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动脉瘤性蛛网膜下腔出血的抗纤溶治疗

Antifibrinolytic therapy for aneurysmal subarachnoid haemorrhage.

作者信息

Roos Y B W E M, Rinkel G J E, Vermeulen M, Algra A, van Gijn J

机构信息

Dept. of Neurology, Academic Medical Center, Meibergdreef 9, Amsterdam, Netherlands.

出版信息

Cochrane Database Syst Rev. 2003(2):CD001245. doi: 10.1002/14651858.CD001245.

Abstract

BACKGROUND

Rebleeding is an important cause of death and disability in people with aneurysmal subarachnoid haemorrhage. Rebleeding is probably due to dissolution of the clot by natural fibrinolytic activity.

OBJECTIVES

The objective of this review was to assess the effect of antifibrinolytic treatment in patients with aneurysmal subarachnoid haemorrhage.

SEARCH STRATEGY

We searched the Cochrane Stroke Group Trials Register, the Cochrane Controlled Trials Register, Medline and Embase (last searched June 2002) and reference lists of articles. We also contacted drug companies.

SELECTION CRITERIA

Randomised trials comparing oral or intravenous antifibrinolytic drugs (tranexamic acid, epsilon amino-caproic acid or an equivalent) with control in people with confirmed subarachnoid haemorrhage.

DATA COLLECTION AND ANALYSIS

Two reviewers independently selected trials for inclusion and extracted the data. All five reviewers assessed trial quality.

MAIN RESULTS

Nine trials involving 1399 patients were included. Based on 1041 patients in three trials, antifibrinolytic treatment did not show any evidence of benefit for poor outcome (death, vegetative state or severe disability) with an odds ratio of 1.12, 95% confidence interval 0.88 to 1.43. Death from all causes was not significantly influenced by treatment across all nine trials (odds ratio 0.99, 95% confidence interval 0.79 to 1.24). Antifibrinolytic treatment reduced the risk of re-bleeding reported at the end of follow-up, with some heterogeneity between the trials (odds ratio 0.55, 95% confidence interval 0.42 to 0.71). Treatment increased the risk of cerebral ischaemia in five trials (odds ratio 1.39, 95% confidence interval 1.07 to 1.82) with considerable heterogeneity between the most recent study (Roos 2000), in which specific treatments to prevent cerebral ischemia were used, and the four older studies. Antifibrinolytic treatment showed no effect on the reported rate of hydrocephalus in five trials (odds ratio 1.14, 95% confidence interval 0.86 to 1.51).

REVIEWER'S CONCLUSIONS: Treatment does not improve clinical outcome because the benefit is offset by an increase in poor outcome caused by cerebral ischemia as a result of treatment with antifibrinolytics. These data do not support the routine use of antifibrinolytic drugs in the treatment of patients with aneurysmal subarachnoid haemorrhage.

摘要

背景

再出血是动脉瘤性蛛网膜下腔出血患者死亡和致残的重要原因。再出血可能是由于天然纤溶活性溶解血凝块所致。

目的

本综述的目的是评估抗纤溶治疗对动脉瘤性蛛网膜下腔出血患者的疗效。

检索策略

我们检索了Cochrane卒中组试验注册库、Cochrane对照试验注册库、Medline和Embase(最后检索时间为2002年6月)以及文章的参考文献列表。我们还联系了制药公司。

入选标准

比较口服或静脉注射抗纤溶药物(氨甲环酸、ε-氨基己酸或等效药物)与确诊蛛网膜下腔出血患者对照组的随机试验。

数据收集与分析

两名评价者独立选择纳入试验并提取数据。所有五名评价者评估试验质量。

主要结果

纳入了9项涉及1399例患者的试验。基于三项试验中的1041例患者,抗纤溶治疗未显示出对不良结局(死亡、植物状态或严重残疾)有任何益处,优势比为1.12,95%置信区间为0.88至1.43。在所有九项试验中,治疗对各种原因导致的死亡没有显著影响(优势比0.99,95%置信区间0.79至1.24)。抗纤溶治疗降低了随访结束时报告的再出血风险,试验之间存在一些异质性(优势比0.55,95%置信区间0.42至0.71)。在五项试验中,治疗增加了脑缺血风险(优势比1.39,95%置信区间1.07至1.82),在最近的研究(Roos 2000)中使用了预防脑缺血的特定治疗方法,与四项较早的研究之间存在相当大的异质性。在五项试验中,抗纤溶治疗对报告的脑积水发生率没有影响(优势比1.14,95%置信区间0.86至1.51)。

综述作者结论

治疗并不能改善临床结局,因为抗纤溶治疗导致的脑缺血增加了不良结局,抵消了其益处。这些数据不支持在动脉瘤性蛛网膜下腔出血患者治疗中常规使用抗纤溶药物。

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