University of Louisville School of Medicine, Louisville KY 40202, United States.
Division of Child Neurology, Department of Neurology, University of Louisville School of Medicine, Louisville Kentucky 40202, United States.
Seizure. 2024 Apr;117:60-66. doi: 10.1016/j.seizure.2024.01.019. Epub 2024 Feb 2.
Around 11% of patients with absence epilepsy develop drug-resistant absence epilepsy (DRAE), and are at increased risk for developing psychiatric and neurologic comorbidities. Current therapeutic options for DRAE are limited. The purpose of this study was to assess the efficacy of vagus nerve stimulation (VNS) in treating DRAE.
Our institution maintains a database of patients who received VNS between 2010 and 2022. We identified DRAE patients who were <18 years of age at seizure onset, were electro-clinically diagnosed with an absence epilepsy syndrome (childhood absence, juvenile absence, or Jeavons Syndrome) by an epileptologist, and had normal brain imaging. The primary outcome measure was post-VNS absence seizure frequency.
Twenty-six patients (M/F:14/12) were identified. Median age at seizure onset was 7 years (IQR 4-10) and patients experienced seizures for 6 years (IQR 4.3-7.6) before VNS. After VNS, the median absence seizure frequency reduced to 1.5 days (IQR 0.1-3.5) per week from 7 days (IQR 7-7), a 66% reduction seizure frequency. VNS responder rate was 80%, and seven patients achieved seizure freedom. There was no significant effect on VNS efficacy between the time from DRAE diagnosis to VNS placement (p = 0.067) nor the time from first seizure onset to VNS implant (p = 0.80). The median follow-up duration was 4.1 years (IQR 2.4-6.7), without any significant association between follow-up duration and VNS efficacy (r=0.023) CONCLUSIONS: VNS is effective in managing DRAE. The responder rate was 80%; seizure improvement was independent of age at both seizure onset and latency to VNS after meeting DRAE criteria.
约 11%的失神癫痫患者发展为耐药性失神癫痫(DRAE),并且发生精神和神经合并症的风险增加。目前 DRAE 的治疗选择有限。本研究旨在评估迷走神经刺激(VNS)治疗 DRAE 的疗效。
我们的机构维护着一个数据库,其中包含 2010 年至 2022 年间接受 VNS 的患者。我们确定了在癫痫发作时年龄<18 岁、由癫痫专家通过电临床诊断为失神癫痫综合征(儿童失神、青少年失神或 Jeavons 综合征)且脑成像正常的 DRAE 患者。主要观察指标是 VNS 后失神发作频率。
共确定了 26 名患者(男/女:14/12)。癫痫发作的中位年龄为 7 岁(IQR 4-10),患者在 VNS 前经历了 6 年(IQR 4.3-7.6)的癫痫发作。VNS 后,失神发作频率从 7 天(IQR 7-7)的中位 7 天(IQR 0.1-3.5)降低了 66%。VNS 有效率为 80%,7 名患者达到无发作。从 DRAE 诊断到 VNS 放置的时间(p=0.067)或从首次癫痫发作到 VNS 植入的时间(p=0.80)对 VNS 疗效均无显著影响。中位随访时间为 4.1 年(IQR 2.4-6.7),随访时间与 VNS 疗效之间无显著相关性(r=0.023)。
VNS 对 DRAE 有效。有效率为 80%;癫痫发作改善与 DRAE 标准后的癫痫发作起始年龄和 VNS 潜伏期无关。