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非侵入性迷走神经刺激治疗发作性和慢性丛集性头痛急性发作的疗效差异:一项荟萃分析。

Differential efficacy of non-invasive vagus nerve stimulation for the acute treatment of episodic and chronic cluster headache: A meta-analysis.

机构信息

1 Leiden University Medical Centre, Leiden, the Netherlands.

2 NIHR-Wellcome Trust King's Clinical Research Facility, King's College London, UK.

出版信息

Cephalalgia. 2019 Jul;39(8):967-977. doi: 10.1177/0333102419856607. Epub 2019 Jun 10.

Abstract

BACKGROUND

Two randomized, double-blind, sham-controlled trials (ACT1, ACT2) evaluated non-invasive vagus nerve stimulation (nVNS) as acute treatment for cluster headache. We analyzed pooled ACT1/ACT2 data to increase statistical power and gain insight into the differential efficacy of nVNS in episodic and chronic cluster headache.

METHODS

Data extracted from ACT1 and ACT2 were pooled using a fixed-effects model. Main outcome measures were the primary endpoints of each study. This was the proportion of participants whose first treated attack improved from moderate (2), severe (3), or very severe (4) pain intensity to mild (1) or nil (0) for ACT1 and the proportion of treated attacks whose pain intensity improved from 2-4 to 0 for ACT2.

RESULTS

The pooled population included 225 participants (episodic: n = 112; chronic: n = 113) from ACT1 (n = 133) and ACT2 (n = 92) in the nVNS (n = 108) and sham (n = 117) groups. Interaction was shown between treatment group and cluster headache subtype ( < 0.05). nVNS was superior to sham in episodic but not chronic cluster headache (both endpoints  < 0.01). Only four patients discontinued the studies due to adverse events.

CONCLUSIONS

nVNS is a well-tolerated and effective acute treatment for episodic cluster headache.

TRIAL REGISTRATION

The studies were registered at clinicaltrials.gov (ACT1: NCT01792817; ACT2: NCT01958125).

摘要

背景

两项随机、双盲、假对照试验(ACT1、ACT2)评估了非侵入性迷走神经刺激(nVNS)作为丛集性头痛的急性治疗方法。我们对 ACT1/ACT2 的汇总数据进行了分析,以增加统计效力,并深入了解 nVNS 在发作性和慢性丛集性头痛中的差异疗效。

方法

使用固定效应模型对从 ACT1 和 ACT2 中提取的数据进行汇总。主要观察指标为每项研究的主要终点。这是 ACT1 中首次治疗攻击的参与者比例,从中度(2)、重度(3)或非常重度(4)疼痛强度改善为轻度(1)或无(0),对于 ACT2,从 2-4 到 0 改善的治疗攻击比例。

结果

汇总人群包括来自 ACT1(n=133)和 ACT2(n=92)的 nVNS(n=108)和假对照(n=117)组的 225 名参与者(发作性:n=112;慢性:n=113)。治疗组与丛集性头痛亚型之间存在交互作用( < 0.05)。nVNS 在发作性但不在慢性丛集性头痛中优于假对照(两个终点均 < 0.01)。仅有 4 名患者因不良事件而退出研究。

结论

nVNS 是一种耐受良好且有效的发作性丛集性头痛急性治疗方法。

试验注册

这些研究在 clinicaltrials.gov 上注册(ACT1:NCT01792817;ACT2:NCT01958125)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ec0/6637721/da0683072370/10.1177_0333102419856607-fig1.jpg

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