Ticagrelor Versus Clopidogrel in Patients With Acute Coronary Syndromes Undergoing Coronary Artery Bypass Surgery Results From the PLATO (Platelet Inhibition and Patient Outcomes) Trial

被引:420
作者
Held, Claes [1 ,2 ]
Asenblad, Nils [2 ]
Bassand, Jean Pierre [3 ]
Becker, Richard C. [4 ]
Cannon, Christopher P. [5 ]
Claeys, Marc J. [6 ]
Harrington, Robert A. [4 ]
Horrow, Jay [7 ]
Husted, Steen [8 ]
James, Stefan K. [2 ]
Mahaffey, Kenneth W. [4 ]
Nicolau, Jose C. [9 ]
Scirica, Benjamin M. [5 ]
Storey, Robert F. [10 ]
Vintila, Marius [11 ]
Ycas, Joseph [7 ]
Wallentin, Lars [2 ]
机构
[1] Uppsala Univ, Dept Cardiol, Uppsala Clin Res Ctr, S-75185 Uppsala, Sweden
[2] Uppsala Univ, Dept Med Sci, S-75185 Uppsala, Sweden
[3] Univ Besancon, F-25030 Besancon, France
[4] Duke Clin Res Inst, Durham, NC USA
[5] Brigham & Womens Hosp, TIMI Study Grp, Boston, MA 02115 USA
[6] Univ Hosp, Edegem, Belgium
[7] AstraZeneca Res & Dev, Wilmington, DE USA
[8] Arhus Univ Hosp, Aarhus, Denmark
[9] Univ Sao Paolo, Sch Med, Sao Paulo, Brazil
[10] Univ Sheffield, Sheffield, S Yorkshire, England
[11] Carol Davila Univ Med Bucharest, Bucharest, Romania
关键词
acute coronary syndromes; clopidogrel; coronary artery bypass grafting; ticagrelor; ST-SEGMENT ELEVATION; MYOCARDIAL-INFARCTION; GRAFT-SURGERY; ASPIRIN; MANAGEMENT; INTERVENTION; ANTAGONIST; THERAPY; SAFETY; CURE;
D O I
10.1016/j.jacc.2010.10.029
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives The purpose of this study is to evaluate the efficacy and safety of ticagrelor and clopidogrel in patients with acute coronary syndrome undergoing coronary artery bypass graft surgery (CABG), as a post-randomization strategy. Background Ticagrelor is a novel, reversibly binding, oral, direct-acting P2Y(12)-receptor antagonist. In the PLATO (Platelet Inhibition and Patient Outcomes) trial, which randomized 18,624 patients with acute coronary syndromes, ticagrelor compared with clopidogrel significantly reduced the risk of the primary composite end point of cardiovascular (CV) death, myocardial infarction, or stroke (hazard ratio [HR]: 0.84; 95% confidence interval [CI]: 0.77 to 0.92; p < 0.001). This report investigated the outcomes of patients treated with CABG during the trial. Methods In total, 1,899 patients underwent CABG post-randomization. The protocol recommended ticagrelor/placebo to be withheld for 24 to 72 h and clopidogrel/placebo for 5 days preoperatively. In all, 1,261 patients underwent CABG and were receiving study drug treatment <7 days before surgery. The statistical analysis was based on events occurring from the CABG procedure until the end of the study, excluding 3 patients with CABG after study end. Results In the 1,261 patient cohort, the relative reduction of primary composite end point at 12 months (10.6% [66 of 629] with ticagrelor versus 13.1% [79 of 629] with clopidogrel; HR: 0.84; 95% CI: 0.60 to 1.16; p = 0.29) was consistent with the results of the whole trial. Total mortality was reduced from 9.7% (58 of 629) to 4.7% (29 of 629; HR: 0.49; 95% CI: 0.32 to 0.77; p < 0.01), CV death from 7.9% (47 of 629) to 4.1% (25 of 629; HR: 0.52; 95% CI: 0.32 to 0.85; p < 0.01), and non-CV death numerically from 2.0% to 0.7% (p = 0.07). There was no significant difference in CABG-related major bleeding between the randomized treatments. Conclusions In the subgroup of patients undergoing CABG within 7 days after the last study drug intake, ticagrelor compared with clopidogrel was associated with a substantial reduction in total and CV mortality without excess risk of CABG-related bleeding. (J Am Coll Cardiol 2011;57:672-84) (C) 2011 by the American College of Cardiology Foundation
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收藏
页码:672 / 684
页数:13
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