Tomlinson Samuel B, Galligan Kathleen, Kessler Sudha K, Kennedy Benjamin C
Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, 3400 Civic Center Blvd, Philadelphia, PA, 19104, USA.
Division of Neurosurgery, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Childs Nerv Syst. 2025 Apr 25;41(1):168. doi: 10.1007/s00381-025-06825-1.
Hemispherotomy is an effective treatment for well-selected patients with drug-resistant hemispheric epilepsy. Successful hemispherotomy leading to seizure cessation has been associated with improved neurodevelopmental outcomes and reduced healthcare utilization. This study reports seizure outcomes and complications in a large, consecutive, single-surgeon series of pediatric hemispherotomy cases using a surgical approach with modifications to previously-reported techniques.
All patients undergoing transsylvian peri-insular hemispherotomy for drug-resistant hemispheric epilepsy between May 2017 and April 2021 by a single surgeon were prospectively enrolled in an epilepsy surgery registry. With retrospective review of medical records, data were collected on baseline characteristics (demographics, epilepsy history, anti-seizure medications, neurodevelopmental status, EEG features, and imaging characteristics), operative complications, hospital course, and seizure outcomes (Engel scale at 12- and 24-month follow-up).
All 32 consecutive patients (aged 15 months-19 years) were seizure-free (Engel Class 1) 12 and 24 months after hemispherotomy. At 12 months, 31 patients (97%) had Engel Class 1A outcomes, and 1 patient (3%) had an Engel Class 1D outcome. These results were maintained through 24-month follow-up. Among 31 patients taking anti-seizure medications before surgery, 22 (71%) were weaned off all agents by 24 months. One patient (3%) developed post-operative hydrocephalus requiring ventriculoperitoneal shunt placement.
In an etiologically heterogeneous cohort of patients undergoing hemispherotomy for drug-resistant epilepsy, a modified transsylvian peri-insular technique led to high rates of sustained seizure freedom with minimal complications.
大脑半球切除术是治疗精心挑选的耐药性半球癫痫患者的有效方法。成功的大脑半球切除术导致癫痫发作停止与改善神经发育结果和减少医疗资源利用有关。本研究报告了一系列大型、连续、由单一外科医生进行的小儿大脑半球切除术病例的癫痫发作结果和并发症,该手术方法对先前报道的技术进行了改进。
2017年5月至2021年4月期间,由单一外科医生对所有因耐药性半球癫痫接受经外侧裂岛周大脑半球切除术的患者进行前瞻性登记,纳入癫痫手术登记系统。通过回顾病历,收集了患者的基线特征(人口统计学、癫痫病史、抗癫痫药物、神经发育状况、脑电图特征和影像学特征)、手术并发症、住院过程和癫痫发作结果(12个月和24个月随访时的恩格尔分级)。
所有32例连续患者(年龄15个月至19岁)在大脑半球切除术后12个月和24个月均无癫痫发作(恩格尔分级1级)。在12个月时,31例患者(97%)达到恩格尔1A级结果,1例患者(3%)达到恩格尔1D级结果。这些结果在24个月的随访中保持稳定。在术前服用抗癫痫药物的31例患者中,22例(71%)在24个月时停用了所有药物。1例患者(3%)发生术后脑积水,需要进行脑室腹腔分流术。
在因耐药性癫痫接受大脑半球切除术的病因异质性患者队列中,改良的经外侧裂岛周技术导致高比例的持续无癫痫发作,且并发症极少。