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月经相关性偏头痛的急性治疗与预防:循证综述

Acute treatment and prevention of menstrually related migraine headache: evidence-based review.

作者信息

Pringsheim Tamara, Davenport William Jeptha, Dodick David

机构信息

Division of Neurology, University of Toronto, Toronto, Canada.

出版信息

Neurology. 2008 Apr 22;70(17):1555-63. doi: 10.1212/01.wnl.0000310638.54698.36.

DOI:10.1212/01.wnl.0000310638.54698.36
PMID:18427072
Abstract

Menstrually related migraine (MRM) headache is common in women and associated with substantial disability. Compared to nonmenstrual migraine, MRM attacks are more severe, longer in duration, and have a poorer response to analgesics. The purpose of this guideline is to provide a systematic review and meta-analysis of the existing therapy trials for MRM and evidence-based recommendations for acute and short-term preventive treatment of MRM headache. Prospective, double-blind, randomized controlled trials of any pharmacologic agent for the symptomatic relief or prevention of MRM headache were included in the guideline. The main outcomes considered were the pain response and pain-free response at 2 hours for acute treatment trials, and the incidence of MRM or the number of days on which MRM attacks occurred for short-term prevention trials. Nineteen trials were included in the analysis. The US Preventive Services Task Force quality criteria were used to assess trial quality and to grade recommendations. Based on the evidence, grade B recommendations can be made for the use of sumatriptan 50 and 100 mg, mefenamic acid 500 mg, and rizatriptan 10 mg for the acute treatment of MRM. For the preventive treatment of MRM, there are grade B recommendations for the perimenstrual use of transcutaneous estrogen 1.5 mg, frovatriptan 2.5 mg twice daily, and naratriptan 1 mg twice daily. Choosing among treatment strategies must be based on clinical considerations.

摘要

月经相关性偏头痛(MRM)头痛在女性中很常见,且会导致严重的功能障碍。与非经期偏头痛相比,MRM发作更为严重,持续时间更长,对镇痛药的反应也更差。本指南的目的是对现有的MRM治疗试验进行系统评价和荟萃分析,并为MRM头痛的急性和短期预防性治疗提供循证推荐。指南纳入了任何用于缓解症状或预防MRM头痛的药物的前瞻性、双盲、随机对照试验。急性治疗试验主要考虑的结局是2小时时的疼痛反应和无痛反应,短期预防试验主要考虑的结局是MRM的发生率或MRM发作的天数。分析纳入了19项试验。采用美国预防服务工作组的质量标准来评估试验质量并对推荐进行分级。基于现有证据,对于MRM的急性治疗,可做出B级推荐,使用50毫克和100毫克的舒马曲坦、500毫克的甲芬那酸以及10毫克的利扎曲坦。对于MRM的预防性治疗,可做出B级推荐,在月经周期使用1.5毫克的经皮雌激素、每日两次2.5毫克的夫罗曲普坦以及每日两次1毫克的那拉曲坦。治疗策略的选择必须基于临床考量。

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