Comparison of Different Chronic Maintenance Antithrombotic Strategies in Patients with Coronary Artery Disease: A Systematic Review and Network Meta-Analysis.

IF 3.4 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular Therapeutics Pub Date : 2023-08-17 eCollection Date: 2023-01-01 DOI:10.1155/2023/5446271
Junyan Zhang, Zhongxiu Chen, Yujia Cai, Chen Li, Yong He
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Abstract

Background: Optimal antithrombotic therapy during the chronic maintenance period in patients with coronary artery disease (CAD) is unknown. We compared five kinds of mainstream chronic maintenance antithrombotic strategies at least one year after the acute phase: aspirin alone, clopidogrel alone, ticagrelor alone, continued dual antiplatelet therapy (DAPT) for a period of time, and maintenance with aspirin combined with a low-dose anticoagulant such as rivaroxaban.

Methods: Ten randomized, controlled trials were selected using PubMed, Ovid MEDLINE, Embase, and Cochrane library through February 2023. The primary outcome was main adverse cardiac events (MACEs), and secondary outcomes include net adverse clinical events (NACEs), cardiac death, all-cause death, ischemic stroke, stent thrombosis, total bleeding, and major bleeding. A network meta-analysis was conducted with a random-effects model. Data extraction was performed by three independent reviewers.

Results: Our search identified ten eligible randomized controlled trials enrolling a total of 82,084 patients comparing different chronic maintenance antithrombotic strategies. As for the primary endpoint, there was no statistical difference in MACE outcomes between any two of the five methods. As for the secondary endpoint, there was no statistical difference in NACE, major bleeding, all-cause death, cardiac death, and stent thrombosis between any two methods. The aspirin plus low-dose rivaroxaban group had a lower incidence of ischemic stroke compared to the aspirin group (OR = 0.49, 95% CrI 0.26-0.91). And the prolonged DAPT group had a higher total bleeding rate compared to aspirin group (OR = 2.4, 95% CrI 1.1-5.9).

Conclusions: In terms of MACE, NACE, all-cause death, cardiac death, stent thrombosis, and major bleeding, there were no significant differences between using aspirin alone, clopidogrel alone, and ticagrelor alone; extending DAPT duration; and using aspirin combined with low-dose rivaroxaban for chronic maintenance antithrombotic regimens. However, choosing aspirin combined with low-dose rivaroxaban can reduce the incidence of ischemic stroke, and prolonged DAPT may have a higher rate of total bleeding. However, it is important to note that this study is based on indirect comparisons, and there is currently a lack of direct evidence comparing various maintenance antiplatelet therapy regimens. Further high-quality studies are needed to address this gap and provide more conclusive evidence on the comparative effectiveness of different maintenance antiplatelet strategies.

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冠心病患者不同慢性维持性抗血栓策略的比较:系统综述与网络元分析》。
背景:冠状动脉疾病(CAD)患者慢性维持期的最佳抗血栓治疗尚不清楚。我们比较了急性期后至少一年的五种主流慢性维持期抗血栓策略:单纯阿司匹林、单纯氯吡格雷、单纯替卡格雷、持续一段时间的双联抗血小板疗法(DAPT)以及阿司匹林联合低剂量抗凝剂(如利伐沙班)维持治疗:利用 PubMed、Ovid MEDLINE、Embase 和 Cochrane 图书馆,筛选出截至 2023 年 2 月的 10 项随机对照试验。主要结果为主要心脏不良事件(MACEs),次要结果包括净不良临床事件(NACEs)、心脏死亡、全因死亡、缺血性卒中、支架血栓、总出血和大出血。采用随机效应模型进行了网络荟萃分析。数据提取由三位独立审稿人完成:我们的搜索发现了十项符合条件的随机对照试验,共招募了 82,084 名患者,对不同的慢性维持性抗血栓策略进行了比较。在主要终点方面,五种方法中任何两种方法的MACE结果均无统计学差异。至于次要终点,任何两种方法在NACE、大出血、全因死亡、心源性死亡和支架血栓形成方面均无统计学差异。与阿司匹林组相比,阿司匹林加小剂量利伐沙班组的缺血性卒中发生率较低(OR = 0.49,95% CrI 0.26-0.91)。与阿司匹林组相比,延长DAPT组的总出血率更高(OR = 2.4,95% CrI 1.1-5.9):在MACE、NACE、全因死亡、心源性死亡、支架血栓和大出血方面,单独使用阿司匹林、单独使用氯吡格雷和单独使用替卡格雷、延长DAPT时间和使用阿司匹林联合小剂量利伐沙班作为慢性维持性抗栓方案之间没有显著差异。然而,选择阿司匹林联合小剂量利伐沙班可降低缺血性卒中的发生率,延长DAPT时间可能会有较高的总出血率。但需要注意的是,该研究是基于间接比较,目前缺乏直接证据比较各种维持性抗血小板治疗方案。需要进一步开展高质量的研究来弥补这一不足,并就不同的维持性抗血小板策略的比较效果提供更确凿的证据。
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来源期刊
Cardiovascular Therapeutics
Cardiovascular Therapeutics 医学-心血管系统
CiteScore
5.60
自引率
0.00%
发文量
55
审稿时长
6 months
期刊介绍: Cardiovascular Therapeutics (formerly Cardiovascular Drug Reviews) is a peer-reviewed, Open Access journal that publishes original research and review articles focusing on cardiovascular and clinical pharmacology, as well as clinical trials of new cardiovascular therapies. Articles on translational research, pharmacogenomics and personalized medicine, device, gene and cell therapies, and pharmacoepidemiology are also encouraged. Subject areas include (but are by no means limited to): Acute coronary syndrome Arrhythmias Atherosclerosis Basic cardiac electrophysiology Cardiac catheterization Cardiac remodeling Coagulation and thrombosis Diabetic cardiovascular disease Heart failure (systolic HF, HFrEF, diastolic HF, HFpEF) Hyperlipidemia Hypertension Ischemic heart disease Vascular biology Ventricular assist devices Molecular cardio-biology Myocardial regeneration Lipoprotein metabolism Radial artery access Percutaneous coronary intervention Transcatheter aortic and mitral valve replacement.
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