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欧洲头痛联盟(EHF)对偏头痛预防中口服药物的关键重新评估和荟萃分析 - 第 3 部分:托吡酯。

European Headache Federation (EHF) critical reappraisal and meta-analysis of oral drugs in migraine prevention - part 3: topiramate.

机构信息

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Clinician Scientist Program, Berlin Institute of Health at Charité (BIH), Berlin, Germany.

出版信息

J Headache Pain. 2023 Oct 10;24(1):134. doi: 10.1186/s10194-023-01671-5.

Abstract

OBJECTIVE

Topiramate is a repurposed first-line treatment for migraine prophylaxis. The aim of this systematic review and meta-analysis is to critically re-appraise the existing evidence supporting the efficacy and tolerability of topiramate.

METHODS

A systematic search in MEDLINE, EMBASE, Cochrane CENTRAL, and ClinicalTrials.gov was performed for trials of pharmacological treatment in migraine prophylaxis as of August 13, 2022, following the Preferred Reporting Items for Systematic Reviews (PRISMA). Randomized controlled trials in adult patients that used topiramate for the prophylactic treatment of migraine, with placebo as active comparator, were included. Two reviewers independently screened the retrieved studies and extracted all data. Outcomes of interest were the 50% responder rates, the reduction in monthly migraine days, and adverse events leading to treatment discontinuation. Results were pooled and meta-analyzed, with sensitivity analysis based on the risk of bias of the studies, the monthly migraine days at baseline, and the previous use of other prophylactic treatments. Certainty evidence was judged according to the GRADE framework.

RESULTS

Eight out of 10,826 studies fulfilled the inclusion/exclusion criteria, accounting for 2,610 randomized patients. Six studies included patients with episodic migraine and two with chronic migraine. Topiramate dose ranged from 50 to 200 mg/day, and all studies included a placebo arm. There was a high certainty that topiramate: 1) increased the proportion of patients who achieved a 50% responder rate in monthly migraine days, compared to placebo [relative risk: 1.61 (95% confidence interval (CI): 1.29-2.01); absolute risk difference: 168 more per 1,000 (95% CI: 80 to 278 more)]; 2) was associated with 0.99 (95% CI: 1.41-0.58) fewer migraine days than placebo; 3) and had a higher proportion of patients with adverse events leading to treatment discontinuation [absolute risk difference 80 patients more per 1,000 (95% CI: 20 to 140 more patients)].

CONCLUSIONS

There is high-quality evidence of the efficacy of topiramate in the prophylaxis of migraine, albeit its use poses a risk of adverse events that may lead to treatment discontinuation, with a negative effect on patient satisfaction and adherence to care.

摘要

目的

托吡酯是一种重新定位的偏头痛预防一线治疗药物。本系统评价和荟萃分析的目的是批判性地重新评估支持托吡酯疗效和耐受性的现有证据。

方法

截至 2022 年 8 月 13 日,在 MEDLINE、EMBASE、Cochrane CENTRAL 和 ClinicalTrials.gov 中进行了药物治疗偏头痛预防的系统搜索,遵循系统评价的首选报告项目 (PRISMA)。纳入了使用托吡酯预防性治疗偏头痛的成年患者的随机对照试验,以安慰剂作为活性对照。两名评审员独立筛选检索到的研究并提取所有数据。主要观察指标为 50%应答率、每月偏头痛天数减少以及导致治疗中断的不良事件。结果进行汇总和荟萃分析,基于研究的偏倚风险、基线时每月偏头痛天数和以前使用其他预防性治疗进行敏感性分析。根据 GRADE 框架判断确定性证据。

结果

在 10826 项研究中,有 8 项符合纳入/排除标准,共纳入 2610 名随机患者。其中 6 项研究纳入了发作性偏头痛患者,2 项研究纳入了慢性偏头痛患者。托吡酯剂量范围为 50-200mg/天,所有研究均包含安慰剂组。有高质量证据表明,与安慰剂相比,托吡酯:1)增加了每月偏头痛天数达到 50%应答率的患者比例[相对风险:1.61(95%置信区间(CI):1.29-2.01);绝对风险差异:每 1000 人增加 168 人(95%CI:80 至 278 人)];2)与安慰剂相比,偏头痛天数减少 0.99(95%CI:1.41-0.58);3)导致治疗中断的不良事件发生率更高[绝对风险差异每 1000 人增加 80 人(95%CI:20 至 140 人)]。

结论

有高质量证据表明托吡酯在偏头痛预防中的疗效,但它的使用存在不良事件风险,可能导致治疗中断,从而对患者满意度和对护理的依从性产生负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b00b/10563338/59022d1196f5/10194_2023_1671_Fig1_HTML.jpg

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