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经颅激光治疗急性缺血性卒中

Transcranial laser therapy for acute ischaemic stroke.

作者信息

He Haoyang, Zhang Zhimeng, Chen Hengshu, Jiang Zhixuan, Wang Yanan, Song Xindi, Liu Junfeng, Wu Simiao

机构信息

Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.

Centre of Cerebrovascular Diseases, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Cochrane Database Syst Rev. 2025 Jul 24;7:CD012426. doi: 10.1002/14651858.CD012426.pub2.

Abstract

RATIONALE

Ischaemic stroke is a leading cause of disability and death worldwide, but limited treatment options are available to improve its outcomes. Some studies have explored transcranial laser therapy in people with acute ischaemic stroke, but the benefits and harms of this treatment are unclear.

OBJECTIVES

The primary objective was to assess the benefits and harms of transcranial laser therapy for improving functional outcomes after acute ischaemic stroke. The secondary objective was to assess the equity of transcranial laser therapy in people with acute ischaemic stroke.

SEARCH METHODS

We searched CENTRAL, MEDLINE, Embase, ISI Science Citation Index, CINAHL, PEDro (Physiotherapy Evidence Database), REHABDATA, and four ongoing trials registries. We also searched reference lists and databases of conference abstracts for other studies, including any that are ongoing or unpublished. The latest search date was 3 August 2024 for all databases except CenterWatch, which we searched on 1 November 2024.

ELIGIBILITY CRITERIA

We included randomised controlled trials (RCTs) comparing transcranial laser therapy with sham treatment or no treatment in people with acute ischaemic stroke, with or without standard treatment in both groups.

OUTCOMES

The critical outcomes were unfavourable functional outcome, defined as a score of 3 to 6 on the modified Rankin Scale (mRS), and all-cause mortality. The important outcomes were improvement of stroke severity measured on the National Institutes of Health Stroke Scale (NIHSS), serious adverse events, and adverse events.

RISK OF BIAS

We used the Cochrane risk of bias tool (RoB 2) to assess the risk of bias for all outcomes in all RCTs.

SYNTHESIS METHODS

We planned to use risk ratios (RRs) with 95% confidence intervals (CIs) to compare all outcomes. However, for improvement of stroke severity, we extracted odds ratios (ORs) and 95% CIs from the original studies because the raw data were unavailable. Our meta-analyses used fixed-effect modelling. To assess statistical heterogeneity, we used the I statistic. We used the GRADE approach to assess the certainty of the evidence.

INCLUDED STUDIES

We included four RCTs enrolling a total of 1420 people with acute ischaemic stroke. The studies were published between 2007 and 2014. All were multicentre studies, based in Europe, North America, South America, Asia, or more than one of these continents. All studies included people older than 40 years (mean age 68.3 years), and 59.6% of participants were men. All studies enrolled participants within 24 hours after onset of stroke symptoms, all used a transcranial laser of 808-nm wavelength, and all compared transcranial laser therapy with sham treatment.

SYNTHESIS OF RESULTS

Critical outcomes Transcranial laser therapy results in little to no difference in unfavourable functional outcome at 90 days compared with sham treatment (RR 0.93, 95% CI 0.85 to 1.02; I² = 10%; 3 studies, 1408 participants; high-certainty evidence). Transcranial laser therapy may result in little to no difference in all-cause mortality at 90 days compared with sham treatment (RR 0.96, 95% CI 0.72 to 1.28; I² = 0%; 4 studies, 1420 participants; low-certainty evidence). Important outcomes Transcranial laser therapy may result in little to no difference in improvement of stroke severity at 90 days compared with sham treatment (OR 1.14, 95% CI 0.92 to 1.42; I² = 73%; 3 studies, 1408 participants; low-certainty evidence). Transcranial laser therapy may lead to a slight reduction in serious adverse events at 90 days compared with sham treatment (RR 0.83, 95% CI 0.71 to 0.96; I² = 0%; 4 studies, 1420 participants; low-certainty evidence). Transcranial laser therapy likely results in little to no difference in adverse events at 90 days compared with sham treatment (RR 1.01, 95% CI 0.97 to 1.06; I² = 8%; 3 studies, 1300 participants; moderate-certainty evidence). After excluding the only study with high risk of bias judgements, the findings of sensitivity analyses for unfavourable functional outcome, improvement of stroke severity, and serious adverse events were consistent with the findings of the main analyses. For serious adverse events, we excluded the only study (630 participants) with positive findings, and the pooled effect estimate of the remaining three studies indicated little or no difference between the intervention and control groups.

AUTHORS' CONCLUSIONS: The current evidence shows no clear benefit or harm associated with transcranial laser therapy in people with acute ischaemic stroke. Our results suggest transcranial laser therapy compared with sham treatment results in little to no difference in unfavourable functional outcome and may result in little to no difference in all-cause mortality at 90 days. The evidence regarding adverse events was of low-to-moderate certainty. More high-quality trials are needed to further evaluate the role of transcranial laser therapy in people with acute ischaemic stroke, to inform the optimal treatment regimen, and to identify people who might benefit most from the therapy.

FUNDING

This review was supported by the National Natural Science Foundation of China (grant numbers 82171285; 82371323); the Science and Technology Department of Sichuan Province (grant numbers 2024YFHZ0330; 2023NSFSC1558); the 1·3·5 project for disciplines of excellence-Clinical Research Fund, West China Hospital, Sichuan University (grant numbers 2024HXFH022; 2024HXFH023); and the Postdoctor Research Fund of West China Hospital, Sichuan University (grant number 2024HXBH139).

REGISTRATION

Protocol available via DOI: 10.1002/14651858.CD012426.

摘要

理论依据

缺血性中风是全球致残和致死的主要原因之一,但改善其预后的治疗选择有限。一些研究探索了经颅激光疗法对急性缺血性中风患者的疗效,但这种治疗的利弊尚不清楚。

目的

主要目的是评估经颅激光疗法对改善急性缺血性中风后功能预后的利弊。次要目的是评估经颅激光疗法在急性缺血性中风患者中的公平性。

检索方法

我们检索了Cochrane系统评价数据库、医学期刊数据库、荷兰医学文摘数据库、科学引文索引、护理学与健康领域数据库、物理治疗循证数据库、康复数据库以及四个正在进行的试验注册库。我们还检索了参考文献列表和会议摘要数据库以查找其他研究,包括正在进行或未发表的研究。除CenterWatch于2024年11月1日检索外,所有数据库的最新检索日期为2024年8月3日。

纳入标准

我们纳入了随机对照试验,这些试验比较了经颅激光疗法与假治疗或不治疗对急性缺血性中风患者的效果,两组均接受或不接受标准治疗。

结局指标

关键结局指标为不良功能结局,定义为改良Rankin量表(mRS)评分为3至6分,以及全因死亡率。重要结局指标为根据美国国立卫生研究院卒中量表(NIHSS)测量的中风严重程度改善情况、严重不良事件和不良事件。

偏倚风险

我们使用Cochrane偏倚风险工具(RoB 2)评估所有随机对照试验中所有结局指标的偏倚风险。

合成方法

我们计划使用风险比(RR)及95%置信区间(CI)来比较所有结局指标。然而,对于中风严重程度的改善情况(由于原始数据不可用),我们从原始研究中提取了比值比(OR)及95%CI。我们的荟萃分析采用固定效应模型。为评估统计异质性,我们使用I²统计量。我们采用GRADE方法评估证据的确定性。

纳入研究

我们纳入了四项随机对照试验,共招募了1420例急性缺血性中风患者。这些研究发表于2007年至2014年之间。所有研究均为多中心研究,分布在欧洲、北美洲、南美洲、亚洲或多个大洲。所有研究纳入的患者年龄均超过40岁(平均年龄68.3岁),59.6%的参与者为男性。所有研究均在中风症状发作后24小时内招募参与者,均使用808纳米波长的经颅激光,且均将经颅激光疗法与假治疗进行比较。

结果合成

关键结局指标:与假治疗相比,经颅激光疗法在90天时不良功能结局的差异很小或无差异(RR 0.93,95%CI 0.85至1.02;I² = 10%;3项研究,1408名参与者;高确定性证据)。与假治疗相比,经颅激光疗法在90天时全因死亡率的差异可能很小或无差异(RR 0.96,95%CI 0.72至1.28;I² = 0%;4项研究,1420名参与者;低确定性证据)。重要结局指标:与假治疗相比,经颅激光疗法在90天时中风严重程度改善情况的差异可能很小或无差异(OR 1.14,95%CI 0.92至1.42;I² = 73%;3项研究,1408名参与者;低确定性证据)。与假治疗相比,经颅激光疗法在90天时可能会使严重不良事件略有减少(RR 0.83,95%CI 0.71至0.96;I² = 0%;4项研究,1420名参与者;低确定性证据)。与假治疗相比,经颅激光疗法在90天时不良事件的差异可能很小或无差异(RR 1.01,95%CI 0.97至1.06;I² = 8%;3项研究,1300名参与者;中等确定性证据)。在排除唯一一项具有高偏倚风险判断的研究后,对不良功能结局、中风严重程度改善情况和严重不良事件的敏感性分析结果与主要分析结果一致。对于严重不良事件,我们排除了唯一一项有阳性结果的研究(630名参与者),其余三项研究的合并效应估计表明干预组和对照组之间几乎没有差异。

作者结论

目前的证据表明,经颅激光疗法对急性缺血性中风患者没有明显的益处或危害。我们的结果表明,与假治疗相比,经颅激光疗法在90天时不良功能结局的差异很小或无差异,全因死亡率的差异可能也很小或无差异。关于不良事件的证据确定性为低到中等。需要更多高质量的试验来进一步评估经颅激光疗法在急性缺血性中风患者中的作用,以确定最佳治疗方案,并识别可能从该疗法中获益最大的人群。

资助

本综述得到了中国国家自然科学基金(项目编号82171285;82371323)、四川省科学技术厅(项目编号2024YFHZ0330;2023NSFSC1558)、四川大学华西医院卓越学科1·3·5项目 - 临床研究基金(项目编号2024HXFH022;2024HXFH023)以及四川大学华西医院博士后研究基金(项目编号2024HXBH139)的支持。

注册

方案可通过DOI:10.1002/14651858.CD012426获取。

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