阿仑单抗治疗创伤后头痛-偏头痛表型的观察性研究

J. A. Charles
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引用次数: 8

摘要

目的观察艾仑单抗治疗轻度创伤后头痛-偏头痛伴先兆和不伴先兆的疗效。背景外伤性头痛后偏头痛的药物治疗尚无临床算法。大多数通常使用的偏头痛预防药物要么无效,要么不耐受。方法对7例符合外伤性头痛后有先兆或无先兆偏头痛临床标准,但对常规偏头痛预防药物无效或不耐受的患者,应用阿仑单抗140进行治疗 mg皮下注射。大多数患者没有偏头痛病史。在那些有偏头痛病史的患者中,创伤后头痛偏头痛与过去的偏头痛经历不同。在治疗前后记录使用头部冲击测试-6描述的头痛强度或残疾以及每月头痛天数。所有患者在出现症状时都很虚弱,没有表现出自发消退的迹象。结果患者的应答率为95%(SD 1.22,p < .001)头痛天数减少。所有头部撞击测试-6的分数从致残变为非致残,没有不良反应。大多数患者只需服用一剂erenumab,没有偏头痛复发。疗效的发作通常在几到四周内变得明显。治疗后6个月的延长随访显示没有复发。结论Erenumab在这个小队列中治疗具有偏头痛表型的创伤后头痛是有效的。对于这种没有有效治疗方法的高度流行的致残性疾病,迫切需要进行大规模研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Treatment of posttraumatic headache migraine phenotype with erenumab – An observational study
Objective To report the observed effect of erenumab in mild posttraumatic headache migraine phenotype with and without aura. Background There is no clinical algorithm of pharmacotherapy for migraine following posttraumatic headache. Most migraine preventatives that are typically used are either ineffective or not tolerated. Methods Seven patients who met the clinical criteria for migraine with or without aura following posttraumatic headache who failed or were intolerant of conventional migraine preventatives were treated with erenumab 140 mg subcutaneously. Most had no history of migraine. In those patients with a history of migraine, the posttraumatic headache migraine headaches were different than the past migraine experience. Descriptive headache intensity or disability using the Head Impact Test-6 and monthly headache days were recorded before and after treatment. All patients were debilitated on presentation and demonstrated no signs of spontaneous resolution. Results Patients responded with a 95% (SD 1.22, p < .001) reduction in headache days. All Head Impact Test-6 scores went from disabling to non-disabling without adverse effects. Most required only one dose of erenumab with no migraine recurrence. Onset of efficacy often became apparent within days to four weeks. Extended follow-up six months after treatment revealed no relapses. Conclusions Erenumab is effective in the treatment of posttraumatic headache with migraine phenotype in this small cohort. Large-scale studies are urgently required for this highly prevalent, disabling, condition which has no effective established treatment.
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