Comparative outcomes of clopidogrel vs aspirin monotherapy in post- pci patients: An updated systematic review and meta-analysis.

IF 1.6 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Shariq Ahmad Wani, Muhammad Abdullah Naveed, Bazil Azeem, Saad Ashraf, Ahila Ali, Talha Ali, Faiza Fatima, Momin Shah, M D Sivaram Neppala, Raheel Ahmed
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引用次数: 0

Abstract

Current guidelines recommend 6-12 months of dual antiplatelet therapy (DAPT) after percutaneous coronary intervention(PCI) followed by aspirinin monotherapy indefinitely. We aimed to assess efficacy and safety of Clopidogrel as compared to aspirin in patients undrgoing PCI after completing DAPT. We systematically searched 3 electronic databases and identified studies comparing clopidogrel to aspirin in post PCI population after completing DAPT. We included 7 studies with 20,360 patients. We pooled outcomes for major adverse cardiac events (MACE), typically comprising a composite of death, myocardial infarction (MI), or stroke; all-cause mortality; cardiac death; major bleeding; any stroke; ischemic stroke; hemorrhagic stroke; repeat revascularization; target-vessel revascularization (TVR); and definite stent thrombosis. Mean follow up was 12-36 months. Duration of DAPT was 1-18 months. Clopidogrel was associated with reductions in MACE than aspirin (RR: 0.82; 95 % CI: 0.69-0.98; p = 0.03), showed reduced risk of MI (RR 0.93 CI 0.60-1.44; p 0.74, I2 63%) indicating a relative reduction of 7 %, reduced strokes numerically but non-significantly (RR: 0.72; 95 % CI: 0.48-1.07; p = 0.11), RRR 28 %, all cause mortality did not exhibit a significant difference between clopidogrel and aspirin (RR: 0.99; 95 % CI: 0.67-1.44; p = 0.94). Cardiac death (RR: 0.81; 95 % CI: 0.56-1.17; p = 0.26), major bleeding (RR: 0.90; 95 % CI: 0.61-1.33; p = 0.61), reflecting a 10 % non-significant relative reduction, repeat revascularization showed no significant difference (RR: 0.95; 95 % CI: 0.74-1.23; p = 0.72) representing a slight 5 % relative reduction, target vessel revascularization did not reveal any significant differences (RR: 0.89; 95 % CI: 0.69-1.16; p = 0.40) corresponding to a non-significant relative risk reduction of 11 %, stent thrombosis demonstrated no statistically significant difference (RR: 0.78; 95 % CI: 0.27-2.31; p = 0.66) RRR of 22 %. Compared to aspirin Clopidogrel was associated with reduction in MACE with no significant differences in Mortality, Major bleeding, MI, and repeat revascularization between groups. PROSPERO REGISTRATION NUMBER: CRD420251042349.

氯吡格雷与阿司匹林单药治疗pci后患者的比较结果:最新的系统回顾和荟萃分析。
目前的指南建议在经皮冠状动脉介入治疗(PCI)后进行6-12个月的双重抗血小板治疗(DAPT),然后无限期地进行阿斯匹林单药治疗。我们的目的是评估氯吡格雷与阿司匹林在完成DAPT后接受PCI的患者中的疗效和安全性。我们系统地检索了3个电子数据库,并确定了比较氯吡格雷和阿司匹林在完成DAPT后PCI患者中的研究。我们纳入了7项研究,共20360例患者。我们汇总了主要心脏不良事件(MACE)的结局,通常包括死亡、心肌梗死(MI)或中风;全因死亡率;心脏死亡;主要出血;任何中风;缺血性中风;出血性中风;重复血管再生;靶血管重建术;明确的支架血栓形成。平均随访12-36个月。DAPT疗程1 ~ 18个月。氯吡格雷比阿司匹林与MACE降低相关(RR: 0.82;95% ci: 0.69-0.98;p = 0.03),显示心肌梗死风险降低(RR 0.93 CI 0.60-1.44;p 0.74, I2 63%)表明相对减少了7%,减少了中风数量,但无显著性(RR: 0.72;95% ci: 0.48-1.07;p = 0.11), RRR为28%,氯吡格雷与阿司匹林的全因死亡率无显著差异(RR: 0.99;95% ci: 0.67-1.44;p = 0.94)。心源性死亡(RR: 0.81;95% ci: 0.56-1.17;p = 0.26),大出血(RR: 0.90;95% ci: 0.61-1.33;p = 0.61),反映了10%的非显著性相对减少,重复血运重建术无显著性差异(RR: 0.95;95% ci: 0.74-1.23;p = 0.72),相对减少5%,靶血管重建术未显示任何显著差异(RR: 0.89;95% ci: 0.69-1.16;p = 0.40),相对危险度降低11%,支架内血栓形成差异无统计学意义(RR: 0.78;95% ci: 0.27-2.31;p = 0.66),风险比为22%。与阿司匹林相比,氯吡格雷与MACE降低相关,两组间死亡率、大出血、心肌梗死和重复血运重建术无显著差异。普洛斯彼罗注册号:crd420251042349。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cardiovascular Revascularization Medicine
Cardiovascular Revascularization Medicine CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
3.30
自引率
5.90%
发文量
687
审稿时长
36 days
期刊介绍: Cardiovascular Revascularization Medicine (CRM) is an international and multidisciplinary journal that publishes original laboratory and clinical investigations related to revascularization therapies in cardiovascular medicine. Cardiovascular Revascularization Medicine publishes articles related to preclinical work and molecular interventions, including angiogenesis, cell therapy, pharmacological interventions, restenosis management, and prevention, including experiments conducted in human subjects, in laboratory animals, and in vitro. Specific areas of interest include percutaneous angioplasty in coronary and peripheral arteries, intervention in structural heart disease, cardiovascular surgery, etc.
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