Title of article :
Ticagrelor Versus Clopidogrel in Patients With Acute Coronary Syndromes Undergoing Coronary Artery Bypass Surgery: Results From the PLATO (Platelet Inhibition and Patient Outcomes) Trial
Author/Authors :
Held، نويسنده , , Claes and إsenblad، نويسنده , , Nils and Bassand، نويسنده , , Jean Pierre and Becker، نويسنده , , Richard C. and Cannon، نويسنده , , Christopher P. and Claeys، نويسنده , , Marc J. and Harrington، نويسنده , , Robert A. and Horrow، نويسنده , , Jay and Husted، نويسنده , , Steen and James، نويسنده , , Stefan K. and Mahaffey، نويسنده , , Kenneth W. and Nicolau، نويسنده , , José C. and Scirica، نويسنده , , Benjamin M. and Storey، نويسنده , , Robert F. and Vintila، نويسنده , , Marius and Ycas، نويسنده , , Joseph and Wallentin، نويسنده , , Lars، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2011
Pages :
13
From page :
672
To page :
684
Abstract :
Objectives rpose 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. ound elor is a novel, reversibly binding, oral, direct-acting P2Y12-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. s al, 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. s 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. sions 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.
Keywords :
Clopidogrel , acute coronary syndromes , Coronary Artery Bypass Grafting , Ticagrelor
Journal title :
JACC (Journal of the American College of Cardiology)
Serial Year :
2011
Journal title :
JACC (Journal of the American College of Cardiology)
Record number :
1749056
Link To Document :
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