Pediatric epilepsy surgery from 2000 to 2018: Changes in referral and surgical volumes, patient characteristics, genetic testing, and postsurgical outcomes

Author:

Eriksson Maria H.1234ORCID,Whitaker Kirstie J.3ORCID,Booth John5ORCID,Piper Rory J.16ORCID,Chari Aswin16ORCID,Martin Sanfilippo Patricia12,Caballero Ana Perez7,Menzies Lara8,McTague Amy14ORCID,Adler Sophie1ORCID,Wagstyl Konrad9ORCID,Tisdall Martin M.16ORCID,Cross J. Helen1410ORCID,Baldeweg Torsten12ORCID

Affiliation:

1. Developmental Neurosciences Research and Teaching Department UCL Great Ormond Street Institute of Child Health London UK

2. Department of Neuropsychology Great Ormond Street Hospital NHS Trust London UK

3. The Alan Turing Institute London UK

4. Department of Neurology Great Ormond Street Hospital NHS Trust London UK

5. Digital Research Environment Great Ormond Street Hospital NHS Trust London UK

6. Department of Neurosurgery Great Ormond Street Hospital NHS Trust London UK

7. North Thames Genomic Laboratory Hub Great Ormond Street Hospital NHS Trust London UK

8. Department of Clinical Genetics Great Ormond Street Hospital NHS Trust London UK

9. Imaging Neuroscience UCL Queen Square Institute of Neurology London UK

10. Young Epilepsy Lingfield UK

Abstract

AbstractObjectiveNeurosurgery is a safe and effective form of treatment for select children with drug‐resistant epilepsy. Still, there is concern that it remains underutilized, and that seizure freedom rates have not improved over time. We investigated referral and surgical practices, patient characteristics, and postoperative outcomes over the past two decades.MethodsWe performed a retrospective cohort study of children referred for epilepsy surgery at a tertiary center between 2000 and 2018. We extracted information from medical records and analyzed temporal trends using regression analyses.ResultsA total of 1443 children were evaluated for surgery. Of these, 859 (402 females) underwent surgical resection or disconnection at a median age of 8.5 years (interquartile range [IQR] = 4.6–13.4). Excluding palliative procedures, 67% of patients were seizure‐free and 15% were on no antiseizure medication (ASM) at 1‐year follow‐up. There was an annual increase in the number of referrals (7%, 95% confidence interval [CI] = 5.3–8.6; p < .001) and surgeries (4% [95% CI = 2.9–5.6], p < .001) over time. Duration of epilepsy and total number of different ASMs trialed from epilepsy onset to surgery were, however, unchanged, and continued to exceed guidelines. Seizure freedom rates were also unchanged overall but showed improvement (odds ratio [OR] 1.09, 95% CI = 1.01–1.18; p = .027) after adjustment for an observed increase in complex cases. Children who underwent surgery more recently were more likely to be off ASMs postoperatively (OR 1.04, 95% CI = 1.01–1.08; p = .013). There was a 17% annual increase (95% CI = 8.4–28.4, p < .001) in children identified to have a genetic cause of epilepsy, which was associated with poor outcome.SignificanceChildren with drug‐resistant epilepsy continue to be put forward for surgery late, despite national and international guidelines urging prompt referral. Seizure freedom rates have improved over the past decades, but only after adjustment for a concurrent increase in complex cases. Finally, genetic testing in epilepsy surgery patients has expanded considerably over time and shows promise in identifying patients in whom surgery is less likely to be successful.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Cited by 8 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3