplatelets, clopidogrel plus warfarin was associated with a lower risk of cardiovascular outcomes at 91-365 days (HR 0.68; 95% CI 0.49-0.95) without higher major bleeding risk.
Why the study?
Do different antithrombotic regimes (triple therapy, aspirin plus warfarin, clopidogrel plus warfarin) improve cardiovascular outcomes and reduce major bleeds compared to dual antiplatelet therapy in patients with myocardial infarction and atrial fibrillation undergoing PCI?
Cohort (n=7,116)
Yes
Do different antithrombotic regimes (triple therapy, aspirin plus warfarin, clopidogrel plus warfarin) improve cardiovascular outcomes and reduce major bleeds compared to dual antiplatelet therapy in patients with myocardial infarction and atrial fibrillation undergoing PCI?
Effect estimate: HR 0.68 (95% CI 0.49-0.95)
In patients with MI and AF undergoing PCI, dual therapy with warfarin and a single antiplatelet (aspirin or clopidogrel) is associated with better long-term cardiovascular outcomes and less bleeding compared to dual antiplatelet therapy or triple therapy.
May support clopidogrel plus warfarin long-term in MI-AF post-PCI; leaves open randomized confirmation before practice change.
Aims: Optimal antithrombotic therapy after percutaneous coronary intervention (PCI) in patients with myocardial infarction (MI) and atrial fibrillation is uncertain. In this study, we compared antithrombotic regimes with regard to a composite cardiovascular outcome of all-cause mortality, MI or ischaemic stroke, and major bleeds. Methods and results: Patients between October 2005 and December 2012 were identified in Swedish registries, n = 7116. Landmark 0-90 and 91-365 days of outcome were evaluated with Cox-regressions, with dual antiplatelet therapy as reference. At discharge, 16.2% received triple therapy (aspirin, clopidogrel, and warfarin), 1.9% aspirin plus warfarin, 7.3% clopidogrel plus warfarin, and 60.8% dual antiplatelets. For cardiovascular outcome, adjusted hazard ratio with 95% confidence interval (HR) for triple therapy was 0.86 (0.70-1.07) for 0-90 days and 0.78 (0.58-1.05) for 91-365 days. A HR of 2.16 (1.48-3.13) and 1.61 (0.98-2.66) during 0-90 and 91-365 days, respectively, was observed for major bleeds. For aspirin plus warfarin, HR 0.82 (0.54-1.26) and 0.62 (0.48-0.79) was observed for cardiovascular outcome and 1.30 (0.60-2.85) and 1.01 (0.63-1.62) for major bleeds during 0-90 and 91-365 days, respectively. For clopidogrel plus warfarin, HR of 0.90 (0.68-1.19) and 0.68 (0.49-0.95) was observed for cardiovascular outcome and 1.28 (0.71-2.32) and 1.08 (0.57-2.04) for major bleeds during 0-90 and 91-365 days, respectively. Conclusion: Compared to dual antiplatelets, aspirin or clopidogrel plus warfarin therapy was associated with similar 0-90 days and lower 91-365 days of risk of the cardiovascular outcome, without higher risk of major bleeds. Triple therapy was associated with non-significant lower risk of cardiovascular outcome and higher risk of major bleeds.
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Batra et al. (2017) conducted a cohort in Myocardial infarction and atrial fibrillation (n=7,116). Triple therapy, aspirin plus warfarin, or clopidogrel plus warfarin vs. Dual antiplatelet therapy was evaluated on Composite cardiovascular outcome of all-cause mortality, MI or ischaemic stroke (HR 0.68, 95% CI 0.49-0.95). Compared to dual antiplatelets, clopidogrel plus warfarin was associated with a lower risk of cardiovascular outcomes at 91-365 days (HR 0.68; 95% CI 0.49-0.95) without higher major bleeding risk.
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