Rationale and design of The Intracoronary Stenting and Antithrombotic Regimen-Testing of a six-week versus a six-month clopidogrel treatment Regimen In Patients with concomitant aspirin and oraL anticoagulant therapy following drug-Eluting stenting (ISAR-TRIPLE) study

被引:17
作者
Fiedler, K. Anette [1 ,2 ]
Byrne, Robert A. [1 ,2 ]
Schulz, Stefanie [1 ]
Sibbing, Dirk [3 ]
Mehilli, Julinda [2 ,3 ]
Ibrahim, Tareq [4 ]
Maeng, Michael [5 ]
Laugwitz, Karl-Ludwig [4 ]
Kastrati, Adnan [1 ,2 ]
Sarafoff, Nikolaus [2 ,3 ]
机构
[1] Tech Univ Munich, Deutsch Herzzentrum, D-80290 Munich, Germany
[2] DZHK German Ctr Cardiovasc Res, Partner Site Munich Heart Alliance, Munich, Germany
[3] Klinikum Ludwig Maximilians Univ, Munich, Germany
[4] Tech Univ Munich, Klinikum Rechts Isar, Med Klin 1, D-80290 Munich, Germany
[5] Aarhus Univ Hosp, Dept Cardiol, DK-8000 Aarhus, Denmark
关键词
PERCUTANEOUS CORONARY INTERVENTION; VITAMIN-K ANTAGONISTS; ATRIAL-FIBRILLATION; EUROPEAN-SOCIETY; LONG-TERM; MYOCARDIAL-INFARCTION; ANTIPLATELET THERAPY; TASK-FORCE; IMPLANTATION; PREVENTION;
D O I
10.1016/j.ahj.2014.01.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background An increasing number of patients undergoing coronary stenting need lifelong anticoagulation and therefore require a triple therapy typically consisting of aspirin, clopidogrel, and a vitamin K antagonist. Triple therapy confers an elevated bleeding risk as compared with dual therapy; however, omission of either antiplatelet or anticoagulation therapy might increase the risk of stent thrombosis or thrombembolic events. Although guidelines recommend a duration of dual antiplatelet therapy of 6 to 12 months after drug-eluting stent (DES) implantation, the optimal duration of dual antiplatelet therapy in patients receiving oral anticoagulation is not known. Hypothesis We postulate that 6-week clopidogrel therapy after DES implantation as compared with 6-month therapy is associated with improved clinical outcomes in patients undergoing DES implantation receiving concomitant aspirin and vitamin K antagonists. Study design The ISAR-TRIPLE is a randomized, open- label trial that examines the restriction of clopidogrel therapy from 6 months to 6 weeks after DES implantation in the setting of concomitant aspirin and oral anticoagulant. Patients are randomized in a 1: 1 fashion to either 6-week or 6-month clopidogrel therapy. The primary end point is a composite of death, myocardial infarction, definite stent thrombosis, stroke, or major bleeding. The secondary end point comprises ischemic and bleeding complications. According to sample size calculations, a total of 600 patients are required to be enrolled. Clinical follow-up is scheduled at 6 weeks and at 6 and 9 months after randomization. Summary There is clinical equipoise regarding the optimal duration of triple therapy after DES implantation in patients who need vitamin K antagonist therapy. The ISAR-TRIPLE trial aims to test the hypothesis that a 6-week triple therapy compared with a 6-month triple therapy improves net clinical outcomes.
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收藏
页码:459 / U66
页数:8
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