Thrombolysis for aneurysmal subarachnoid haemorrhage.

IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Cochrane Database of Systematic Reviews Pub Date : 2025-01-17 DOI:10.1002/14651858.CD013748.pub2
Edward R Bader, Mazen M Allam, Thomas Gw Harris, Neena Suchdev, Yoon Kong Loke, Raphae Barlas
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Trials investigating local administration of thrombolytics have reported promising results.</p><p><strong>Objectives: </strong>- To assess the effect of thrombolysis on improving functional outcome and case fatality following aneurysmal subarachnoid haemorrhage - To determine the effect of thrombolysis on the risk of cerebral artery vasospasm, delayed cerebral ischaemia, and hydrocephalus following subarachnoid haemorrhage - To determine the risk of complications of local thrombolysis in aneurysmal subarachnoid haemorrhage SEARCH METHODS: We searched the Cochrane Central Register of Controlled Trials (last searched 9 March 2023), MEDLINE Ovid (1946 to 9 March 2023), and Embase Ovid (1974 to 9 March 2023). We also searched ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform (ICTRP). We performed forward and reverse citation tracking of included studies using Google Scholar.</p><p><strong>Selection criteria: </strong>We included randomised controlled trials comparing subarachnoid thrombolysis via any route of administration into any anatomical site continuous with the subarachnoid space versus placebo, sham thrombolysis, or standard treatment.</p><p><strong>Data collection and analysis: </strong>Two review authors independently selected studies for inclusion in the review. We extracted study data and used version 2 of the Cochrane risk-of-bias tool for randomised trials to assess the risk of bias in the studies. We resolved any disagreement through discussion with a third author. Our primary outcome was poor functional outcome. Secondary outcomes were case fatality, haemorrhagic complications, cerebral artery vasospasm, delayed cerebral ischaemia, cerebral infarction, and hydrocephalus. We performed meta-analyses for each outcome and performed sensitivity analysis excluding studies at high risk of bias. We presented results as risk ratios (RRs) with 95% confidence intervals (CIs). We performed further sensitivity analysis by including all intervention groups from studies reporting more than one intervention group. For each outcome, we used the GRADE criteria to determine the certainty of the evidence.</p><p><strong>Main results: </strong>We included eight studies from six countries in this review. The studies had a total of 410 participants, of whom 205 received thrombolysis. We identified three ongoing trials. We assessed one trial as having a high risk of bias for all outcomes; we assessed the remainder as having a low risk of bias or some concerns. Thrombolysis likely results in a reduction in poor functional outcome when compared to placebo or standard care (29.4% versus 39.7%, RR 0.73, 95% CI 0.56 to 0.94; 8 studies, 408 participants; moderate-certainty evidence). Thrombolysis likely results in little to no difference in case fatality (12.8% versus 17.7%, RR 0.71, 95% CI 0.46 to 1.10; 8 studies, 408 participants; moderate-certainty evidence). Thrombolysis may result in little to no difference in haemorrhagic complications (10.3% versus 7.2%, RR 1.40, 95% CI 0.73 to 2.68; 6 studies, 341 participants; low-certainty evidence). Thrombolysis likely results in a reduction in cerebral artery vasospasm (32.9% versus 47.6%, RR 0.70, 95% CI 0.54 to 0.91; studies, participants; moderate-certainty evidence), and may result in a reduction in delayed cerebral ischaemia (23.8% versus 38.2%, RR 0.62, 95% CI 0.45 to 0.88; studies, participants; low-certainty evidence). Thrombolysis may result in little to no difference in cerebral infarction (28.6% versus 37.5%, RR 0.76, 95% CI 0.44 to 1.31; studies, participants; low-certainty evidence), and likely results in little to no difference in the risk of hydrocephalus (18.3% versus 24.1%, RR 0.77, 95% CI 0.54 to 1.10; studies, participants; moderate-certainty evidence).</p><p><strong>Authors' conclusions: </strong>There is some evidence that thrombolysis can probably improve outcomes after aneurysmal subarachnoid haemorrhage, without increasing the risk of haemorrhagic complications. Thrombolysis likely reduces the risk of poor functional outcome and cerebral artery vasospasm, and may reduce the risk of delayed cerebral ischaemia, but it likely makes little to no difference to case fatality or hydrocephalus, and may make little to no difference to the risk of cerebral infarction. However, the current evidence is still uncertain. 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引用次数: 0

Abstract

Background: Aneurysmal subarachnoid haemorrhage continues to cause a significant burden of morbidity and mortality despite advances in care. Trials investigating local administration of thrombolytics have reported promising results.

