Aspirin Monotherapy vs No Antiplatelet Therapy in Stable Patients With Coronary Stents Undergoing Low-to-Intermediate Risk Noncardiac Surgery

IF 22.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of the American College of Cardiology Pub Date : 2024-08-31 DOI:10.1016/j.jacc.2024.08.024
Do-Yoon Kang MD , Sang-Hyup Lee MD , Se-Whan Lee MD , Cheol Hyun Lee MD , Choongki Kim MD , Ji-Yong Jang MD , Nihar Mehta MD , Jun-Hyok Oh MD , Young Rak Cho MD , Kyung Ho Yoon MD , Sung Gyun Ahn MD , Jung-Hee Lee MD , Deok-Kyu Cho MD , Yongcheol Kim MD , Jeongsu Kim MD , Gyeong Hun Cho MD , Kyu-Sup Lee MD , Hanbit Park MD , Mutlu Vural MD , Young-Hyo Lim MD , Jae-Hyoung Park
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Abstract

Background

Current guidelines recommend the perioperative continuation of aspirin in patients with coronary drug-eluting stents (DES) undergoing noncardiac surgery. However, supporting evidence is limited.

Objectives

This study aimed to compare continuing aspirin monotherapy vs temporarily holding all antiplatelet therapy before noncardiac surgery in patients with previous DES implantation.

Methods

We randomly assigned patients who had received a DES >1 year previously and were undergoing elective noncardiac surgery either to continue aspirin or to discontinue all antiplatelet agents 5 days before noncardiac surgery. Antiplatelet therapy was recommended to be resumed no later than 48 hours after surgery, unless contraindicated. The primary outcome was a composite of death from any cause, myocardial infarction, stent thrombosis, or stroke between 5 days before and 30 days after noncardiac surgery.

Results

A total of 1,010 patients underwent randomization. Among 926 patients in the modified intention-to-treat population (462 patients in aspirin monotherapy group and 464 patients in the no-antiplatelet therapy group), the primary composite outcome occurred in 3 patients (0.6%) in the aspirin monotherapy group and 4 patients (0.9%) in the no antiplatelet group (difference, −0.2 percentage points; 95% CI: −1.3 to 0.9; P > 0.99). There was no stent thrombosis in either group. The incidence of major bleeding did not differ significantly between groups (6.5% vs 5.2%; P = 0.39), whereas minor bleeding was significantly more frequent in the aspirin group (14.9% vs 10.1%; P = 0.027).

Conclusions

Among patients undergoing low-to-intermediate risk noncardiac surgery >1 year after stent implantation primarily with a DES, in the setting of lower-than-expected event rates, we failed to identify a significant difference between perioperative aspirin monotherapy and no antiplatelet therapy with respect to ischemic outcomes or major bleeding. (Perioperative Antiplatelet Therapy in Patients With Drug-eluting Stent Undergoing Noncardiac Surgery [ASSURE-DES]; NCT02797548)
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阿司匹林单药治疗与不使用抗血小板疗法治疗接受中低风险非心脏手术的冠状动脉支架稳定期患者。
背景:目前的指南建议接受非心脏手术的冠状动脉药物洗脱支架(DES)患者围术期继续服用阿司匹林。然而,支持性证据有限:本研究旨在比较既往接受过 DES 植入术的患者在接受非心脏手术前继续使用阿司匹林单药治疗与暂时停止所有抗血小板治疗的差异:我们随机分配了接受 DES >1年且正在接受择期非心脏手术的患者,让他们在非心脏手术前5天继续服用阿司匹林或停用所有抗血小板药物。除非有禁忌症,否则建议在手术后 48 小时内恢复抗血小板治疗。主要结果是非心脏手术前5天至手术后30天内因任何原因死亡、心肌梗死、支架血栓或中风的综合结果:共有 1,010 名患者接受了随机分组。在改良意向治疗人群的926名患者中(阿司匹林单药治疗组462名患者,无抗血小板治疗组464名患者),阿司匹林单药治疗组有3名患者(0.6%)出现主要综合结果,无抗血小板治疗组有4名患者(0.9%)出现主要综合结果(差异,-0.2个百分点;95% CI:-1.3至0.9;P > 0.99)。两组均未出现支架血栓。两组大出血的发生率无显著差异(6.5% vs 5.2%;P = 0.39),而阿司匹林组轻微出血的发生率明显更高(14.9% vs 10.1%;P = 0.027):结论:在以DES为主的支架植入术后1年以上接受中低风险非心脏手术的患者中,在事件发生率低于预期的情况下,我们未能发现围手术期阿司匹林单药治疗与不进行抗血小板治疗在缺血性结果或大出血方面存在显著差异。(接受非心脏手术的药物洗脱支架患者围手术期抗血小板疗法[ASSURE-DES];NCT02797548)。
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来源期刊
CiteScore
42.70
自引率
3.30%
发文量
5097
审稿时长
2-4 weeks
期刊介绍: The Journal of the American College of Cardiology (JACC) publishes peer-reviewed articles highlighting all aspects of cardiovascular disease, including original clinical studies, experimental investigations with clear clinical relevance, state-of-the-art papers and viewpoints. Content Profile: -Original Investigations -JACC State-of-the-Art Reviews -JACC Review Topics of the Week -Guidelines & Clinical Documents -JACC Guideline Comparisons -JACC Scientific Expert Panels -Cardiovascular Medicine & Society -Editorial Comments (accompanying every Original Investigation) -Research Letters -Fellows-in-Training/Early Career Professional Pages -Editor’s Pages from the Editor-in-Chief or other invited thought leaders
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