Evidence map›Paper›PMID 40834340›Full record

ArticleNeurology2025

Ultra-High Field 7T MRI in a Drug-Resistant Pediatric Epilepsy Cohort: Image Comparison and Radiologic Outcomes.

Katy Vecchiato, Chiara Casella, Ayse Sila Dokumaci, Ata Siddiqui, Alexia Egloff, Olivia Carney, Jon O Cleary, Jozef Jarosz, Pierluigi Di Ciò, Michela Cleri and 16 more

Abstract readComparative StudyMulticenter Study
In one paragraph

Article in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
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

26 authors.

Katy VecchiatoDepartment for Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.ORCID 0000-0002-7493-5891
Chiara CasellaDepartment for Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.ORCID 0000-0002-0292-3330
Ayse Sila DokumaciLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0001-9035-5689
Ata SiddiquiDepartment of Radiology, Guy's and St. Thomas' NHS Foundation Trust, London, United Kingdom.ORCID 0000-0002-1820-9705
Alexia EgloffResearch Department of Early Life Imaging, School of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0002-2005-8328
Olivia CarneyResearch Department of Early Life Imaging, School of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0002-7900-6776
Jon O ClearySchool of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0001-8836-9934
Jozef JaroszDepartment of Neuroradiology, King's College Hospital NHS Foundation Trust, London, United Kingdom.ORCID 0009-0004-1720-1586
Pierluigi Di CiòLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0002-0457-9449
Michela CleriLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0009-0009-3424-6504
Kathleen ColfordResearch Department of Early Life Imaging, School of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0001-6501-8867
Rory J PiperLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0002-6422-5853
Tomoki ArichiResearch Department of Early Life Imaging, School of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0002-3550-1644
Michael EyreSchool of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0002-6704-5727
Fraser AitkenLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0001-9125-7327
Raphael Tomi-TricotLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0002-6149-9154
Thomas WilkinsonLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0002-7915-2888
Joseph V HajnalLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0002-2690-5495
Colm J McGinnityKing's College London & Guy's and St Thomas' PET Centre, School of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0002-2692-918X
Siti N YaakubSchool of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0001-5084-1973
Sharon L GilesLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0002-8528-3745
Shaihan MalikLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0001-8925-9032
Alexander HammersKing's College London & Guy's and St Thomas' PET Centre, School of Biomedical Engineering and Imaging Sciences, King's College London, United Kingdom.ORCID 0000-0001-9530-4848
Philippa BridgenLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0009-0008-8051-8139
David W CarmichaelLondon Collaborative Ultra high field System (LoCUS), St Thomas' Hospital, United Kingdom.ORCID 0000-0001-9972-0718
Jonathan O'MuircheartaighDepartment for Forensic and Neurodevelopmental Sciences, Institute of Psychiatry, Psychology and Neuroscience, King's College London, United Kingdom.ORCID 0000-0002-8033-6959

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesEpileptogenic lesions in focal epilepsy can be subtle or remain undetected on conventional MRI. Ultra-high field (7T) MRI offers higher spatial resolution, contrast, and signal-to-noise ratio compared with conventional field strengths and has shown promise in adult presurgical evaluation. However, its utility in pediatric focal epilepsy, where malformations of cortical development are common, remains unclear. In this study, we directly compared 7T and 3T MRI in children with drug-resistant focal epilepsy, evaluating (1) scan tolerability, (2) image quality, and (3) lesion detection yield.

methodsIn this prospective cohort study, patients were recruited from outpatient clinics at 3 large epilepsy centers in London. Eligible participants were aged 8-17 years and had no contraindications to MRI. Scanning was conducted in 2 separate sessions at 3T and 7T. Safety and tolerability were assessed using age-specific questionnaires and analyzed using the Mann-Whitney test for differences between age groups and the McNemar χ

resultsA total of 63 children were assessed: 41 patients (mean age 12.6 ± 2.4 years, 22 were male) and 22 healthy controls (8-17 years, mean age 11.7 ± 2.7 years, 15 were male). Both field strengths were well tolerated, and side effects were transient. These included higher dizziness-related discomfort at 7T ( DISCUSSION: 7T MRI in children with epilepsy is well tolerated and associated with a 23% improvement in lesion detection, directly affecting clinical management and surgical outcomes. Although limited by a preselected cohort with extensive diagnostic workups, our findings underscore the transformative potential of 7T MRI in presurgical planning for pediatric epilepsy.

Indexed as

BrainDrug Resistant EpilepsyEpilepsies, PartialMagnetic Resonance ImagingAdolescentChildCohort StudiesFemaleHumansMaleProspective Studies

Identifiers

PMID40834340
PMCPMC12367418

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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.