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首页> 外文期刊>Journal of the American College of Cardiology >Ticagrelor versus clopidogrel in patients with acute coronary syndromes undergoing coronary artery bypass surgery: results from the PLATO (Platelet Inhibition and Patient Outcomes) trial.
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Ticagrelor versus clopidogrel in patients with acute coronary syndromes undergoing coronary artery bypass surgery: results from the PLATO (Platelet Inhibition and Patient Outcomes) trial.

机译:替加格雷洛与氯吡格雷在接受冠状动脉搭桥手术的急性冠脉综合征患者中的应用:PLATO(血小板抑制和患者预后)试验的结果。

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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.
机译:目的:本研究的目的是评估替卡格雷和氯吡格雷在接受冠状动脉搭桥术(CABG)的急性冠状动脉综合征患者中的疗效和安全性,作为一种随机后的策略。背景:替卡格雷是一种新颖的,可逆结合的口服直接作用的P2Y(12)-受体拮抗剂。在PLATO(血小板抑制和患者预后)试验中,对18,624例急性冠脉综合征患者进行了随机分组,与替加格雷相比,替卡格雷或氯吡格雷显着降低了心血管(CV)死亡,心肌梗塞或中风的主要复合终点风险(危险比) [HR]:0.84; 95%置信区间[CI]:0.77至0.92; p <0.001)。该报告调查了在试验期间接受CABG治疗的患者的结局。方法:总共1,899例患者在随机化后接受了CABG。该方案建议术前停用替卡格雷/安慰剂24至72小时,停用氯吡格雷/安慰剂5天。共有1,261例患者接受了CABG,并在手术前不到7天接受了研究药物治疗。统计分析基于从CABG手术到研究结束的事件,研究结束后不包括3例CABG患者。结果:在1,261名患者队列中,主要复合终点在12个月时相对减少(替卡格雷治疗组为10.6%[629的66],氯吡格雷治疗组为13.1%[629的79]; 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的58)降低到4.7%(629的29; HR:0.49; 95%CI:0.32到0.77; p <0.01),CV死亡率从7.9%(629的47)降低到4.1% (629之25; HR:0.52; 95%CI:0.32至0.85; p <0.01),非CV死亡数值从2.0%至0.7%(p = 0.07)。在随机治疗之间,CABG相关的主要出血没有显着差异。结论:在最后一次研究药物摄入后7天内接受CABG治疗的患者亚组中,替卡格雷与氯吡格雷相比可显着降低总死亡率和CV死亡率,且不会增加CABG相关出血的风险。

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