Suppr超能文献

文拉法辛预防偏头痛的疗效与安全性。

The efficacy and safety of venlafaxine in the prophylaxis of migraine.

作者信息

Ozyalcin Suleyman N, Talu Gul Koknel, Kiziltan Emre, Yucel Basak, Ertas Mustafa, Disci Rian

机构信息

Department of Algology, Istanbul, Turkey.

出版信息

Headache. 2005 Feb;45(2):144-52. doi: 10.1111/j.1526-4610.2005.05029.x.

Abstract

OBJECTIVE

To evaluate the efficacy and safety of venlafaxine in the prophylaxis of migraine.

BACKGROUND

The efficacy of venlafaxine, which is selectively effective on the serotonergic and noradrenergic mechanisms, on various headaches and chronic pain syndromes has been demonstrated. To our knowledge, this is the first placebo-controlled, double-blind, randomized study of two different doses of venlafaxine for migraine treatment.

METHODS

In this prospective study, 60 migraine patients without aura were randomly assigned to venlafaxine XR 75 mg, venlafaxine XR 150 mg, or placebo. The frequency of headache attacks, the severity and the duration of attacks, and analgesic use were monitored every 2 weeks for 2 months. Adverse events and patient satisfaction were also evaluated during these visits. At the end of the 2 months, global efficacy and tolerance were investigated.

RESULTS

A significant difference was observed between the venlafaxine 150 mg and placebo groups in the number of headache attacks (P= .006). According to patient satisfaction comparisons, the active drug groups were significantly different when compared with placebo (P= .001 at visit 2 and visit 6). When the global efficacy was considered, 80% of patients in the 75-mg group and 88.2% of the patients in the 150-mg group evaluated treatment benefits as either good or very good.

CONCLUSIONS

Venlafaxine was more effective than placebo and is safe and well tolerated as migraine prophylaxis.

摘要

目的

评估文拉法辛预防偏头痛的疗效和安全性。

背景

文拉法辛对5-羟色胺能和去甲肾上腺素能机制具有选择性作用,其对各种头痛和慢性疼痛综合征的疗效已得到证实。据我们所知,这是第一项针对两种不同剂量文拉法辛治疗偏头痛的安慰剂对照、双盲、随机研究。

方法

在这项前瞻性研究中,60名无先兆偏头痛患者被随机分配至文拉法辛缓释片75毫克组、文拉法辛缓释片150毫克组或安慰剂组。每2周监测一次头痛发作频率、发作的严重程度和持续时间以及止痛药物的使用情况,持续2个月。在这些访视期间还评估了不良事件和患者满意度。在2个月末,调查总体疗效和耐受性。

结果

文拉法辛150毫克组与安慰剂组在头痛发作次数上存在显著差异(P = 0.006)。根据患者满意度比较,与安慰剂相比,活性药物组存在显著差异(第2次和第6次访视时P = 0.001)。在考虑总体疗效时,75毫克组80%的患者和150毫克组88.2%的患者将治疗效果评为良好或非常好。

结论

文拉法辛预防偏头痛的效果优于安慰剂,且安全并耐受性良好。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验