Objectives: - To assess the effect of thrombolysis on improving functional outcome and case fatality following aneurysmal subarachnoid haemorrhage - To determine the effect of thrombolysis on the risk of cerebral artery vasospasm, delayed cerebral ischaemia, and hydrocephalus following subarachnoid haemorrhage - To determine the risk of complications of local thrombolysis in aneurysmal subarachnoid haemorrhage SEARCH METHODS: We searched the Cochrane Central Register of Controlled Trials (last searched 9 March 2023), MEDLINE Ovid (1946 to 9 March 2023), and Embase Ovid (1974 to 9 March 2023). We also searched ClinicalTrials.gov and the WHO International Clinical Trials Registry Platform (ICTRP). We performed forward and reverse citation tracking of included studies using Google Scholar.

Selection criteria: We included randomised controlled trials comparing subarachnoid thrombolysis via any route of administration into any anatomical site continuous with the subarachnoid space versus placebo, sham thrombolysis, or standard treatment.

Data collection and analysis: Two review authors independently selected studies for inclusion in the review. We extracted study data and used version 2 of the Cochrane risk-of-bias tool for randomised trials to assess the risk of bias in the studies. We resolved any disagreement through discussion with a third author. Our primary outcome was poor functional outcome. Secondary outcomes were case fatality, haemorrhagic complications, cerebral artery vasospasm, delayed cerebral ischaemia, cerebral infarction, and hydrocephalus. We performed meta-analyses for each outcome and performed sensitivity analysis excluding studies at high risk of bias. We presented results as risk ratios (RRs) with 95% confidence intervals (CIs). We performed further sensitivity analysis by including all intervention groups from studies reporting more than one intervention group. For each outcome, we used the GRADE criteria to determine the certainty of the evidence.

Main results: We included eight studies from six countries in this review. The studies had a total of 410 participants, of whom 205 received thrombolysis. We identified three ongoing trials. We assessed one trial as having a high risk of bias for all outcomes; we assessed the remainder as having a low risk of bias or some concerns. Thrombolysis likely results in a reduction in poor functional outcome when compared to placebo or standard care (29.4% versus 39.7%, RR 0.73, 95% CI 0.56 to 0.94; 8 studies, 408 participants; moderate-certainty evidence). Thrombolysis likely results in little to no difference in case fatality (12.8% versus 17.7%, RR 0.71, 95% CI 0.46 to 1.10; 8 studies, 408 participants; moderate-certainty evidence). Thrombolysis may result in little to no difference in haemorrhagic complications (10.3% versus 7.2%, RR 1.40, 95% CI 0.73 to 2.68; 6 studies, 341 participants; low-certainty evidence). Thrombolysis likely results in a reduction in cerebral artery vasospasm (32.9% versus 47.6%, RR 0.70, 95% CI 0.54 to 0.91; studies, participants; moderate-certainty evidence), and may result in a reduction in delayed cerebral ischaemia (23.8% versus 38.2%, RR 0.62, 95% CI 0.45 to 0.88; studies, participants; low-certainty evidence). Thrombolysis may result in little to no difference in cerebral infarction (28.6% versus 37.5%, RR 0.76, 95% CI 0.44 to 1.31; studies, participants; low-certainty evidence), and likely results in little to no difference in the risk of hydrocephalus (18.3% versus 24.1%, RR 0.77, 95% CI 0.54 to 1.10; studies, participants; moderate-certainty evidence).

Authors' conclusions: There is some evidence that thrombolysis can probably improve outcomes after aneurysmal subarachnoid haemorrhage, without increasing the risk of haemorrhagic complications. Thrombolysis likely reduces the risk of poor functional outcome and cerebral artery vasospasm, and may reduce the risk of delayed cerebral ischaemia, but it likely makes little to no difference to case fatality or hydrocephalus, and may make little to no difference to the risk of cerebral infarction. However, the current evidence is still uncertain. The uncertainty is primarily due to the small total number of participants and outcome events. Data from further studies are required to confirm the efficacy of thrombolysis for improving outcomes after aneurysmal subarachnoid haemorrhage.

