首页> 外文期刊>Journal of cardiovascular pharmacology and therapeutics >De-Escalation of Antiplatelet Therapy in Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention: A Meta-Analysis of Randomized Clinical Trials
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De-Escalation of Antiplatelet Therapy in Patients With Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention: A Meta-Analysis of Randomized Clinical Trials

机译:急性冠状动脉综合征患者经皮冠状动脉介入的患者抗血小板治疗脱升升级:随机临床试验的荟萃分析

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Aims: Patients with acute coronary syndrome undergoing percutaneous coronary intervention (PCI) are recommended to be placed on potent P2Y12 blockade. However, the long-term bleeding risk is high. Therefore, despite no definitive evidence, switching to clopidogrel beyond the acute phase is common. We aimed to evaluate the clinical outcomes of antiplatelet de-escalation compared with continuation in patients treated with PCI. Methods: We searched databases for randomized clinical trials (RCTs) that evaluated the safety and efficacy of antiplatelet de-escalation compared with continuation in patients treated with PCI. Pooled summary estimates were calculated. Results: We included 3 RCTs with 3391 patients (median follow-up: 12 months). Compared with the continued group, the net clinical outcome (composite of bleeding or thrombotic events) was significantly reduced in the group switched to clopidogrel (8.7% vs 12.1%; risk ratio [RR]: 0.64; 95% confidence interval [CI]: 0.43-0.97; P = .03). However, there were similar clinical outcomes between groups for major adverse cardiovascular events (MACE; RR: 0.78; 95% CI: 0.55-1.11; P = .17), all Bleeding Academic Research Consortium (BARC) types bleeding (RR: 0.61; 95% CI: 0.33-1.11; P = .10), or BARC types >= 2 bleeding (RR: 0.49; 95% CI: 0.19-1.26; P = .14). Conclusions: Our results suggest a net clinical benefit of de-escalation therapy shortly after PCI, without increased risk of MACE. Larger randomized trials will be necessary to confirm these findings.
机译:目的:建议经皮冠状动脉综合征(PCI)进行经皮冠状动脉综合征(PCI)的患者放在有效的P2Y12封闭上。然而,长期出血风险很高。因此,尽管没有明确的证据,但转向氯吡格雷超出急性期是常见的。我们的旨在评估抗血小板脱升升级的临床结果与用PCI治疗的患者的延续相比。方法:我们搜索了随机临床试验(RCT)的数据库,其评估了抗血小板脱升升级的安全性和功效与PCI治疗的患者的延续相比。计算汇总摘要估计。结果:我们包括3名RCT,3391名患者(中位随访:12个月)。与持续的组相比,转向氯吡格雷的组中的净临床结果(出血或血栓形成的复合事件)显着降低了(8.7%Vs 12.1%;风险比[RR]:0.64; 95%置信区间[CI]: 0.43-0.97; p = .03)。然而,对于主要不良心血管事件(MACE; RR:0.78; 95%CI:0.55-1.11; P = .17),所有出血学术研究联盟(BARC)类型出血(RR:0.61; 95%CI:0.33-1.11; p = .10),或Barc类型> = 2出血(RR:0.49; 95%CI:0.19-1.26; P = .14)。结论:我们的结果表明PCI后不久脱升升级治疗的净临床效益,而不会增加迈斯风险。较大的随机试验将是确认这些发现的必要条件。

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