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现状:经皮冠状动脉介入治疗和冠状动脉支架植入术后双联抗血小板治疗的持续时间——过去、现在和未来的观点。

State of the art: duration of dual antiplatelet therapy after percutaneous coronary intervention and coronary stent implantation - past, present and future perspectives.

机构信息

Department of Cardiology, Bern University Hospital, University of Bern, Bern, Switzerland.

出版信息

EuroIntervention. 2017 Aug 25;13(6):717-733. doi: 10.4244/EIJ-D-17-00468.

Abstract

Evidence from studies published more than 10 years ago suggested that patients receiving first-generation drug-eluting stents (DES) needed dual antiplatelet therapy (DAPT) for at least 12 months. Current evidence from randomised controlled trials (RCT) reported within the past five years suggests that patients with stable ischaemic heart disease who receive newer-generation DES need DAPT for a minimum of three to six months. Patients who undergo stenting for an acute coronary syndrome benefit from DAPT for at least 12 months, but a Bayesian network meta-analysis confirms that extending DAPT beyond 12 months confers a trade-off between reduced ischaemic events and increased bleeding. However, the network meta-analysis finds no credible increase in all-cause mortality if DAPT is lengthened from three to six months to 12 months (posterior median odds ratio [OR] 0.98; 95% Bayesian credible interval [BCI]: 0.73-1.43), from 12 months to 18-48 months (OR 0.87; 95% BCI: 0.64-1.17), or from three to six months to 18-48 months (OR 0.86; 95% BCI: 0.63-1.21). Future investigation should focus on identifying scoring systems that have excellent discrimination and calibration. Although predictive models should be incorporated into systems of care, most decisions about DAPT duration will be based on clinical judgement and patient preference.

摘要

来自 10 多年前发表的研究的证据表明,接受第一代药物洗脱支架 (DES) 的患者需要进行至少 12 个月的双联抗血小板治疗 (DAPT)。最近五年内随机对照试验 (RCT) 的证据表明,接受新一代 DES 的稳定型缺血性心脏病患者需要进行至少 3 至 6 个月的 DAPT。因急性冠脉综合征接受支架置入术的患者需要进行至少 12 个月的 DAPT,但贝叶斯网络荟萃分析证实,延长 DAPT 时间超过 12 个月,在减少缺血事件和增加出血之间存在权衡。然而,该网络荟萃分析发现,将 DAPT 从 3 个月延长至 6 个月至 12 个月(后验中位数比值比 [OR] 0.98;95%贝叶斯可信区间 [BCI]:0.73-1.43)、从 12 个月延长至 18-48 个月(OR 0.87;95% BCI:0.64-1.17)或从 3 个月至 6 个月至 18-48 个月(OR 0.86;95% BCI:0.63-1.21)并不会导致全因死亡率的可信增加。未来的研究应重点关注识别具有良好区分度和校准度的评分系统。尽管预测模型应纳入护理系统,但 DAPT 持续时间的大多数决策将基于临床判断和患者偏好。

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