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台湾地区急性心肌梗死患者新接受替格瑞洛与氯吡格雷治疗的心血管和出血风险。

Cardiovascular and Bleeding Risks in Acute Myocardial Infarction Newly Treated With Ticagrelor vs. Clopidogrel in Taiwan.

机构信息

Department of Internal Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University.

Department of Pharmacy, Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University.

出版信息

Circ J. 2018 Feb 23;82(3):747-756. doi: 10.1253/circj.CJ-17-0632. Epub 2017 Oct 27.

Abstract

BACKGROUND

There are few data on ticagrelor in Asian patients. This study evaluated clinical outcomes with ticagrelor and clopidogrel in Taiwanese patients with acute myocardial infarction (AMI).Methods and Results:We used the Taiwan National Health Insurance Research Database to identify 27,339 AMI patients aged ≥18 years between January 2012 and December 2014, and only patients who survived greater than or equal to 30 days after AMI and took dual antiplatelet therapy were included. Cohorts of ticagrelor and clopidogrel were matched 1:8, based on propensity score matching, to balance baseline covariates. The primary efficacy endpoints were death from any cause, AMI, or stroke. The safety endpoints consisted of major gastrointestinal bleeding or intracerebral hemorrhage. Following propensity matching, the primary efficacy endpoint rate was 22% lower in the ticagrelor group than in the clopidogrel group (10.6% and 16.2%, respectively; adjusted HR, 0.779; 95% CI: 0.684-0.887). The safety endpoint rate was similar between the ticagrelor and clopidogrel groups (3.2% and 4.1% respectively; adjusted HR, 0.731; 95% CI: 0.522-1.026).

CONCLUSIONS

In real-world AMI Taiwanese patients, ticagrelor seemed to offer better anti-ischemic protection than clopidogrel, without an increase in the rate of major bleeding. A large-scale randomized trial is needed to assess the efficacy and safety of ticagrelor in East Asian AMI patients.

摘要

背景

亚洲患者使用替格瑞洛的数据较少。本研究评估了替格瑞洛和氯吡格雷在台湾急性心肌梗死(AMI)患者中的临床结局。

方法和结果

我们使用台湾全民健康保险研究数据库,确定了 2012 年 1 月至 2014 年 12 月期间年龄≥18 岁的 27339 例 AMI 患者,仅纳入 AMI 后存活时间≥30 天并接受双联抗血小板治疗的患者。根据倾向评分匹配,将替格瑞洛组和氯吡格雷组按 1:8 进行匹配,以平衡基线协变量。主要疗效终点为任何原因导致的死亡、AMI 或卒中等复合终点。安全性终点包括主要胃肠道出血或颅内出血。经倾向评分匹配后,替格瑞洛组的主要疗效终点发生率比氯吡格雷组低 22%(分别为 10.6%和 16.2%;调整后的 HR:0.779;95%CI:0.684-0.887)。替格瑞洛组和氯吡格雷组的安全性终点发生率相似(分别为 3.2%和 4.1%;调整后的 HR:0.731;95%CI:0.522-1.026)。

结论

在真实世界的台湾 AMI 患者中,替格瑞洛似乎比氯吡格雷提供了更好的抗缺血保护作用,且不会增加大出血的发生率。需要开展大规模随机试验,评估替格瑞洛在东亚 AMI 患者中的疗效和安全性。

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