Evidence map›Paper›PMID 37264783›Full record

ArticleEpilepsia2023

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

Maria H Eriksson, Kirstie J Whitaker, John Booth, Rory J Piper, Aswin Chari, Patricia Martin Sanfilippo, Ana Perez Caballero, Lara Menzies, Amy McTague, Sophie Adler and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Epilepsia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
8.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  7. AI in epilepsy neuroimaging.Current opinion in neurology · 2026
    Review
  8. Understanding and overcoming delays to pediatric epilepsy surgery: a scoping review.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
    Article
  9. Article
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  14. Observational
  15. Article
  16. Observational
  17. Long-term trends in total administered radiation dose from brain [European journal of nuclear medicine and molecular imaging · 2025
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Maria H ErikssonDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0001-6869-5804
Kirstie J WhitakerThe Alan Turing Institute, London, UK.ORCID 0000-0001-8498-4059
John BoothDigital Research Environment, Great Ormond Street Hospital NHS Trust, London, UK.ORCID 0000-0003-4357-1324
Rory J PiperDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0002-6422-5853
Aswin ChariDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0003-0053-147X
Patricia Martin SanfilippoDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.
Ana Perez CaballeroNorth Thames Genomic Laboratory Hub, Great Ormond Street Hospital NHS Trust, London, UK.
Lara MenziesDepartment of Clinical Genetics, Great Ormond Street Hospital NHS Trust, London, UK.
Amy McTagueDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0002-0334-2909
Sophie AdlerDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0002-3978-7424
Konrad WagstylImaging Neuroscience, UCL Queen Square Institute of Neurology, London, UK.ORCID 0000-0003-3439-5808
Martin M TisdallDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0001-8880-8386
J Helen CrossDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0001-7345-4829
Torsten BaldewegDevelopmental Neurosciences Research and Teaching Department, UCL Great Ormond Street Institute of Child Health, London, UK.ORCID 0000-0002-5724-1679
Great Ormond Street Hospital · GBQueen Mary University of London · GBThe Alan Turing Institute · GB

Funding

Medical Research Council MR/T007087/1Wellcome Trust 215901Wellcome Trust 215 901/Z/19/Z
6 · The paper itself

Abstract

objectiveNeurosurgery 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. SIGNIFICANCE: Children 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.

Indexed as

Drug Resistant EpilepsyEpilepsyChildFemaleGenetic TestingHumansRetrospective StudiesTreatment Outcomeantiseizure medicationepilepsy surgeryoutcomepediatrictrends

Identifiers

PMID37264783
PMCPMC7615891
OpenAlexW4379094792

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.