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多血管病变行 CABG 的糖尿病患者中双联抗血小板治疗与阿司匹林单药治疗的比较:FREEDOM 研究结果。

Dual Antiplatelet Therapy Versus Aspirin Monotherapy in Diabetics With Multivessel Disease Undergoing CABG: FREEDOM Insights.

机构信息

Department of Critical Care and Division of Cardiology, University of Alberta, Edmonton, Alberta, Canada; Canadian VIGOUR Centre, University of Alberta, Edmonton, Alberta, Canada.

Icahn School of Medicine at Mount Sinai, New York, New York.

出版信息

J Am Coll Cardiol. 2017 Jan 17;69(2):119-127. doi: 10.1016/j.jacc.2016.10.043.

Abstract

BACKGROUND

Clinical practice guidelines recommend post-operative dual antiplatelet therapy (DAPT) in patients who undergo coronary artery bypass grafting (CABG) following acute coronary syndromes (ACS).

OBJECTIVES

The authors have evaluated DAPT utilization rates and associated outcomes among post-CABG patients with diabetes.

METHODS

In a post hoc, nonrandomized analysis from the FREEDOM (Future REvascularization Evaluation in patients with Diabetes mellitus: Optimal management of Multivessel disease) trial, we compared patients receiving DAPT (aspirin plus thienopyridine) and aspirin monotherapy at 30 days post-operatively. The primary outcome was the risk adjusted 5-year FREEDOM composite of all-cause mortality, nonfatal myocardial infarction, or stroke. Safety outcomes included major bleeding, blood transfusion, and hospitalization for bleeding.

RESULTS

At 30 days post-CABG, 544 (68.4%) patients received DAPT and 251 (31.6%) patients received aspirin alone. The median (25th, 75th percentile) duration of clopidogrel therapy was 0.98 (0.23 to 1.91) years. There was no significant difference in the 5-year primary composite outcome between DAPT- and aspirin-treated patients (12.6% vs. 16.0%; adjusted hazard ratio [HR]: 0.83; 95% confidence interval [CI]: 0.54 to 1.27; p = 0.39). The 5-year primary composite outcomes were similar for patients receiving DAPT versus aspirin monotherapy respectively, in subgroups with pre-CABG ACSs (15.2% vs. 16.5%; HR: 1.06; 95% CI: 0.53 to 2.10; p = 0.88) and those with stable angina (11.6% vs. 15.8%; HR: 0.82; 95% CI: 0.50 to 1.343; p = 0.42). The composite outcomes of both treatment groups were also similar by SYNTAX score, duration of DAPT therapy, completeness of revascularization, and in off-pump CABG. No treatment-related differences in major bleeding (5.6% vs. 5.7%; HR: 1.00; 95% CI: 0.50 to 1.99; p = 0.99), blood transfusions (4.8% vs. 4.5%; HR: 1.09; 95% CI: 0.51 to 2.34; p = 0.82), or hospitalization for bleeding (2.6% vs. 3.3%; HR: 0.85; 95% CI: 0.34 to 2.17; p = 0.74) were observed between aspirin- and DAPT-treated patients, respectively.

CONCLUSIONS

The use of DAPT in patients with diabetes post-CABG in our cohort was high. Compared with aspirin monotherapy, no associated differences were observed in cardiovascular or bleeding outcomes, suggesting that routine use of DAPT may not be clinically warranted. (Future REvascularization Evaluation in patients with Diabetes mellitus: Optimal management of Multivessel disease [FREEDOM]; NCT00086450).

摘要

背景

临床实践指南建议,在急性冠脉综合征(ACS)后接受冠状动脉旁路移植术(CABG)的患者术后应进行双联抗血小板治疗(DAPT)。

目的

作者评估了合并糖尿病的 CABG 术后患者的 DAPT 使用率及其相关结局。

方法

在 FREEDOM(糖尿病患者的未来血运重建评估:多血管病变的最佳治疗)试验的事后、非随机分析中,我们比较了术后 30 天接受 DAPT(阿司匹林加噻吩吡啶)和阿司匹林单药治疗的患者。主要结局是风险调整的 5 年 FREEDOM 复合终点,包括全因死亡率、非致死性心肌梗死或卒中。安全性结局包括大出血、输血和出血住院。

结果

在 CABG 术后 30 天,544 例(68.4%)患者接受 DAPT,251 例(31.6%)患者接受阿司匹林单药治疗。氯吡格雷治疗的中位(25 分位,75 分位)持续时间为 0.98 年(0.23 年至 1.91 年)。DAPT 治疗组与阿司匹林治疗组的 5 年主要复合结局无显著差异(12.6% vs. 16.0%;调整后的危险比 [HR]:0.83;95%置信区间 [CI]:0.54 至 1.27;p=0.39)。在分别接受 DAPT 与阿司匹林单药治疗的患者亚组中,包括 CABG 前 ACS(15.2% vs. 16.5%;HR:1.06;95%CI:0.53 至 2.10;p=0.88)和稳定型心绞痛(11.6% vs. 15.8%;HR:0.82;95%CI:0.50 至 1.34;p=0.42)患者中,5 年主要复合结局相似。两组治疗的复合结局在 SYNTAX 评分、DAPT 治疗持续时间、血运重建的完整性和非体外循环 CABG 中也相似。阿司匹林和 DAPT 治疗组之间未观察到大出血(5.6% vs. 5.7%;HR:1.00;95%CI:0.50 至 1.99;p=0.99)、输血(4.8% vs. 4.5%;HR:1.09;95%CI:0.51 至 2.34;p=0.82)或出血住院(2.6% vs. 3.3%;HR:0.85;95%CI:0.34 至 2.17;p=0.74)的治疗相关差异。

结论

我们队列中 CABG 术后合并糖尿病患者 DAPT 的使用率较高。与阿司匹林单药治疗相比,心血管或出血结局无相关差异,这表明常规使用 DAPT 可能在临床上没有必要。(糖尿病患者的未来血运重建评估:多血管病变的最佳治疗 [FREEDOM];NCT00086450)。

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