Oral Anticoagulation and Antiplatelets in Atrial Fibrillation Patients After Myocardial Infarction and Coronary Intervention

被引:294
作者
Lamberts, Morten [1 ,2 ]
Gislason, Gunnar H. [1 ,3 ,4 ]
Olesen, Jonas Bjerring [1 ]
Kristensen, Soren Lund [1 ]
Olsen, Anne-Marie Schjerning [1 ]
Mikkelsen, Anders [1 ]
Christensen, Christine Benn [1 ]
Lip, Gregory Y. H. [2 ]
Kober, Lars [5 ]
Torp-Pedersen, Christian [1 ,6 ]
Hansen, Morten Lock [1 ]
机构
[1] Univ Copenhagen, Gentofte Hosp, Dept Cardiol, DK-2900 Hellerup, Denmark
[2] Univ Birmingham, Ctr Cardiovasc Sci, City Hosp, Birmingham, W Midlands, England
[3] Univ Copenhagen, Fac Hlth & Med Sci, Copenhagen, Denmark
[4] Univ Southern Denmark, Natl Inst Publ Hlth, Copenhagen, Denmark
[5] Rigshosp, Copenhagen Univ Hosp, Ctr Heart, Dept Cardiol, DK-2100 Copenhagen, Denmark
[6] Aalborg Univ, Inst Hlth Sci & Technol, Aalborg, Denmark
关键词
antithrombotic treatment; atrial fibrillation; bleeding; myocardial infarction; stroke; NORTH-AMERICAN PERSPECTIVE; LONG-TERM ANTICOAGULATION; RE-LY TRIAL; ANTITHROMBOTIC THERAPY; CONSENSUS DOCUMENT; TRIPLE THERAPY; NATIONWIDE COHORT; EUROPEAN-SOCIETY; SYNDROME AND/OR; WORKING GROUP;
D O I
10.1016/j.jacc.2013.05.029
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The purpose of this study was to investigate the risk of thrombosis and bleeding according to multiple antithrombotic treatment regimens in atrial fibrillation (AF) patients after myocardial infarction (MI) or percutaneous coronary intervention (PCI). Background The optimal antithrombotic treatment strategy is unresolved in patients with multiple indications. Methods A total of 12,165 AF patients hospitalized with MI and/or undergoing PCI between 2001 and 2009 were identified by nationwide registries (60.7% male; mean age 75.6 years). Risk of MI/coronary death, ischemic stroke, and bleeding according to antithrombotic treatment regimen was estimated by Cox regression models. Results Within 1 year, MI or coronary death, ischemic stroke, and bleeding events occurred in 2,255 patients (18.5%), 680 (5.6%), and 769 (6.3%), respectively. Relative to triple therapy (oral anticoagulation [OAC] plus aspirin plus clopidogrel), no increased risk of recurrent coronary events was seen for OAC plus clopidogrel (hazard ratio [HR]: 0.69, 95% confidence interval [CI]: 0.48 to 1.00), OAC plus aspirin (HR: 0.96, 95% CI: 0.77 to 1.19), or aspirin plus clopidogrel (HR: 1.17, 95% CI: 0.96 to 1.42), but aspirin plus clopidogrel was associated with a higher risk of ischemic stroke (HR: 1.50, 95% CI: 1.03 to 2.20). Also, OAC plus aspirin and aspirin plus clopidogrel were associated with a significant increased risk of all-cause death (HR: 1.52, 95% CI: 1.17 to 1.99 and HR: 1.60, 95% CI: 1.25 to 2.05, respectively). When compared to triple therapy, bleeding risk was nonsignificantly lower for OAC plus clopidogrel (HR: 0.78, 95% CI: 0.55 to 1.12) and significantly lower for OAC plus aspirin and aspirin plus clopidogrel. Conclusions In real-life AF patients with indication for multiple antithrombotic drugs after MI/PCI, OAC and clopidogrel was equal or better on both benefit and safety outcomes compared to triple therapy. (C) 2013 by the American College of Cardiology Foundation
引用
收藏
页码:981 / 989
页数:9
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