Amblyopia treatment outcomes in patients with neurodevelopmental disorders.


Journal

Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
ISSN: 1528-3933
Titre abrégé: J AAPOS
Pays: United States
ID NLM: 9710011

Informations de publication

Date de publication:
10 2023
Historique:
received: 02 03 2023
revised: 21 07 2023
accepted: 22 07 2023
pmc-release: 01 10 2024
medline: 23 10 2023
pubmed: 23 9 2023
entrez: 22 9 2023
Statut: ppublish

Résumé

To compare amblyopia treatment outcomes between patients with neurodevelopmental disorders and their typically developing peers. Of 2,311 patients diagnosed with amblyopia between 2010 and 2014 at Boston Children's Hospital, 460 met inclusion criteria (age 2-12 with anisometropic, strabismic, or mixed amblyopia [interocular difference (IOD) ≥2 lines]). Treatment and visual outcomes were analyzed according to neurodevelopmental status: neurodevelopmental delay (DD) versus typical development (TD). The DD group (n = 54) and TD group (n = 406) were similar in demographics, amblyogenic risk factors, baseline visual measures, prescribed therapy, and adherence (P ≥ 0.10). Between-visit follow-up time was longer for the DD group (0.65 [0.42- 0.97] years) than for the TD group (0.5 [0.36-0.82] years; P = 0.023). IOD improved similarly in each group by the last visit (DD, -0.15 logMAR [-0.31 to -0.02]; TD, -0.2 logMAR [-0.38 to -0.1]; P = 0.09). Each group reached amblyopia resolution by the last visit at similar frequencies (DD, 23/54 [43%]; TD, 211/406 [52%]; P > 0.2). DD diagnosis did not independently influence amblyopia resolution (HR, 0.77; 95% CI, 0.53-1.12; P = 0.17), but each additional month of interval time between follow-up visits reduced the likelihood of resolution by 2.7% (HR, 0.67; 95% CI, 0.51-0.87; P = 0.003). Patients with DD and those with TD responded similarly to amblyopia therapy; however, follow-up intervals were longer in patients with DD and correlated with the likelihood of persistent amblyopia, suggesting that greater efforts at assuring follow-up may benefit patients with DD.

Identifiants

pubmed: 37739211
pii: S1091-8531(23)00195-7
doi: 10.1016/j.jaapos.2023.07.014
pmc: PMC10591796
mid: NIHMS1934005
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

276.e1-276.e8

Subventions

Organisme : NEI NIH HHS
ID : K08 EY030164
Pays : United States

Informations de copyright

Copyright © 2023 American Association for Pediatric Ophthalmology and Strabismus. Published by Elsevier Inc. All rights reserved.

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Auteurs

Ryan N Chinn (RN)

Department of Ophthalmology, Boston Children's Hospital, Boston, Massachusetts.

Carol L Wilkinson (CL)

Harvard Medical School, Boston, Massachusetts; Division of Developmental Medicine, Boston Children's Hospital, Boston, Massachusetts.

Steven J Staffa (SJ)

Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children's Hospital Boston, Massachusetts.

Suzanne M Michalak (SM)

Byers Eye Institute, Stanford University School of Medicine, Palo Alto, California.

Talia N Shoshany (TN)

Harvard Medical School, