Southwest Neurology Audit and Research group (SoNAR), Department of Neurology, Derriford Hospital, Plymouth, PL6 8DH, UK.
Peninsula Medical School, University of Plymouth, Plymouth, UK.
J Headache Pain. 2021 Jan 9;22(1):5. doi: 10.1186/s10194-020-01214-2.
The CGRP antagonists offer a novel therapeutic approach in migraine. Their utility in patients with severe forms of chronic migraine is a subject of particular interest. We present outcomes of 9 months of erenumab treatment in a cohort of patients with difficult-to-control chronic migraine, all of whom had prior unsatisfactory response to onabotulinumtoxinA.
We offered erenumab to 98 patients with a prior unsatisfactory response to onabotulinumtoxinA. Eighty of 98 had trialled greater occipital nerve injections (82%), 32/98 peripheral neurostimulation (33%) and 18/98 intravenous dihydroergotamine (18%). Thirty eight of 98 (39%) met the definition of triptan overuse and 43/98 (44%) analgesic overuse. All patients met the EHF criteria for 'resistant migraine'. Outcome measures (recorded monthly) included days with headache limiting activities of daily living ("red"), not limiting ("amber"), headache free ("green"), and requiring triptans or other analgesics. Quality of life scores - headache impact test 6 (HIT-6), patient health questionnaire 9 (PHQ-9) and pain disability index (PDI) - were also measured.
Mean number of red days improved by - 6.4 days (SE 0.67, 95%CI - 7.7 to - 5.1, p=0.001) at 3 months; - 6.8 days (SE 0.96, 95%CI - 8.80 to - 4.9, p=0.001) at 6 months and - 6.5 days (SE 0.86, 95%CI - 8.3 to - 4.8, p=0.001) at 9 months. Repeated measures ANOVA confirmed improvements in the number of red (p=0.001), green (p=0.001), triptan (p=0.001) and painkiller days (p=0.001) as well as scores of the HIT-6 (p=0.001), PHQ-9 (p=0.001), and PDI (p=0.001) across the duration of study.
We observed improvements in pain, medication use and quality of life in onabotulinumtoxinA-resistant chronic migraine patients following erenumab treatment.
CGRP 拮抗剂为偏头痛提供了一种新的治疗方法。它们在慢性偏头痛严重形式患者中的应用是一个特别关注的问题。我们报告了在 98 名对肉毒杆菌毒素 A 治疗反应不佳的患者中使用依那西普治疗 9 个月的结果,这些患者均曾对肉毒杆菌毒素 A 治疗反应不佳。
我们为 98 名对肉毒杆菌毒素 A 治疗反应不佳的患者提供了依那西普治疗。80/98 名患者接受了更剧烈的枕神经注射(82%)、32/98 名患者接受了外周神经刺激(33%)和 18/98 名患者接受了静脉二氢麦角胺(18%)。38/98 名患者(39%)符合曲坦类药物过度使用的定义,43/98 名患者(44%)符合镇痛药过度使用的定义。所有患者均符合“难治性偏头痛”的 EHF 标准。(记录每月)的结果包括头痛限制日常生活活动的天数(“红色”)、不限制(“琥珀色”)、头痛无(“绿色”)以及需要使用曲坦类药物或其他镇痛药的天数。生活质量评分-头痛影响测试 6 项(HIT-6)、患者健康问卷 9 项(PHQ-9)和疼痛残疾指数(PDI)也进行了测量。
在 3 个月时,红色天数的平均值改善了-6.4 天(SE 0.67,95%CI-7.7 至-5.1,p=0.001);在 6 个月时,改善了-6.8 天(SE 0.96,95%CI-8.80 至-4.9,p=0.001);在 9 个月时,改善了-6.5 天(SE 0.86,95%CI-8.3 至-4.8,p=0.001)。重复测量方差分析证实,红色(p=0.001)、绿色(p=0.001)、曲坦类药物(p=0.001)和止痛药(p=0.001)天数以及 HIT-6(p=0.001)、PHQ-9(p=0.001)和 PDI(p=0.001)评分在研究期间均有改善。
我们观察到在对肉毒杆菌毒素 A 治疗反应不佳的慢性偏头痛患者中,依那西普治疗后疼痛、药物使用和生活质量均有所改善。