Binder W J, Brin M F, Blitzer A, Schoenrock L D, Pogoda J M
University of California, USA.
Otolaryngol Head Neck Surg. 2000 Dec;123(6):669-76. doi: 10.1067/mhn.2000.110960.
The object of this clinical experience was to evaluate the correlation between pericranial botulinum toxin type A (BOTOX, Allergan Corp, Irvine, CA) administration and alleviation of migraine headache symptoms.
A nonrandomized, open-label study was performed at 4 different test sites. The subjects consisted of 106 patients, predominantly female, who either (1) initially sought BOTOX treatment for hyperfunctional facial lines or other dystonias with concomitant headache disorders, or (2) were candidates for BOTOX treatment specifically for headaches. Headaches were classified as true migraine, possible migraine, or nonmigraine, based on baseline headache characteristics and International Headache Society criteria. BOTOX was injected into the glabellar, temporal, frontal, and/or suboccipital regions of the head and neck. Main outcome measures were determined by severity and duration of response. The degrees of response were classified as: (1) complete (symptom elimination), (2) partial > or =50% reduction in headache frequency or severity), and (3) no response [neither (1) nor (2)]. Duration of response was measured in months for the prophylactic group.
Among 77 true migraine subjects treated prophylactically, 51% (95% confidence interval, 39% to 62%) reported complete response with a mean (SD) response duration of 4.1 (2.6) months; 38% reported partial response with a mean (SD) response duration of 2.7 (1.2) months. Overall improvement was independent of baseline headache characteristics. Seventy percent (95% confidence interval, 35% to 93%) of 10 true migraine patients treated acutely reported complete response with improvement 1 to 2 hours after treatment. No adverse effects were reported.
BOTOX was found to be a safe and effective therapy for both acute and prophylactic treatment of migraine headaches. Further research is needed to explore and develop the complete potential for the neuroinhibitory effects of botulinum toxin.
本临床经验的目的是评估经颅注射A型肉毒杆菌毒素(保妥适,艾尔建公司,加利福尼亚州欧文市)与偏头痛症状缓解之间的相关性。
在4个不同的试验地点进行了一项非随机、开放标签的研究。受试者包括106名患者,主要为女性,她们要么(1)最初因面部功能亢进性皱纹或其他肌张力障碍伴发头痛障碍而寻求保妥适治疗,要么(2)是专门因头痛而适合保妥适治疗的患者。根据基线头痛特征和国际头痛协会标准,头痛被分类为真性偏头痛、可能偏头痛或非偏头痛。保妥适被注射到头颈部的眉间、颞部、额部和/或枕下区域。主要结局指标由反应的严重程度和持续时间确定。反应程度分为:(1)完全缓解(症状消除),(2)部分缓解(头痛频率或严重程度降低≥50%),以及(3)无反应[既不是(1)也不是(2)]。预防组的反应持续时间以月为单位测量。
在77名接受预防性治疗的真性偏头痛受试者中,51%(95%置信区间,39%至62%)报告完全缓解,平均(标准差)反应持续时间为4.1(2.6)个月;38%报告部分缓解,平均(标准差)反应持续时间为2.7(1.2)个月。总体改善与基线头痛特征无关。10名接受急性治疗的真性偏头痛患者中有70%(95%置信区间,35%至93%)报告完全缓解,治疗后1至2小时症状改善。未报告不良反应。
发现保妥适是一种用于偏头痛急性和预防性治疗的安全有效的疗法。需要进一步研究来探索和开发肉毒杆菌毒素神经抑制作用的全部潜力。