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偏头痛患者静脉注射丙戊酸盐(奥立菲)和地塞米松的随机临床试验。

Randomized clinical trial of intravenous valproate (orifil) and dexamethasone in patients with migraine disorder.

作者信息

Foroughipour Mohsen, Ghandehari Kavian, Khazaei Mojtaba, Ahmadi Fahimeh, Shariatinezhad Keyvan, Ghandehari Kosar

机构信息

Department of Neurology, Mashhad University of Medical Sciences, Mashhad, Iran;

出版信息

Iran J Med Sci. 2013 Jun;38(2 Suppl):150-5.

Abstract

BACKGROUND

Intravenous Valproate (IVVP) has been used in the treatment of migraine in some studies; however, it is far better known in the management of status epilepticus.

METHODS

Consecutive patients with migraine in our Headache Clinic were enrolled in this prospective, randomized clinical trial in 2011. The patients were randomized into two therapeutic groups, one receiving 900 mg IVVP (Orifil) and the other 16 mg IV Dexamethasone (IVDEX) diluted in 150 CC normal saline and infused for 10 minutes. Worst severity of pain before treatment and least severity at 3 hours after the infusion using a 0-10 point numeric rating scale were recorded. An interview with the patient was performed 72 hours after treatment to detect a possible relapse of headache.

RESULTS

Thirty-one migraine status patients, comprising 28 women and 3 men at a mean±SD age of 33.355±12.373 SD, were investigated. Differences in the therapeutic effects of IVVP (Orifil) and IVDEX on pain score were not significant between the two groups (t=0.933, df=29; P=0.358). Relapse of headache occurred in 68.42% of the IVVP (Orifil) group and 66.67% of the IVDEX group. Distribution of relapse was not significantly different between the two therapeutic groups of patients (P=0.870).

CONCLUSION

IVVP (Orifil) was similar in efficacy to IVDEX as abortive therapy in patients with migraine status. IVVP (Orifil) appears to offer a safe and well-tolerated abortive treatment.

TRIAL REGISTRATION NUMBER

IRCT13891146234N2.

摘要

背景

在一些研究中,静脉注射丙戊酸盐(IVVP)已被用于治疗偏头痛;然而,它在癫痫持续状态的管理中更为人所知。

方法

2011年,我们头痛门诊的连续偏头痛患者被纳入这项前瞻性随机临床试验。患者被随机分为两个治疗组,一组接受900毫克IVVP(奥立菲),另一组接受16毫克静脉注射地塞米松(IVDEX),稀释于150毫升生理盐水中,输注10分钟。记录治疗前疼痛的最严重程度以及输注后3小时使用0至10分数字评分量表的最轻严重程度。治疗72小时后对患者进行访谈,以检测头痛是否可能复发。

结果

对31例偏头痛状态患者进行了调查,其中包括28名女性和3名男性,平均年龄±标准差为33.355±12.373标准差。IVVP(奥立菲)和IVDEX对疼痛评分的治疗效果在两组之间无显著差异(t = 0.933,自由度 = 29;P = 0.358)。IVVP(奥立菲)组68.42%的患者和IVDEX组66.67%的患者出现头痛复发。两组治疗患者的复发分布无显著差异(P = 0.870)。

结论

在偏头痛状态患者中,IVVP(奥立菲)作为中止治疗的疗效与IVDEX相似。IVVP(奥立菲)似乎提供了一种安全且耐受性良好的中止治疗方法。

试验注册号

IRCT13891146234N2。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a617/3771216/f2a6c1be48b2/ijms-38-150-g001.jpg

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