Exploring the Efficacy and Safety of Vagus Nerve Stimulation for the Treatment of Epilepsy in Patients With Sturge-Weber Syndrome: A Pilot Study

被引:1
作者
Cheng, Zizhang [1 ]
Sun, Weijin [1 ]
Ma, Kaiqiang [1 ]
Wang, Xiongfei [1 ]
Pan, Junhong [1 ]
Ma, Haowei [1 ]
Peng, Xintao [1 ]
Luan, Guoming [1 ,2 ,3 ]
Guan, Yuguang [1 ,2 ,3 ]
机构
[1] Capital Med Univ, SanBo Brain Hosp, Dept Neurosurg, 50 Xiangshan Yikesong, Beijing 100093, Peoples R China
[2] Beijing Key Lab Epilepsy, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Inst Brain Disorders, Collaborat Innovat Ctr Brain Disorders, Ctr Epilepsy, Beijing, Peoples R China
关键词
Sturge-Weber syndrome (SWS); Vagus nerve stimulation (VNS); Drug-refractory epilepsy; Safety analysis; Treatment efficacy; CHILDREN; AGE;
D O I
10.1016/j.pediatrneurol.2024.12.016
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Sturge-Weber syndrome (SWS) is a rare congenital neurocutaneous disorder, often complicated by epilepsy. Approximately 50% of patients with SWS with epilepsy develop drug-resistant seizures, leaving limited treatment options. Vagus nerve stimulation (VNS) is a known therapy for refractory epilepsy, modulating neural activity to reduce seizures. This study examines the therapeutic outcomes, efficacy, and safety of VNS in five patients with SWS suffering from epilepsy. Methods: A retrospective analysis of VNS treatment data from January 2021 to January 2022 in patients with SWS was conducted. Preoperative assessments included neuroimaging and videoelectroencephalography monitoring. Cognitive function and quality of life were assessed using ageappropriate scales. VNS settings and seizure outcomes were recorded at different follow-up intervals. Seizure outcomes were classified using the modified Engel and McHugh classification. Cognitive function and quality of life were reassessed at two-year follow-up. Results: Five patients, primarily pediatric, with seizure onset between age 0.5 and eight years, were included. After VNS therapy, all patients experienced a reduction in seizure frequency, with one patient becoming seizure free and three achieving a >= 50% reduction in seizures. Two children with cognitive impairments at baseline demonstrated cognitive improvements following treatment. All patients reported significant enhancements in quality of life. VNS was well tolerated, with no major adverse events reported. Conclusions: VNS offers promising therapeutic benefits for epilepsy in patients with SWS, reducing seizure frequency, improving cognitive function in children, and enhancing quality of life with a favorable safety profile. Further research with larger sample sizes and control groups is warranted to validate efficacy and explore personalized treatment options. (c) 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:35 / 40
页数:6
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