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口服直接凝血酶抑制剂希美加群用于近期心肌损伤患者(ESTEEM试验)的疗效和安全性:希美加群对急性心肌梗死后房颤患者缺血事件及死亡的影响

Effect of ximelagatran on ischemic events and death in patients with atrial fibrillation after acute myocardial infarction in the efficacy and safety of the oral direct thrombin inhibitor ximelagatran in patients with recent myocardial damage (ESTEEM) trial.

作者信息

Tangelder Marco J D, Frison Lars, Weaver Douglas, Wilcox Robbert G, Bylock Anders, Emanuelsson Håkan, Held Peter, Oldgren Jonas

机构信息

AstraZeneca R&D, Medical Science, Mölndal, Sweden.

出版信息

Am Heart J. 2008 Feb;155(2):382-7. doi: 10.1016/j.ahj.2007.08.035.

Abstract

BACKGROUND

New-onset trial fibrillation (AF) occurs commonly after acute myocardial infarction (MI) and is associated with a poor prognosis due to stroke or death. The optimal antithrombotic therapy is unknown. The aim of this study was to investigate whether an oral direct thrombin inhibitor, ximelagatran, added to aspirin, reduced the risk of death, myocardial infarction (MI), and stroke in patients who developed AF after their qualifying MI in the efficacy and safety of the oral direct thrombin inhibitor ximelagatran in patients with recent myocardial damage (ESTEEM) trial.

METHODS

The ESTEEM trial evaluated 6 months treatment with ximelagatran together with aspirin, compared to aspirin alone, for prevention of ischemic events in 1883 patients randomized within 14 days after an MI. After their qualifying MI, 174 (9%) patients developed AF in hospital. Multivariate hazard ratios for ximelagatran compared with placebo were calculated by presence AF.

RESULTS

Of 101 patients with AF treated with ximelagatran 7 (6.9%) had either death, MI, or stroke, compared with 15 (20.6%) in 73 patients allocated to placebo. Ximelagatran reduced the risk of death, MI, or stroke by 70% (hazard ratio 0.30, 95% CI 0.12-0.74). For the separate outcome events, we found similar, nonsignificant trends. One major bleeding event occurred in each treatment group.

CONCLUSIONS

For patients with MI complicated by AF, the combination of aspirin and an oral direct thrombin inhibitor seems beneficial. The high risk for death, MI, and stroke in this population and the increasing use of percutaneous interventions in MI patients may suggest a combination of long-term antiplatelet and anticoagulant therapy. Randomized clinical trials are warranted.

摘要

背景

新发房颤(AF)常见于急性心肌梗死(MI)后,因中风或死亡而预后不良。最佳抗栓治疗方案尚不清楚。本研究旨在探讨在近期心肌损伤患者口服直接凝血酶抑制剂希美加群有效性和安全性试验(ESTEEM试验)中,在阿司匹林基础上加用口服直接凝血酶抑制剂希美加群是否能降低心肌梗死合格患者发生AF后死亡、心肌梗死(MI)和中风的风险。

方法

ESTEEM试验评估了希美加群联合阿司匹林治疗6个月与单用阿司匹林相比,对1883例在MI后14天内随机分组患者预防缺血事件的效果。在其合格的MI后,174例(9%)患者在住院期间发生AF。根据是否存在AF计算希美加群与安慰剂相比的多变量风险比。

结果

在101例接受希美加群治疗的AF患者中,7例(6.9%)发生死亡、MI或中风,而在73例接受安慰剂治疗的患者中,有15例(20.6%)发生。希美加群使死亡、MI或中风风险降低70%(风险比0.30,95%CI 0.12 - 0.74)。对于单独的结局事件,我们发现了类似的、无显著意义的趋势。每个治疗组均发生1例严重出血事件。

结论

对于MI合并AF的患者,阿司匹林与口服直接凝血酶抑制剂联合使用似乎有益。该人群死亡、MI和中风风险高,且MI患者经皮介入治疗使用增加,可能提示长期抗血小板和抗凝治疗联合使用。有必要进行随机临床试验。

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