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银杏叶提取物在急性缺血性卒中中的应用。

The use of Ginkgo biloba extract in acute ischemic stroke.

作者信息

Liu Jianping

机构信息

Beijing University of Chinese Medicine's Evidence-based Chinese Medicine Center for Clinical Research and Evaluation.

出版信息

Explore (NY). 2006 May;2(3):262-3. doi: 10.1016/j.explore.2006.03.012.

Abstract

BACKGROUND

Ginkgo biloba extract is widely used in the treatment of acute ischemic stroke in China. The Cochrane Re-view authors aimed to assess the evidence from randomized controlled trials and quasirandomized controlled trials on the use of Ginkgo biloba extract in acute ischemic stroke.

OBJECTIVES

The primary objective is to determine whether Ginkgo biloba extract improves functional outcome without causing undue harm in patients with acute ischemic stroke. Secondary objectives are to assess the effect of Ginkgo biloba extract on neurological impairment and quality of life.

SEARCH STRATEGY

The authors searched the Cochrane Stroke Group Trials Register (last searched October 2004), the Trials Register of the Cochrane Complementary Medicine Field (last searched October 2004), and the Chinese Stroke Trials Register (last searched June 2004). In addition,the authors searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 3,2004), MEDLINE (1966 to August 2004), EMBASE (1980 to June 2004), AMED(1985 to May 2002), and the China Biological Medicine Database (CBM-disk,1979 to August 2004). The authors searched relevant clinical trials and re-search registers and contacted pharmaceutical companies and researchers in an ef-fort to identify further published and unpublished studies.

SELECTION CRITERIA

Randomized controlled trials or quasirandomized controlled clinical trials comparing Ginkgo biloba extract with placebo or open control(no placebo) in patients with acute ischemic stroke.

DATA COLLECTION AND ANALYSIS

Two authors independently selected trials for inclusion, assessed trial quality, and extracted data.

MAIN RESULTS

Fourteen trials were identified, of which 10 trials (792 patients)were included. Four trials are awaiting assessment. In the 10 included trials, follow-up was performed at 14 to 35 days after stroke. In all studies, neurological outcome was assessed, but none of them reported on disability (activities of daily living function) or quality of life. Only three trials reported adverse events. In nine trials, all of them assessed to be of inferior quality, significant improvement in neurological deficit at the end of the treatment was used as the outcome measure. When analyzing these trials together, Ginkgo biloba extract was associated with a significant increase in the number of improved patients (Peto odds ratio (OR)2.66; 95% confidence interval (CI): 1.79-3.94). One placebo-controlled trial, assessed to be of good quality, reported neurological outcome as a continuous variable. It failed to show an improvement of neurological deficit at the end of treatment (weighted mean difference (fixed)0.81; 95% CI: -8.9-10.52). No deaths or major adverse events were reported during the follow-up period.

CONCLUSIONS

There was no convincing evidence from trials of sufficient methodological quality to support the routine use of Ginkgo biloba extract to promote recovery after stroke. High-quality and large-scale randomized controlled trials are needed to test its efficacy.

摘要

背景

在中国,银杏叶提取物被广泛用于治疗急性缺血性中风。Cochrane系统评价的作者旨在评估随机对照试验和半随机对照试验中关于银杏叶提取物用于急性缺血性中风的证据。

目的

主要目的是确定银杏叶提取物是否能改善急性缺血性中风患者的功能结局且不造成不当伤害。次要目的是评估银杏叶提取物对神经功能缺损和生活质量的影响。

检索策略

作者检索了Cochrane中风组试验注册库(最后检索时间为2004年10月)、Cochrane补充医学领域试验注册库(最后检索时间为2004年10月)以及中国中风试验注册库(最后检索时间为2004年6月)。此外,作者还检索了Cochrane对照试验中央注册库(CENTRAL)(《Cochrane图书馆》2004年第3期)、MEDLINE(1966年至2004年8月)、EMBASE(1980年至2004年6月)、AMED(1985年至2002年5月)以及中国生物医学数据库(CBM磁盘,1979年至2004年8月)。作者检索了相关临床试验和研究注册库,并联系了制药公司和研究人员,以识别更多已发表和未发表的研究。

选择标准

比较银杏叶提取物与安慰剂或开放对照(无安慰剂)用于急性缺血性中风患者的随机对照试验或半随机对照临床试验。

数据收集与分析

两名作者独立选择纳入试验、评估试验质量并提取数据。

主要结果

共识别出14项试验,其中10项试验(792例患者)被纳入。4项试验等待评估。在10项纳入试验中,中风后14至35天进行随访。所有研究均评估了神经学结局,但均未报告残疾情况(日常生活活动功能)或生活质量。只有3项试验报告了不良事件。在9项试验中,所有试验质量均被评估为较差,以治疗结束时神经功能缺损的显著改善作为结局指标。对这些试验进行综合分析时,银杏叶提取物与改善患者数量的显著增加相关(Peto比值比(OR)2.66;95%置信区间(CI):1.79 - 3.94)。一项质量评估为良好的安慰剂对照试验将神经学结局作为连续变量报告。该试验未显示治疗结束时神经功能缺损有所改善(加权平均差(固定效应)0.81;95%CI: - 8.9 - 10.52)。随访期间未报告死亡或重大不良事件。

结论

方法学质量充分的试验中没有令人信服的证据支持常规使用银杏叶提取物促进中风后恢复。需要高质量和大规模的随机对照试验来检验其疗效。

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