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经皮冠状动脉介入治疗的冠心病患者的个体化抗血小板治疗:随机临床试验的网络荟萃分析。

Personalized antiplatelet therapy in patients with coronary artery disease undergoing percutaneous coronary intervention: A network meta-analysis of randomized clinical trials.

机构信息

Department of Internal Medicine, Hurley Medical Center/Michigan State University, Flint, Michigan.

Division of Hematology & Oncology, St. John Hospital, Grosse Pointe Woods, Michigan.

出版信息

Catheter Cardiovasc Interv. 2019 Aug 1;94(2):181-186. doi: 10.1002/ccd.28075. Epub 2019 Jan 10.

DOI:10.1002/ccd.28075
PMID:30628754
Abstract

OBJECTIVES

This study aimed to evaluate the efficacy and safety of genotype- and phenotype-guided intensified antiplatelet therapy compared with conventional therapy in patients undergoing stent implantation.

BACKGROUND

Although potent P2Y receptor inhibitors are recommended for percutaneous coronary intervention (PCI)-treated acute coronary syndrome, their usage is limited by a high bleeding risk. Therefore, personalized antiplatelet therapy could provide a valuable foundation for selection of antiplatelet therapy in this population.

METHODS

We conducted a Bayesian network meta-analysis for all randomized clinical trials (RCTs) that evaluated genotype- and/or phenotype-guided therapy in PCI-treated coronary artery disease.

RESULTS

Thirteen RCTs were included with a total of 6,845 patients. The results showed no significant differences in major adverse cardiovascular events (MACE) between the treatment options ((genotype guided vs. standard of care; OR 0.64; 95% CI: 0.38-1.05) and (phenotype vs. standard of care; OR 0.93; 95% CI: 0.54-1.37)). In addition, no significant differences were demonstrated in bleeding events ((genotype guided vs. standard of care; OR 0.73; 95% CI: 0.45-1.25) and (phenotype vs. standard of care; OR 0.90; 95% CI: 0.62-1.39)).

CONCLUSIONS

In this mixed treatment meta-analysis of RCTs, neither genotype- nor phenotype-guided antiplatelet therapy in patients with PCI-treated coronary artery disease was superior to conventional therapy.

摘要

目的

本研究旨在评估与传统治疗相比,基因分型和表型指导的强化抗血小板治疗在接受支架植入术的患者中的疗效和安全性。

背景

尽管对于经皮冠状动脉介入治疗(PCI)治疗的急性冠状动脉综合征强烈推荐使用强效 P2Y 受体抑制剂,但由于出血风险较高,其使用受到限制。因此,个性化抗血小板治疗可能为该人群的抗血小板治疗选择提供有价值的基础。

方法

我们对所有评估 PCI 治疗的冠心病患者进行了基因分型和/或表型指导治疗的随机临床试验(RCT)的贝叶斯网络荟萃分析。

结果

纳入了 13 项 RCT,共 6845 例患者。结果显示,治疗方案之间在主要不良心血管事件(MACE)方面没有显著差异((基因分型指导与标准治疗相比;OR 0.64;95%CI:0.38-1.05)和(表型与标准治疗相比;OR 0.93;95%CI:0.54-1.37))。此外,在出血事件方面也未显示出显著差异((基因分型指导与标准治疗相比;OR 0.73;95%CI:0.45-1.25)和(表型与标准治疗相比;OR 0.90;95%CI:0.62-1.39))。

结论

在这项对 RCT 的混合治疗荟萃分析中,在接受 PCI 治疗的冠心病患者中,基因分型或表型指导的抗血小板治疗均不比常规治疗更具优势。

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