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氟伐曲坦与其他曲坦类药物治疗复方口服避孕药诱导的月经性偏头痛的急性发作:三项双盲、随机、交叉、多中心研究的汇总分析。

Frovatriptan vs. other triptans for the acute treatment of oral contraceptive-induced menstrual migraine: pooled analysis of three double-blind, randomized, crossover, multicenter studies.

机构信息

Department of Gynecology and Obstetrics, Women's Headache Center, University of Turin, Via Ventimiglia 3, 10126 Turin, Italy.

出版信息

Neurol Sci. 2013 May;34 Suppl 1(Suppl 1):S83-6. doi: 10.1007/s10072-013-1393-x.

DOI:10.1007/s10072-013-1393-x
PMID:23695052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3661071/
Abstract

Oral contraceptive-induced menstrual migraine (OCMM) is a particularly severe form of migraine triggered by the cyclic hormone withdrawal. To review the efficacy of frovatriptan vs. other triptans, in the acute treatment of OCMM through a pooled analysis of three individual randomized Italian studies. With or without aura migraineurs were randomized to frovatriptan 2.5 mg or rizatriptan 10 mg (study 1), frovatriptan 2.5 mg or zolmitriptan 2.5 mg (study 2), frovatriptan 2.5 mg or almotriptan 12.5 mg (study 3). All studies had a multicenter, randomized, double-blind, crossover design. After treating 1-3 episodes of migraine in 3 months with the first treatment, patients switched to the other treatment for the next 3 months. In this analysis, the subset of 35 of the 280 women of the intention-to-treat population taking combined oral contraceptives and experiencing a migraine attack during the withdrawal phase, were analyzed. The proportion of pain free and pain relief at 2 h were 25 and 51 % with frovatriptan and 28 and 48 % with comparators (p = NS). At 24 h, 71 and 83 % of frovatriptan-treated patients and 60 and 76 % of comparator-treated patients were pain free (p < 0.05 between treatments) and had pain relief (p = NS), respectively. Relapse at 24 and 48 h was significantly (p < 0.05) lower with frovatriptan (17 and 21 %) than with the comparators (27 and 31 %). Our results suggest that, due to its sustained antimigraine effect, frovatriptan may be particularly suitable for the management of OCMM than other triptans.

摘要

口服避孕药诱导的经期偏头痛(OCMM)是一种特别严重的偏头痛形式,由周期性激素撤退引发。通过对三项意大利独立随机研究的汇总分析,评估氟伐曲坦与其他曲坦类药物在 OCMM 急性治疗中的疗效。有或无先兆偏头痛患者随机分为氟伐曲坦 2.5mg 或利扎曲坦 10mg(研究 1)、氟伐曲坦 2.5mg 或佐米曲坦 2.5mg(研究 2)、氟伐曲坦 2.5mg 或阿莫曲坦 12.5mg(研究 3)。所有研究均为多中心、随机、双盲、交叉设计。在 3 个月内用第一种治疗方案治疗 1-3 次偏头痛发作后,患者在下 3 个月切换到另一种治疗方案。在本分析中,对意向治疗人群中 280 名服用复方口服避孕药且在撤退期出现偏头痛发作的 35 名女性进行了分析。氟伐曲坦组无疼痛和 2 小时缓解疼痛的比例分别为 25%和 51%,而对照组分别为 28%和 48%(p=NS)。在 24 小时时,氟伐曲坦组 71%和 83%的患者无疼痛,而对照组分别为 60%和 76%(治疗组之间差异有统计学意义,p<0.05),并且缓解疼痛的比例分别为 71%和 83%(p=NS)。氟伐曲坦组在 24 和 48 小时的复发率明显低于对照组(p<0.05),分别为 17%和 21%,而对照组分别为 27%和 31%。我们的结果表明,由于氟伐曲坦具有持续的抗偏头痛作用,因此它可能比其他曲坦类药物更适合 OCMM 的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e7/3661071/acf548cb0bbc/10072_2013_1393_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e7/3661071/ab0bcf40c667/10072_2013_1393_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e7/3661071/acf548cb0bbc/10072_2013_1393_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e7/3661071/ab0bcf40c667/10072_2013_1393_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e7/3661071/acf548cb0bbc/10072_2013_1393_Fig2_HTML.jpg

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本文引用的文献

1
Frovatriptan: a review of its use in the acute treatment of migraine.夫罗曲坦:在偏头痛急性治疗中的应用评价。
CNS Drugs. 2012 Sep 1;26(9):791-811. doi: 10.2165/11209380-000000000-00000.
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The 2012 AHS/AAN guidelines for prevention of episodic migraine: a summary and comparison with other recent clinical practice guidelines.2012 年美国头痛学会/美国神经病学学会偏头痛预防指南:摘要及与其他近期临床实践指南的比较。
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Efficacy of frovatriptan versus other triptans in the acute treatment of menstrual migraine: pooled analysis of three double-blind, randomized, crossover, multicenter studies.
性别与曲普坦类药物疗效:三项双盲、随机、交叉、多中心意大利研究的汇总分析,比较了夫罗曲普坦与其他曲普坦类药物。
Neurol Sci. 2014 May;35 Suppl 1(Suppl 1):99-105. doi: 10.1007/s10072-014-1750-4.
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Neurol Sci. 2012 May;33 Suppl 1(Suppl 1):S65-9. doi: 10.1007/s10072-012-1044-7.
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Italian guidelines for primary headaches: 2012 revised version.意大利原发性头痛指南:2012 年修订版。
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Neurology. 2012 Apr 24;78(17):1337-45. doi: 10.1212/WNL.0b013e3182535d20.
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Gynecol Endocrinol. 2010 Oct;26(10):773-9. doi: 10.3109/09513590.2010.487607.