Bratbak Daniel Fossum, Nordgård Ståle, Stovner Lars Jacob, Linde Mattias, Dodick David W, Aschehoug Irina, Folvik Mari, Tronvik Erling
1 Department of Neurosurgery, St. Olavs Hospital, Trondheim University Hospital, Norway.
2 Department of Neuroscience, NTNU Norwegian University of Science and Technology, Norway.
Cephalalgia. 2017 Apr;37(4):356-364. doi: 10.1177/0333102416648328. Epub 2016 May 6.
Objective The main objective of this pilot study was to investigate the safety of administering onabotulinumtoxinA towards the sphenopalatine ganglion in 10 patients with intractable chronic migraine with an open, uncontrolled design. We also collected efficacy data to provide an indication as to whether future placebo-controlled studies should be performed. Method In a prospective, open-label, uncontrolled study after one-month baseline, we performed bilateral injections of 25 IU onabotulinumtoxinA (total dose 50 IU) toward the sphenopalatine ganglion in a single outpatient session in 10 patients with intractable migraine with a follow-up of 12 weeks. The primary outcome was adverse events and the main efficacy outcome was frequency of moderate and severe headache days in month 2 post-treatment compared to baseline. Results All 10 patients experienced a total of 25 adverse events. The majority of these were different types of local discomfort in the face and jaw, and none were classified as serious. In an intention-to-treat analysis of the main efficacy outcome, a statistically significant reduction of moderate and severe headache days in baseline versus month 2 was observed (16.3 ± 6.2 days baseline versus 7.6 ± 7.6 days month 2, p = 0.009). Eight out of 10 patients experienced an at least 50% reduction of moderate and severe headache days compared to baseline. Conclusion The result warrants randomised, placebo-controlled studies to establish both safety and efficacy of this potential novel treatment of chronic migraine.
目的 本初步研究的主要目的是采用开放、非对照设计,调查向10例顽固性慢性偏头痛患者的蝶腭神经节注射A型肉毒毒素的安全性。我们还收集了疗效数据,以表明未来是否应开展安慰剂对照研究。方法 在一项前瞻性、开放标签、非对照研究中,在为期1个月的基线期后,我们对10例顽固性偏头痛患者在一次门诊就诊时向蝶腭神经节双侧注射25国际单位A型肉毒毒素(总剂量50国际单位),随访12周。主要结局是不良事件,主要疗效结局是治疗后第2个月与基线相比中度和重度头痛天数的频率。结果 所有10例患者共经历了25次不良事件。其中大多数是面部和下颌不同类型的局部不适,且均未被归类为严重不良事件。在对主要疗效结局的意向性分析中,观察到基线期与第2个月相比中度和重度头痛天数有统计学意义的减少(基线期为16.3±6.2天,第2个月为7.6±7.6天,p = 0.009)。10例患者中有8例与基线相比中度和重度头痛天数减少了至少50%。结论 该结果表明有必要开展随机、安慰剂对照研究,以确定这种潜在的慢性偏头痛新疗法的安全性和疗效。