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急性缺血性脑卒中的血管内再通治疗:随机对照试验的更新荟萃分析。

Endovascular Recanalization Therapy in Acute Ischemic Stroke: Updated Meta-analysis of Randomized Controlled Trials.

机构信息

Department of Neurology, Inje University Ilsan Paik Hospital, Goyang, Korea.

Department of Neurology, Seoul National University College of Medicine, Seoul, Korea.

出版信息

J Stroke. 2015 Sep;17(3):268-81. doi: 10.5853/jos.2015.17.3.268. Epub 2015 Sep 30.

Abstract

BACKGROUND AND PURPOSE

Recent randomized clinical trials (RCTs) have demonstrated benefits of endovascular recanalization therapy (ERT) contrary to earlier trials. We aimed to estimate the benefits of ERT added to standard therapy in acute ischemic stroke.

METHODS

From a literature search of RCTs testing ERT, we performed a meta-analysis to estimate an overall efficacy and safety of ERT for all trials, stent-retriever trials, and RCTs comparing ERT and intravenous tissue plasminogen activator (IV-TPA).

RESULTS

We identified 15 relevant RCTs including 2,899 patients. For all trials, ERT was associated with increased good outcomes (odds ratio [OR] 1.79; 95% confidence interval [CI] 1.34, 2.40; P<0.001) compared to the control. ERT also increased no or minimal disability outcomes, good neurological recovery, good activity of daily living, and recanalization. ERT did not significantly increase symptomatic intracranial hemorrhage (SICH) (OR 1.19; 95% CI 0.83, 1.69; P=0.345) or death (OR 0.87; 95% CI 0.71, 1.05; P=0.151). In contrast, ERT significantly reduced extreme disability or death (OR 0.77; 95% CI 0.61, 0.97; P=0.025). Restricting to five stent-retriever trials comparing ERT plus IV-TPA vs. IV-TPA alone, the benefit was even greater for good outcome (OR 2.39; 95% CI 1.88, 3.04; P<0.001) and extreme disability or death (OR 0.57; 95% CI 0.41, 0.78; P=0.001). Restricting to eight RCTs comparing ERT (plus IV-TPA in six trials) with IV-TPA alone showed similar efficacy and safety.

CONCLUSIONS

This updated meta-analysis shows that ERT substantially improves clinical outcomes and reduces extreme disability or death without significantly increasing SICH compared to standard therapy.

摘要

背景与目的

最近的随机临床试验(RCT)表明,血管内再通治疗(ERT)的疗效优于早期试验。我们旨在评估 ERT 联合标准治疗对急性缺血性脑卒中的疗效。

方法

我们从测试 ERT 的 RCT 文献检索中进行了荟萃分析,以估计所有试验、支架取栓试验以及比较 ERT 和静脉组织型纤溶酶原激活剂(IV-TPA)的 RCT 的 ERT 的总体疗效和安全性。

结果

我们确定了 15 项相关的 RCT,包括 2899 名患者。与对照组相比,ERT 可增加所有试验的良好结局(优势比[OR]1.79;95%置信区间[CI]1.34-2.40;P<0.001)。ERT 还增加了无残疾或轻度残疾、良好神经恢复、良好日常生活活动和再通。ERT 并未显著增加症状性颅内出血(SICH)(OR 1.19;95%CI 0.83-1.69;P=0.345)或死亡(OR 0.87;95%CI 0.71-1.05;P=0.151)。相反,ERT 显著降低了极度残疾或死亡(OR 0.77;95%CI 0.61-0.97;P=0.025)。将范围限制在五项比较 ERT 加 IV-TPA 与 IV-TPA 单独治疗的支架取栓试验中,良好结局(OR 2.39;95%CI 1.88-3.04;P<0.001)和极度残疾或死亡(OR 0.57;95%CI 0.41-0.78;P=0.001)的获益更大。将范围限制在八项比较 ERT(六项试验中加 IV-TPA)与 IV-TPA 单独治疗的 RCT 中,显示出相似的疗效和安全性。

结论

本更新的荟萃分析表明,与标准治疗相比,ERT 可显著改善临床结局并降低极度残疾或死亡的风险,而不会显著增加 SICH。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbf5/4635708/d8f2c4eb771a/jos-17-3-268f1.jpg

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