Department of Neurosurgery, HMU Health and Medical University Potsdam, Ernst von Bergmann Hospital, Potsdam, Germany.
Department of Neurosurgery, University of Jordan, Amman, Jordan.
World Neurosurg. 2021 Jul;151:e472-e483. doi: 10.1016/j.wneu.2021.04.070. Epub 2021 Apr 24.
We have provided long-term data on clinically meaningful pain alleviation for drug-refractory headache disorders using occipital (ONS) and supraorbital nerve stimulation (SONS).
We performed a retrospective review of 96 patients with migraine, cervicogenic headache, cluster headache, neuropathic pain of the scalp, tension-type headache, and new daily persistent headache who had undergone ONS (61.5%), SONS (11.5%), or combined ONS plus SONS (27.1%) trial implantation and definitive implantation from 2007 to 2017. Changes in pain perception over time were monitored using the visual analog scale (VAS) for pain.
The cohort consisted of 60.4% women and 39.6% men, with a mean age of 46.9 ± 11.5 years and pain duration of 14 ± 14.1 years. Of the 96 patients, 65 (67.7%) were treatment responders to a trial (≥30% amelioration in the average or maximum VAS score for pain and/or number of headache days) that had lasted 22.5 ± 8.8 days. The reduction in their average VAS score for pain was to 37% ± 24.4% of baseline compared with 99.1% ± 24.1% of baseline for those without a response (P < 0.01). Of the 56 patients who had undergone implantation and had long-term follow-up data available for ≤10 years, 32 (57.1%) reported a ≥50% reduction in their average VAS score for pain. Four patients (6.5%) had requested hardware explantation. Stage II complications included 1 infection (1.6%) and 6 electrode dislocations (9.7%). The study limitations included the retrospective nature, lack of controls receiving placebo intervention, and randomization.
After careful patient selection according to a positive response to a trial of ONS and/or SONS, clinically meaningful long-term benefit was achieved in 57.1% of our patients with various chronic headache conditions.
我们提供了使用枕神经(ONS)和眶上神经刺激(SONS)治疗药物难治性头痛障碍的长期临床有意义的疼痛缓解数据。
我们对 2007 年至 2017 年间接受 ONS(61.5%)、SONS(11.5%)或 ONS 加 SONS 联合植入(27.1%)试验和确定性植入的 96 例偏头痛、颈源性头痛、丛集性头痛、头皮神经性疼痛、紧张型头痛和新的每日持续性头痛患者进行了回顾性分析。使用视觉模拟评分(VAS)监测疼痛随时间的变化来监测疼痛感知的变化。
该队列包括 60.4%的女性和 39.6%的男性,平均年龄为 46.9±11.5 岁,疼痛持续时间为 14±14.1 年。在 96 例患者中,65 例(67.7%)对试验有治疗反应(平均或最大 VAS 评分疼痛和/或头痛天数改善≥30%),持续时间为 22.5±8.8 天。与无反应者(99.1%±24.1%)相比,他们的平均 VAS 疼痛评分降低至基线的 37%±24.4%(P<0.01)。在 56 例接受植入并可获得长达 10 年的长期随访数据的患者中,32 例(57.1%)报告其平均 VAS 疼痛评分降低≥50%。4 例患者(6.5%)要求取出硬件。二期并发症包括 1 例感染(1.6%)和 6 例电极脱位(9.7%)。研究的局限性包括回顾性、缺乏接受安慰剂干预的对照和随机化。
根据 ONS 和/或 SONS 试验的阳性反应对患者进行仔细选择后,我们的各种慢性头痛患者中有 57.1%获得了长期的临床有意义的益处。