Electrophysiological and fundoscopic detection of intracranial hypertension in craniosynostosis.


Journal

Eye (London, England)
ISSN: 1476-5454
Titre abrégé: Eye (Lond)
Pays: England
ID NLM: 8703986

Informations de publication

Date de publication:
01 2023
Historique:
received: 24 02 2021
accepted: 02 11 2021
revised: 08 10 2021
pubmed: 3 1 2022
medline: 12 1 2023
entrez: 2 1 2022
Statut: ppublish

Résumé

To assess the diagnostic accuracy of fundoscopy and visual evoked potentials (VEPs) in detecting intracranial hypertension (IH) in patients with craniosynostosis undergoing spring-assisted posterior vault expansion (sPVE). Children with craniosynostosis undergoing sPVE and 48-hour intracranial pressure (ICP) monitoring were included in this single-centre, retrospective, diagnostic accuracy study. Data for ICP, fundoscopy and VEPs were analysed. Primary outcome measures were papilloedema on fundoscopy, VEP assessments and IH, defined as mean ICP > 20 mmHg. Diagnostic indices were calculated for fundoscopy and VEPs against IH. Secondary outcome measures included final visual outcomes. Fundoscopic examinations were available for 35 children and isolated VEPs for 30 children, 22 of whom had at least three serial VEPs. Sensitivity was 32.1% for fundoscopy (95% confidence intervals [CI]: 15.9-52.4) and 58.3% for isolated VEPs (95% CI 36.6-77.9). Specificity for IH was 100% for fundoscopy (95% CI: 59.0-100) and 83.3% for isolated VEPs (95% CI: 35.9-99.6). Where longitudinal deterioration was suspected from some prVEPs but not corroborated by all, sensitivity increased to 70.6% (95% CI: 44.0-89.7), while specificity decreased to 60% (95% CI: 14.7-94.7). Where longitudinal deterioration was clinically significant, sensitivity decreased to 47.1% (23.0-72.2) and specificity increased to 100% (47.8-100). Median final BCVA was 0.24 logMAR (n = 36). UK driving standard BCVA was achieved by 26 patients (72.2%), defined as ≥0.30 logMAR in the better eye. Papilloedema present on fundoscopy reliably indicated IH, but its absence did not exclude IH. VEP testing boosted sensitivity at the expense of specificity, depending on method of analysis.

Identifiants

pubmed: 34974540
doi: 10.1038/s41433-021-01839-w
pii: 10.1038/s41433-021-01839-w
pmc: PMC9829653
mid: EMS137959
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

139-145

Subventions

Organisme : DH | National Institute for Health Research (NIHR)
ID : NIHR 300155 Doctoral Fellowship Award

Informations de copyright

© 2021. The Author(s).

Références

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Auteurs

Sohaib R Rufai (SR)

Clinical and Academic Department of Ophthalmology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.
The University of Leicester Ulverscroft Eye Unit, Leicester Royal Infirmary, Robert Kilpatrick Clinical Sciences Building, PO Box 65, Leicester, LE2 7LX, UK.
Craniofacial Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

Oliver R Marmoy (OR)

Clinical and Academic Department of Ophthalmology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.

Dorothy A Thompson (DA)

Clinical and Academic Department of Ophthalmology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.

Lara S van de Lande (LS)

UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.
Craniofacial Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

R William Breakey (RW)

UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.
Craniofacial Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

Catey Bunce (C)

Clinical Trials Unit, The Royal Marsden NHS Foundation Trust, London, SW3 6JJ, UK.

Vasiliki Panteli (V)

Clinical and Academic Department of Ophthalmology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

Kemmy Schwiebert (K)

Clinical and Academic Department of Ophthalmology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

Shafquet Mohamed (S)

Clinical and Academic Department of Ophthalmology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

Frank A Proudlock (FA)

The University of Leicester Ulverscroft Eye Unit, Leicester Royal Infirmary, Robert Kilpatrick Clinical Sciences Building, PO Box 65, Leicester, LE2 7LX, UK.

Irene Gottlob (I)

The University of Leicester Ulverscroft Eye Unit, Leicester Royal Infirmary, Robert Kilpatrick Clinical Sciences Building, PO Box 65, Leicester, LE2 7LX, UK.

David J Dunaway (DJ)

UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.
Craniofacial Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

Richard Hayward (R)

UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.
Craniofacial Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.

Richard Bowman (R)

Clinical and Academic Department of Ophthalmology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.

Noor Ul Owase Jeelani (NUO)

UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK. Owase.Jeelani@gosh.nhs.uk.
Craniofacial Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK. Owase.Jeelani@gosh.nhs.uk.

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