Hemispherotomy for Drug-Resistant Epilepsy in a Low-resource Setting: Surgical Outcomes and Quality of Life in 23 Children Treated in a Hybrid Program in Panama.

IF 1.3 4区 医学 Q4 CLINICAL NEUROLOGY
Emmajane G Rhodenhiser, David Bonda, Carmen Baez, Hannah K Weiss, Yosef Dastagirzada, Guzman Aranda, Laurent Bruggeman, Ameeta Grover, Shaun D Rodgers, Ruben Kuzniecky, Yvonne Zelenka-Kuzniecky, Howard L Weiner, Eveline Teresa Hidalgo
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引用次数: 0

Abstract

Introduction: Hemispherotomy is an effective treatment for children with drug-resistant epilepsy (DRE). While hemispherotomy techniques and indications have evolved, access remains predominantly constrained to high resource settings.

Methods: We performed a retrospective analysis of children who underwent hemispherotomy from 2011 to 2023 by a hybrid team, including local Panamanian and US neurologists, neurosurgeons and EEG technicians and analyzed surgical, epilepsy and quality of life (QoL) parameters. Follow-up data was collected according to the International Consortium for Health Outcomes Measurement (ICHOM) guidelines for children with epilepsy.

Results: Twenty-three children underwent hemispherotomy. The median age at surgery was 10 years (range 2-20). The median follow-up time was six years (range 1-13). The etiology of DRE included malformations of cortical development in 14 children (60.8%), including 8 (34.8%) with schizencephaly, and secondary causes in 9 children (39.1%). Seizure frequency improved for all 23 children (100%): Engel I was achieved in 15 children (65.2%), Engel II (26.1%) in six children, and Engel III (8.7%) in two children. Patients with seizure freedom had significantly fewer preoperative seizures per day than patients with seizure recurrence. Complications occurred in six children (26.1%): 2 wound infections, 2 meningitis, 1 femoral vein thrombosis and 1 wound hematoma with return to OR. There was no perioperative mortality, and no postoperative hydrocephalus or CSF diversion. QoL-related outcomes were available for 16 children: 16/16 (100%) reported that the surgery was a worthwhile and repeatable choice, 14 (87.5%) reported improved cognitive function, the median QOLCE-16 score was 62.5±21.

Conclusion: Hemispherotomy for DRE in select children is a safe and effective surgery in a public children's hospital in a low-resource setting. At last follow-up, the majority of children were seizure-free, and all children had decreased seizure frequency. Families reported improved cognitive function, improved QoL and high satisfaction with their decision to pursue this surgery.

半球切开术治疗低资源环境下的耐药癫痫:在巴拿马一个混合项目中治疗的23名儿童的手术结果和生活质量。
前言:半脑切开术是治疗儿童耐药癫痫的有效方法。虽然半球切开术技术和适应症已经发展,但获取仍然主要局限于高资源环境。方法:我们对2011年至2023年接受半球切除术的儿童进行回顾性分析,由巴拿马和美国当地神经科医生、神经外科医生和脑电图技术人员组成的混合团队,分析手术、癫痫和生活质量(QoL)参数。随访数据是根据国际健康结果测量协会(ICHOM)癫痫儿童指南收集的。结果:23例患儿行半球切开术。手术年龄中位数为10岁(范围2-20岁)。中位随访时间为6年(范围1-13年)。DRE病因包括皮质发育畸形14例(60.8%),其中脑裂畸形8例(34.8%),继发病因9例(39.1%)。23例患儿癫痫发作频率均有改善(100%):15例患儿达到Engel I(65.2%), 6例患儿达到Engel II(26.1%), 2例患儿达到Engel III(8.7%)。发作自由患者术前每日发作次数明显少于发作复发患者。6例患儿(26.1%)出现并发症:伤口感染2例,脑膜炎2例,股静脉血栓形成1例,伤口血肿1例。无围手术期死亡,无术后脑积水或脑脊液分流。16名儿童的生活质量相关结果:16/16(100%)报告手术是值得且可重复的选择,14(87.5%)报告认知功能改善,QOLCE-16中位评分为62.5±21。结论:在资源匮乏的公立儿童医院,半脑切开术是一种安全有效的手术方法。最后随访时,大多数患儿无癫痫发作,所有患儿癫痫发作频率均下降。家庭报告认知功能得到改善,生活质量得到改善,对他们决定进行手术的满意度很高。
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来源期刊
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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