超声引导下颈上神经节阻滞治疗偏头痛:一项倾向评分匹配的回顾性研究。

IF 2.5 Q2 CLINICAL NEUROLOGY
Frontiers in pain research (Lausanne, Switzerland) Pub Date : 2025-08-28 eCollection Date: 2025-01-01 DOI:10.3389/fpain.2025.1556654
Wenxing Zhao, Hong Yue, Liqiang Yang, Liangliang He
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引用次数: 0

摘要

背景:本研究旨在探讨超声(US)引导下颈上神经节(SCG)阻滞联合标准曲坦治疗偏头痛发作的疗效和安全性。方法:共有243名患者在偏头痛发作时接受辅助us引导SCG阻滞和曲坦类药物作为SCG队列。基于基线协变量的1:1倾向评分用于匹配243例单独接受曲坦类药物作为对照的病例。主要终点是术后24小时内疼痛缓解和疼痛解除。次要结局包括2小时内头痛缓解和疼痛缓解、每月偏头痛天数(MMDs)、偏头痛残疾评估(MIDAS)评分、偏头痛特异性生活质量问卷(MSQ)评分和不良事件。结果:与对照组相比,SCG组24 h疼痛缓解率和疼痛解除率均增加[73.3%比49.4%,平均差异[MD]分别为23.9%[95%可信区间(CI): 15.5% ~ 29.0%]和64.2%比37.4%,MD = 26.7% [95% CI: 18.2% ~ 31.3%]]。由于95% CI在15%的优势范围内,达到了优势。在SCG队列中,手术后2小时疼痛缓解率和疼痛缓解率更高(p p p = 0.040), MSQ评分(p = 0.036)。SCG组无严重不良事件发生。结论:在1个月的随访中,美国引导的曲坦类SCG阻滞在偏头痛发作期间达到长达24小时的头痛缓解方面优于曲坦类单独治疗,导致偏头痛天数减少,功能能力和生活质量得到改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ultrasound-guided block of the superior cervical ganglion for migraine attacks: a propensity score-matched retrospective study.

Ultrasound-guided block of the superior cervical ganglion for migraine attacks: a propensity score-matched retrospective study.

Ultrasound-guided block of the superior cervical ganglion for migraine attacks: a propensity score-matched retrospective study.

Ultrasound-guided block of the superior cervical ganglion for migraine attacks: a propensity score-matched retrospective study.

Background: This study aimed to examine the efficacy and safety of ultrasound (US)-guided superior cervical ganglion (SCG) block in conjunction with standard triptan in the management of migraine attacks.

Methods: In total, 243 subjects who received an adjunctive US-guided SCG block alongside triptan for a migraine attack were enrolled as the SCG cohort. A 1:1 propensity score based on baseline covariates was used to match 243 cases who received triptan alone as the control. The primary endpoints were pain relief and freedom from pain within 24 h after the procedure. Secondary outcomes included headache relief and freedom from pain within 2 h, monthly migraine days (MMDs), Migraine Disability Assessment (MIDAS) scores, Migraine-Specific Quality of Life questionnaire (MSQ) scores, and adverse events.

Results: The rates of pain relief and freedom from pain at 24 h after the block were increased in the SCG cases compared to the controls {73.3% vs. 49.4%, with mean difference [MD] of 23.9% [95% confidence interval (CI): 15.5%-29.0%] and 64.2% vs. 37.4%, with MD = 26.7% [95% CI: 18.2%-31.3%], respectively}. Superiority was met, as the 95% CI fell within the superiority margin of 15%. Higher rates of pain relief and freedom from pain at 2 h following the procedure were reported in the SCG cohort (both p < 0.001). At the 1-month follow-up, the SCG cohort had a greater improvement in MMDs (p < 0.01), MIDAS scores (p = 0.040), and MSQ scores (p = 0.036). There were no severe adverse events in the SCG group.

Conclusions: US-guided SCG block with triptan was superior to triptan alone in achieving headache remission during a migraine attack for up to 24 h, resulting in reduced migraine days and improved functional ability and life quality at the 1-month follow-up.

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