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《2007年急性卒中的阿替普酶治疗:我们可采用的一种有效治疗选择》

[Alteplase treatment for acute stroke 2007: an effective therapeutic option at our disposal].

作者信息

Carneado-Ruiz J, Saver J L

机构信息

Unidad de Ictus, Servicio de Neurología, Hospital General Universitario de Alicante, 03010, Alicante, Spain.

出版信息

Rev Neurol. 2007;45(1):42-52.

PMID:17620265
Abstract

INTRODUCTION

The greatest progress has been made in the research field based on the early arterial recanalization strategy in cerebral ischemia.

AIM

To carry out a revision of stroke treatment with intravenous thrombolysis during the therapeutic window period covering the first three hours of evolution. The revision focuses on information provided by clinical trials, meta-analysis and open-label reports studies.

DEVELOPMENT

Clinical trials that study the use of alteplase in the acute stroke treatment, especially the two phase III clinical trials carried out by the National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group, are described. A great deal of useful information has been provided through systematic revisions that analyze data on these treatment clinical trials jointly. Meta-analysis studies are described: the Pooled Analysis of ATLANTIS, ECASS and NINDS t-PA Stroke Trials, Cochrane Meta-analysis: Thrombolysis for Acute Ischemic Stroke. Community based studies, especially the SITS-MOST study, were revised, and their findings were compared with other open-label t-PA studies.

CONCLUSIONS

t-PA is effective when administered in the first three hours of evolution of stroke in selected patients and under ideal conditions, and it may be beneficial, using the same selection criteria, in a therapeutic window of four and a half hours. The treatment is effective when applied as part of the daily clinical practice in our environment. This effectiveness does not disappear when extending its use to a large number of qualified hospitals.

摘要

引言

基于脑缺血早期动脉再通策略的研究领域取得了最大进展。

目的

对治疗窗为发病后前三小时的静脉溶栓治疗中风进行综述。该综述聚焦于临床试验、荟萃分析和开放标签报告研究提供的信息。

进展

描述了研究阿替普酶在急性中风治疗中应用的临床试验,尤其是美国国立神经疾病和中风研究所rt-PA中风研究组开展的两项III期临床试验。通过联合分析这些治疗临床试验数据的系统综述提供了大量有用信息。描述了荟萃分析研究:阿替普酶治疗急性缺血性中风的汇总分析、Cochrane荟萃分析:急性缺血性中风溶栓治疗。对基于社区的研究,尤其是SITS-MOST研究进行了综述,并将其结果与其他开放标签的阿替普酶研究进行了比较。

结论

在选定患者且处于理想条件下,阿替普酶在中风发病后前三小时给药有效,并且在相同选择标准下,在4.5小时的治疗窗内可能有益。在我们的环境中,作为日常临床实践的一部分应用该治疗是有效的。当将其应用扩展到大量合格医院时,这种有效性不会消失。

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Rev Neurol. 2007;45(1):42-52.
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