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急性缺血性卒中后3至4.5小时组织型纤溶酶原激活剂的疗效与安全性:一项荟萃分析。

Efficacy and safety of tissue plasminogen activator 3 to 4.5 hours after acute ischemic stroke: a metaanalysis.

作者信息

Lansberg Maarten G, Bluhmki Erich, Thijs Vincent N

机构信息

Stanford Stroke Center, Stanford University Medical Center, Palo Alto, CA 94304-9705, USA.

出版信息

Stroke. 2009 Jul;40(7):2438-41. doi: 10.1161/STROKEAHA.109.552547. Epub 2009 May 28.

Abstract

BACKGROUND AND PURPOSE

The Third European Cooperative Acute Stroke Study (ECASS-3) demonstrated a benefit of treatment with intravenous tissue plasminogen activator (tPA) for acute stroke in the 3- to 4.5-hour time-window. Prior studies, however, have failed to demonstrate a significant benefit of tPA for patients treated beyond 3 hours. The purpose of this study was to produce reliable and precise estimates of the treatment effect of tPA by pooling data from all relevant studies.

METHODS

A metaanalysis was undertaken to determine the efficacy of tPA in the 3- to 4.5-hour time-window. The effect of tPA on favorable outcome and mortality was assessed.

RESULTS

The metaanalysis included data from patients treated in the 3- to 4.5-hour time-window in ECASS-1 (n=234), ECASS-2 (n=265), ECASS-3 (n=821) and The Alteplase Thrombolysis for Acute Noninterventional Therapy in Ischemic Stroke (ATLANTIS) (n=302). tPA treatment was associated with an increased chance of favorable outcome (odds ratio 1.31; 95% CI: 1.10 to 1.56; P=0.002) and no significant difference in mortality (odds ratio 1.04; 95% CI: 0.75 to 1.43; P=0.83) compared to placebo treated patients.

CONCLUSIONS

Treatment with tPA in the 3- to 4.5-hour time-window is beneficial. It results in an increased rate of favorable outcome without adversely affecting mortality.

摘要

背景与目的

第三次欧洲急性卒中协作研究(ECASS - 3)表明,在3至4.5小时时间窗内,静脉注射组织型纤溶酶原激活剂(tPA)治疗急性卒中具有益处。然而,先前的研究未能证明tPA对超过3小时治疗的患者有显著益处。本研究的目的是通过汇总所有相关研究的数据,对tPA的治疗效果做出可靠且精确的估计。

方法

进行一项荟萃分析以确定tPA在3至4.5小时时间窗内的疗效。评估tPA对良好预后和死亡率的影响。

结果

荟萃分析纳入了来自ECASS - 1(n = 234)、ECASS - 2(n = 265)、ECASS - 3(n = 821)和急性缺血性卒中阿替普酶溶栓非介入治疗(ATLANTIS)(n = 302)中在3至4.5小时时间窗内接受治疗患者的数据。与接受安慰剂治疗的患者相比,tPA治疗与良好预后几率增加相关(优势比1.31;95%可信区间:1.10至1.56;P = 0.002),且死亡率无显著差异(优势比1.04;95%可信区间:0.75至1.43;P = 0.83)。

结论

在3至4.5小时时间窗内使用tPA治疗有益。它能提高良好预后率,且不影响死亡率。

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