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替格瑞洛联合阿司匹林、替格瑞洛单药或阿司匹林单药对冠状动脉旁路移植术后 1 年大隐静脉桥通畅率的影响:一项随机临床试验。

Effect of Ticagrelor Plus Aspirin, Ticagrelor Alone, or Aspirin Alone on Saphenous Vein Graft Patency 1 Year After Coronary Artery Bypass Grafting: A Randomized Clinical Trial.

机构信息

Ruijin Hospital Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Changhai Hospital of Shanghai, Shanghai, China.

出版信息

JAMA. 2018 Apr 24;319(16):1677-1686. doi: 10.1001/jama.2018.3197.

Abstract

IMPORTANCE

The effect of ticagrelor with or without aspirin on saphenous vein graft patency in patients undergoing coronary artery bypass grafting (CABG) is unknown.

OBJECTIVE

To compare the effect of ticagrelor + aspirin or ticagrelor alone vs aspirin alone on saphenous vein graft patency 1 year after CABG.

DESIGN, SETTING, AND PARTICIPANTS: Randomized, multicenter, open-label, clinical trial among 6 tertiary hospitals in China. Eligible patients were aged 18 to 80 years with indications for elective CABG. Patients requiring urgent revascularization, concomitant cardiac surgery, dual antiplatelet or vitamin K antagonist therapy post-CABG, and who were at risk of serious bleeding were excluded. From July 2014 until November 2015, 1256 patients were identified and 500 were enrolled. Follow-up was completed in January 2017.

INTERVENTIONS

Patients were randomized (1:1:1) to start ticagrelor (90 mg twice daily) + aspirin (100 mg once daily) (n = 168), ticagrelor (90 mg twice daily) (n = 166), or aspirin (100 mg once daily) (n = 166) within 24 hours post-CABG. Neither patients nor treating physicians were blinded to allocation.

MAIN OUTCOMES AND MEASURES

Primary outcome was saphenous vein graft patency 1 year after CABG (FitzGibbon grade A) adjudicated independently by a committee blinded to allocation. Saphenous vein graft patency was assessed by multislice computed tomographic angiography or coronary angiography.

RESULTS

Among 500 randomized patients (mean age, 63.6 years; women, 91 [18.2%]), 461 (92.2%) completed the trial. Saphenous vein graft patency rates 1 year post-CABG were 88.7% (432 of 487 vein grafts) with ticagrelor + aspirin; 82.8% (404 of 488 vein grafts) with ticagrelor alone; and 76.5% (371 of 485 vein grafts) with aspirin alone. The difference between ticagrelor + aspirin vs aspirin alone was statistically significant (12.2% [95% CI, 5.2% to 19.2%]; P < .001), whereas the difference between ticagrelor alone vs aspirin alone was not statistically significant (6.3% [95% CI, -1.1% to 13.7%]; P = .10). Five major bleeding episodes occurred during 1 year of follow-up (3 with ticagrelor + aspirin; 2 with ticagrelor alone).

CONCLUSIONS AND RELEVANCE

Among patients undergoing elective CABG with saphenous vein grafting, ticagrelor + aspirin significantly increased graft patency after 1 year vs aspirin alone; there was no significant difference between ticagrelor alone and aspirin alone. Further research with more patients is needed to assess comparative bleeding risks.

TRIAL REGISTRATION

clinicaltrials.gov Identifier: NCT02201771.

摘要

重要性

替格瑞洛联合或不联合阿司匹林对行冠状动脉旁路移植术(CABG)患者的隐静脉桥通畅率的影响尚不清楚。

目的

比较替格瑞洛+阿司匹林与替格瑞洛单药或阿司匹林单药治疗 1 年后隐静脉桥通畅率的差异。

设计、地点和参与者:这是一项在中国 6 家三级医院进行的随机、多中心、开放标签临床试验。纳入标准为年龄 18 至 80 岁,有择期 CABG 适应证的患者。需要紧急血运重建、同期心脏手术、CABG 后双联抗血小板或维生素 K 拮抗剂治疗以及有严重出血风险的患者被排除在外。2014 年 7 月至 2015 年 11 月,共确定了 1256 名患者,其中 500 名符合条件的患者入组。随访于 2017 年 1 月完成。

干预

患者在术后 24 小时内随机(1:1:1)接受替格瑞洛(90 mg,每日 2 次)+阿司匹林(100 mg,每日 1 次)(n=168)、替格瑞洛(90 mg,每日 2 次)(n=166)或阿司匹林(100 mg,每日 1 次)(n=166)治疗。患者和治疗医生均不知道分组情况。

主要终点和测量指标

主要终点是 1 年后 CABG 后隐静脉桥通畅率(FitzGibbon 分级 A),由对分组情况设盲的委员会独立判定。隐静脉桥通畅率通过多层螺旋 CT 血管造影或冠状动脉造影评估。

结果

在 500 名随机分组的患者(平均年龄 63.6 岁;女性 91 例[18.2%])中,461 名(92.2%)完成了试验。CABG 术后 1 年时,替格瑞洛+阿司匹林组隐静脉桥通畅率为 88.7%(432 根静脉桥);替格瑞洛组为 82.8%(404 根静脉桥);阿司匹林组为 76.5%(371 根静脉桥)。替格瑞洛+阿司匹林组与阿司匹林组相比差异有统计学意义(12.2%[95%CI,5.2%至 19.2%];P<0.001),而替格瑞洛组与阿司匹林组之间差异无统计学意义(6.3%[95%CI,-1.1%至 13.7%];P=0.10)。在 1 年的随访期间,共发生 5 例大出血事件(替格瑞洛+阿司匹林组 3 例,替格瑞洛组 2 例)。

结论和相关性

在接受择期 CABG 并伴有隐静脉桥移植术的患者中,与阿司匹林单药相比,替格瑞洛+阿司匹林可显著增加术后 1 年的桥通畅率;替格瑞洛单药与阿司匹林单药之间无显著差异。还需要更多的患者来评估比较出血风险。

试验注册

clinicaltrials.gov 标识符:NCT02201771。

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