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动脉瘤性蛛网膜下腔出血的溶栓治疗。
背景:尽管治疗取得了进步,动脉瘤性蛛网膜下腔出血仍然是发病率和死亡率的重要负担。研究溶栓药物局部管理的试验报告了有希望的结果。目的:评估溶栓对改善动脉瘤性蛛网膜下腔出血后功能结局和病死率的影响;确定溶栓对动脉瘤性蛛网膜下腔出血后脑动脉痉挛、迟发性脑缺血和脑积水风险的影响;确定动脉瘤性蛛网膜下腔出血局部溶栓并发症的风险。我们检索了Cochrane中央对照试验注册库(最后检索日期为2023年3月9日)、MEDLINE Ovid(1946年至2023年3月9日)和Embase Ovid(1974年至2023年3月9日)。我们还检索了ClinicalTrials.gov和WHO国际临床试验注册平台(ICTRP)。我们使用谷歌Scholar对纳入的研究进行了正向和反向引文跟踪。选择标准:我们纳入了随机对照试验,比较蛛网膜下腔溶栓通过任何给药途径进入蛛网膜下腔的任何解剖部位与安慰剂、假溶栓或标准治疗。资料收集和分析:两位综述作者独立选择研究纳入综述。我们提取研究数据,并使用Cochrane随机试验风险偏倚工具第2版来评估研究的偏倚风险。我们通过与第三作者讨论来解决任何分歧。我们的主要结果是功能不良。次要结局是病死率、出血性并发症、脑动脉血管痉挛、迟发性脑缺血、脑梗死和脑积水。我们对每个结果进行了荟萃分析,并进行了敏感性分析,排除了高偏倚风险的研究。我们以95%置信区间(ci)的风险比(rr)来呈现结果。我们通过纳入来自多个干预组的研究的所有干预组,进行了进一步的敏感性分析。对于每个结果,我们使用GRADE标准来确定证据的确定性。主要结果:我们纳入了来自6个国家的8项研究。这些研究共有410名参与者,其中205人接受了溶栓治疗。我们确定了三个正在进行的试验。我们将一项试验评估为所有结果具有高偏倚风险;我们将其余的评估为低偏倚风险或存在一些问题。与安慰剂或标准治疗相比,溶栓可能导致功能不良结局的减少(29.4%对39.7%,RR 0.73, 95% CI 0.56 ~ 0.94;8项研究,408名参与者;moderate-certainty证据)。溶栓可能导致病死率几乎没有差异(12.8%对17.7%,RR 0.71, 95% CI 0.46 ~ 1.10;8项研究,408名参与者;moderate-certainty证据)。溶栓可能导致出血性并发症的差异很小或没有差异(10.3%对7.2%,RR 1.40, 95% CI 0.73至2.68;6项研究,341名参与者;确定性的证据)。溶栓可能导致脑动脉血管痉挛减少(32.9%对47.6%,RR 0.70, 95% CI 0.54 ~ 0.91;研究中,参与者;中度确定性证据),并可能导致迟发性脑缺血减少(23.8%对38.2%,RR 0.62, 95% CI 0.45 ~ 0.88;研究中,参与者;确定性的证据)。溶栓可能导致脑梗死几乎没有差异(28.6%对37.5%,RR 0.76, 95% CI 0.44 ~ 1.31;研究中,参与者;低确定性证据),并且可能导致脑积水的风险几乎没有差异(18.3%对24.1%,RR 0.77, 95% CI 0.54至1.10;研究中,参与者;moderate-certainty证据)。作者的结论:有证据表明溶栓可能改善动脉瘤性蛛网膜下腔出血后的预后,而不会增加出血并发症的风险。溶栓可能降低功能预后不良和脑动脉痉挛的风险,并可能降低迟发性脑缺血的风险,但可能对病死率或脑积水几乎没有影响,对脑梗死的风险几乎没有影响。然而,目前的证据仍然不确定。不确定性主要是由于参与者和结果事件的总数较少。需要进一步的研究数据来证实溶栓对改善动脉瘤性蛛网膜下腔出血后预后的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.60
自引率
2.40%
发文量
173
审稿时长
1-2 weeks
期刊介绍: The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.
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