Ashkenazi A, Benlifer A, Korenblit J, Silberstein S D
Jefferson Headache Center, Philadelphia, PA 19107, USA.
Cephalalgia. 2006 Oct;26(10):1199-202. doi: 10.1111/j.1468-2982.2006.01191.x.
Zonisamide is a new antiepileptic drug with multiple mechanisms of action and a favourable pharmacokinetic profile. Preliminary data suggest that zonisamide may be effective in migraine prophylaxis. We evaluated the efficacy and tolerability of zonisamide for migraine prophylaxis in refractory patients. We reviewed the charts of adult patients with International Headache Society-defined episodic migraine (EM) or with transformed migraine (TM) according to the Silberstein-Lipton criteria, who had been treated with zonisamide at our out-patient clinic for at least 60 days. Demographic data, zonisamide dosage and duration of treatment were collected and analysed. Headache frequency, attack duration, headache severity and headache-related disability before and after treatment initiation with zonisamide were compared. Thirty-three patients were included in the study (average age 43.9 +/- 8.4 years; 23 (70%) with TM and 10 (30%) with EM). The patients had failed an average of 6.2 migraine prophylactic drugs prior to zonisamide. The average zonisamide daily dose was 337.9 +/- 146.3 mg and the average duration of treatment was 186.4 +/- 174.0 days. The average number of days with headache per month was reduced in the entire study population from 20.7 +/- 9.5 before zonisamide treatment to 18.0 +/- 11.3 after its initiation (P = 0.06) [in TM from 24.7 +/- 7.3 to 21.0 +/- 10.7 (P = 0.06); in EM from 11.6 +/- 7.6 to 11.0 +/- 9.7 (P = NS)]. No significant changes in other headache parameters were found. Fourteen patients (42.4%) reported adverse events (AEs), the most common of which was fatigue. Most patients (12/14, 85.7%) rated AEs as mild or moderate. In this group of refractory migraine patients, zonisamide therapy did not result in a statistically significant beneficial effect on headache or on associated symptoms.
唑尼沙胺是一种具有多种作用机制且药代动力学特征良好的新型抗癫痫药物。初步数据表明,唑尼沙胺可能对偏头痛预防有效。我们评估了唑尼沙胺在难治性患者中预防偏头痛的疗效和耐受性。我们回顾了根据国际头痛协会定义的发作性偏头痛(EM)或根据西尔伯斯坦 - 利普顿标准诊断的转化型偏头痛(TM)成年患者的病历,这些患者在我们门诊接受唑尼沙胺治疗至少60天。收集并分析了人口统计学数据、唑尼沙胺剂量和治疗持续时间。比较了开始使用唑尼沙胺治疗前后的头痛频率、发作持续时间、头痛严重程度和与头痛相关的残疾情况。33例患者纳入研究(平均年龄43.9±8.4岁;23例(70%)为TM,10例(30%)为EM)。患者在使用唑尼沙胺之前平均试用过6.2种偏头痛预防药物。唑尼沙胺平均日剂量为337.9±146.3毫克,平均治疗持续时间为186.4±174.0天。整个研究人群每月头痛天数的平均值从唑尼沙胺治疗前的20.7±9.5天降至治疗开始后的18.0±11.3天(P = 0.06)[TM患者从24.7±7.3天降至21.0±10.7天(P = 0.06);EM患者从11.6±7.6天降至11.0±9.7天(P =无显著性差异)]。未发现其他头痛参数有显著变化。14例患者(42.4%)报告了不良事件(AE),最常见的是疲劳。大多数患者(12/14,85.7%)将不良事件评为轻度或中度。在这组难治性偏头痛患者中,唑尼沙胺治疗对头痛或相关症状未产生统计学上显著的有益效果。