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经前期依来曲普坦预防月经性偏头痛:一项开放标签研究。

Perimenstrual eletriptan prevents menstrual migraine: an open-label study.

机构信息

Department of Anesthesiology & Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

出版信息

Headache. 2010 Apr;50(4):551-62. doi: 10.1111/j.1526-4610.2010.01628.x. Epub 2010 Mar 2.

Abstract

OBJECTIVE

To prospectively evaluate the efficacy of perimenstrual prophylaxis with eletriptan to reduce headaches in women identified with menstrual migraine (MM).

METHODS

Female migraineurs self-reporting a substantial relationship between migraine and menses were evaluated with 3 consecutive months of daily headache recording diaries. A relationship between menses and migraine was evaluated using International Classification of Headache Disorders (ICHD-II) criteria and a probability model called Probability MM. Women prospectively diagnosed with ICHD-II MM were treated for 3 consecutive months with perimenstrual eletriptan 20 mg 3 times daily starting 2 days prior to the expected onset of menstruation and continued for a total of 6 days. Headache activity was compared during the 3 months of recording prior to eletriptan therapy and 3 months with eletriptan perimenstrual prevention therapy.

RESULTS

Three months of pretreatment prospective diaries were completed by 126 women. ICHD-II menstrually related migraine was diagnosed in 74%, with pure MM in 7%. Among those women diagnosed with ICHD-II MM, 61 completed at least 1 treatment month. Overall change in headache activity was a 46% decrease. The mean percentage of treated menses without migraine occurring during the 6 days of treatment was 71%. The percentage of subjects with 1, 2, and 3 migraine-free menstrual periods (no migraines occurring 2 days before menses through the first 3 days of menstruation) with eletriptan, respectively, were 14%, 19%, and 53%. Among those subjects who remained headache-free during the 6 days of eletriptan treatment, migraine occurred during the 3 days immediately after discontinuing eletriptan for 9%. Perimenstrual eletriptan was generally tolerated and no abnormalities were identified on the 6(th) day of treatment using either blood pressure recording or electrocardiogram.

CONCLUSIONS

Among patients with prospectively identified MM, eletriptan 20 mg 3 times daily effectively reduced MM. A significant reduction in headache activity occurred for 53% of patients.

摘要

目的

前瞻性评估经前期预防性应用依来曲普坦治疗月经性偏头痛(MM)女性头痛的疗效。

方法

通过连续 3 个月的每日头痛记录日记,对报告偏头痛与月经存在密切关系的女性偏头痛患者进行评估。使用国际头痛疾病分类(ICHD-II)标准和称为概率 MM 的概率模型评估月经与偏头痛之间的关系。前瞻性诊断为 ICHD-II MM 的女性患者在连续 3 个月中,在预期月经来潮前 2 天开始每天服用依来曲普坦 20mg,每日 3 次,共 6 天。在服用依来曲普坦治疗前的 3 个月和经前期依来曲普坦预防治疗的 3 个月中,比较头痛活动情况。

结果

126 名女性完成了 3 个月的治疗前前瞻性日记。74%的女性被诊断为 ICHD-II 与月经相关的偏头痛,7%的女性为单纯 MM。在被诊断为 ICHD-II MM 的女性中,61 名女性至少完成了 1 个治疗月。头痛活动的总体变化为 46%减少。在治疗的 6 天内,无偏头痛发生的治疗性月经百分比平均为 71%。分别有 14%、19%和 53%的受试者在服用依来曲普坦时,有 1、2 和 3 个无偏头痛的月经周期(从月经来潮前 2 天至月经来潮的前 3 天无偏头痛发作)。在依来曲普坦治疗的 6 天内保持无头痛的受试者中,有 9%的人在停止依来曲普坦后 3 天内发生偏头痛。经前期依来曲普坦一般可耐受,在治疗的第 6 天,使用血压记录或心电图均未发现异常。

结论

在经前瞻性识别的 MM 患者中,依来曲普坦 20mg,每日 3 次,有效减少了 MM。53%的患者头痛活动明显减少。

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