Lenaerts M, Bastings E, Sianard J, Schoenen J
University Department of Neurology, University of Liège, Belgium.
Acta Neurol Belg. 1996 Jun;96(2):126-9.
We performed an open prospective study of the prophylactic efficacy of sodium valproate in 56 patients among which 35 migraineurs, 7 chronic tension-type headache patients and 14 patients with combined headaches. We compared the mean number of headache days per month during a one-month-baseline period without prophylactic treatment and during the last month of a 6-month-treatment course. Among secondary parameters, we assessed headache intensity, adverse experiences and we measured valproate blood levels after one and after six months of treatment. Sixty percent of migraineurs had a 75% or more improvement in the number of headache days under sodium valproate, most of the remaining attacks being less severe. There was no significant improvement in chronic tension-type headache patients and only a mild effect in patients with combined headaches, almost exclusively on the migraine component. Thirty percent of patients reported adverse effects of which none was serious: there were 3 drop-outs. We found a moderate, but statistically significant, correlation between efficacy and blood levels of sodium valproate.
我们对56例患者进行了一项关于丙戊酸钠预防效果的开放性前瞻性研究,其中有35例偏头痛患者、7例慢性紧张型头痛患者和14例混合性头痛患者。我们比较了在无预防性治疗的1个月基线期以及6个月治疗疗程最后1个月期间每月的平均头痛天数。在次要参数方面,我们评估了头痛强度、不良事件,并在治疗1个月和6个月后测量了丙戊酸血药浓度。60%的偏头痛患者在服用丙戊酸钠后头痛天数改善了75%或更多,其余大多数发作的严重程度减轻。慢性紧张型头痛患者没有显著改善,混合性头痛患者仅有轻微效果,几乎只对偏头痛成分有效。30%的患者报告有不良反应,但均不严重:有3例退出研究。我们发现丙戊酸钠的疗效与血药浓度之间存在中度但具有统计学意义的相关性。