Sarıtaş Ayşegül Şeyma, Çağ Eylül Ceren, Atıcı Berfin Cansel, Gemici Yağmur İnalkaç, Batum Melike, Yılmaz Hikmet, Ak Ayşın Kısabay
Celal Bayar University, Department of Neurology, Manisa 45000, Turkey.
Clin Neurol Neurosurg. 2025 Oct;257:109092. doi: 10.1016/j.clineuro.2025.109092. Epub 2025 Aug 5.
This study aimed to evaluate and compare the effects of isolated greater occipital nerve (GON) blockage, combined GON with supraorbital nerve (SON) blockage and control group on sleep quality, pain severity, anxiety and depression, and health-related quality of life (QoL) in individuals with chronic migraine (CM).
At our clinic, bilateral GON and SON blockage is routinely recommended as a standard treatment for CM patients who either fail to benefit from an effective dose of medical prophylaxis (≥3 months) and discontinue it, or who are unable or unwilling to undergo such treatment. Bilateral application is preferred due to the migratory nature of migraine-type headache localization.Due to the risk/potential of marked tenderness in the forehead region during the procedure or more frequent development of redness and ecchymosis afterward, isolated bilateral GON blockage was performed in patients who did not consent to the SON blockage. Following ethical approval, 80 patients with CM were prospectively assigned to either the GON blockage group (n = 40) or the combined GON and SON blockage group (n = 40). A control group (n = 40) consisting of age- sex- and education- matched healthy individuals was also included. Blockages were performed weekly during the first month and then monthly during the second and third months. All participants completed the Pittsburgh Sleep Quality Index (PSQI), Epworth Sleepiness Scale (ESS), Insomnia Severity Index (ISI), Visual Analog Scale for Sleep Quality (VAS-Sleep), Dysfunctional Beliefs and Attitudes about Sleep Scale (DBAS), Pre-Sleep Arousal Scale (PSAS), Morningness-Eveningness Questionnaire (MEQ), International Restless Legs Syndrome Study Group Rating Scale (IRLSSGS), Visual Analog Scale for Pain (VAS-Pain), Migraine Disability Assessment Scale (MIDAS), Headache Impact Test-6 (HIT-6), Pain Catastrophizing Scale (PCS), Hospital Anxiety and Depression Scale (HADS), Modified Fatigue Impact Scale (MFIS), and the 36-Item Short Form Health Survey (SF-36) at baseline and post-intervention.
In patients who underwent GON blockage, significant improvements were observed in PSQI, ISI, VAS-Sleep, PSAS, VAS-Pain, PCS, MIDAS, HIT-6, HADS, and the SF-36 domains of role limitations-physical, energy/vitality/fatigue, mental health, bodily pain as well as MFIS scores (p < 0.001). Significant improvements compared to baseline were also observed in DBAS, IRLSSGS, and the SF-36 domains of physical functioning, role limitations-emotional, social functioning, physical health, and change in health parameters (p = 0.009, 0.004, 0.002, 0.001, 0.001, 0.005, and 0.001, respectively). In patients who underwent combined GON and SON blockage, significant improvements were observed in ESS, DBAS and the SF-36 domains of physical functioning and role limitations-physical (p = 0.001, 0.031, 0.003, and 0.012, respectively). Additionally, significant improvements compared to baseline were found in PSQI, ISI, VAS-Sleep, PSAS, IRLSSGS, VAS-Pain, PCS, MIDAS, HIT-6, HADS, and the SF-36 domains of role limitations-emotional, energy/vitality/fatigue, mental health, social functioning, bodily pain, physical health, change in health, as well as MFIS scores (p < 0.001). The combined nerve blockages were more effective in enhancing sleep quality, reducing pain and fatigue, and improving psychological well-being and key domains of QoL (p < 0.05).
Despite the short follow-up period, combined GON and SON blockages provided superior clinical outcomes compared with isolated GON blockages, highlighting the therapeutic potential in the management of CM.
本研究旨在评估和比较孤立枕大神经(GON)阻滞、GON联合眶上神经(SON)阻滞及对照组对慢性偏头痛(CM)患者睡眠质量、疼痛严重程度、焦虑和抑郁以及健康相关生活质量(QoL)的影响。
在我们的诊所,对于未能从有效剂量的药物预防(≥3个月)中获益并停药,或无法或不愿接受此类治疗的CM患者,常规推荐双侧GON和SON阻滞作为标准治疗。由于偏头痛型头痛定位具有游走性,故首选双侧应用。由于手术过程中前额区域有明显压痛风险/可能性,或术后更频繁出现发红和瘀斑,对于不同意SON阻滞的患者进行孤立双侧GON阻滞。经伦理批准后,80例CM患者被前瞻性地分为GON阻滞组(n = 40)或GON联合SON阻滞组(n = 40)。还纳入了一个由年龄、性别和教育程度匹配的健康个体组成的对照组(n = 40)。在第一个月每周进行一次阻滞,然后在第二和第三个月每月进行一次。所有参与者在基线和干预后完成匹兹堡睡眠质量指数(PSQI)、爱泼华嗜睡量表(ESS)、失眠严重程度指数(ISI)、睡眠质量视觉模拟量表(VAS-睡眠)、睡眠功能失调信念和态度量表(DBAS)、睡前觉醒量表(PSAS)、晨型-夜型问卷(MEQ)、国际不宁腿综合征研究组评分量表(IRLSSGS)、疼痛视觉模拟量表(VAS-疼痛)、偏头痛残疾评估量表(MIDAS)、头痛影响测试-6(HIT-6)、疼痛灾难化量表(PCS)、医院焦虑抑郁量表(HADS)、改良疲劳影响量表(MFIS)以及36项简短健康调查问卷(SF-36)。
在接受GON阻滞的患者中,观察到PSQI、ISI、VAS-睡眠、PSAS、VAS-疼痛、PCS、MIDAS、HIT-6、HADS以及SF-36中角色限制-身体、精力/活力/疲劳、心理健康、身体疼痛以及MFIS评分等方面有显著改善(p < 0.001)。与基线相比,在DBAS、IRLSSGS以及SF-36中身体功能、角色限制-情感、社会功能、身体健康和健康参数变化等方面也观察到显著改善(分别为p = 0.009、0.004
、0.002、0.001、0.001、0.005和0.001)。在接受GON联合SON阻滞的患者中,观察到ESS、DBAS以及SF-36中身体功能和角色限制-身体方面有显著改善(分别为p = 0.001、0.031、0.003和0.012)。此外,与基线相比,在PSQI、ISI、VAS-睡眠、PSAS、IRLSSGS、VAS-疼痛、PCS、MIDAS、HIT-6、HADS以及SF-36中角色限制-情感、精力/活力/疲劳、心理健康、社会功能、身体疼痛、身体健康、健康变化以及MFIS评分等方面也发现有显著改善(p < 0.001)。联合神经阻滞在提高睡眠质量、减轻疼痛和疲劳以及改善心理健康和QoL关键领域方面更有效(p < 0.05)。
尽管随访期较短,但与孤立GON阻滞相比,GON联合SON阻滞提供了更好的临床结果,突出了其在CM管理中的治疗潜力。