Uppsala Clinical Research Center, Department of Medical Sciences, Uppsala University, Sweden.
J Am Coll Cardiol. 2011 Feb 8;57(6):672-84. doi: 10.1016/j.jacc.2010.10.029. Epub 2010 Dec 30.
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.
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.
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.
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.
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.
本研究旨在评估替格瑞洛和氯吡格雷在接受冠状动脉旁路移植术(CABG)的急性冠状动脉综合征患者中的疗效和安全性,作为随机分组后的策略。
替格瑞洛是一种新型、可逆结合的、口服、直接作用的 P2Y(12)受体拮抗剂。在 PLATO(血小板抑制和患者结局)试验中,18624 例急性冠状动脉综合征患者随机分组,替格瑞洛与氯吡格雷相比,显著降低了心血管(CV)死亡、心肌梗死或卒中的主要复合终点风险(风险比[HR]:0.84;95%置信区间[CI]:0.77 至 0.92;p<0.001)。本报告调查了接受试验期间 CABG 治疗的患者的结局。
共有 1899 例患者在随机分组后接受 CABG。方案建议替格瑞洛/安慰剂在 24 至 72 小时内停药,氯吡格雷/安慰剂在术前 5 天停药。共有 1261 例患者接受 CABG 且在术前<7 天接受研究药物治疗。统计分析基于从 CABG 手术开始到研究结束的事件,不包括 3 例在研究结束后接受 CABG 的患者。
在 1261 例患者队列中,12 个月时主要复合终点的相对减少率为 10.6%(629 例中的 66 例用替格瑞洛治疗)和 13.1%(629 例中的 79 例用氯吡格雷治疗)(HR:0.84;95%CI:0.60 至 1.16;p=0.29),与整个试验的结果一致。总死亡率从 9.7%(629 例中的 58 例)降至 4.7%(629 例中的 29 例)(HR:0.49;95%CI:0.32 至 0.77;p<0.01),CV 死亡率从 7.9%(629 例中的 47 例)降至 4.1%(629 例中的 25 例)(HR:0.52;95%CI:0.32 至 0.85;p<0.01),非 CV 死亡率从 2.0%降至 0.7%(p=0.07)。随机治疗之间在 CABG 相关大出血方面无显著差异。
在最后一次研究药物摄入后 7 天内接受 CABG 的患者亚组中,替格瑞洛与氯吡格雷相比,总死亡率和 CV 死亡率显著降低,且无 CABG 相关出血的风险增加。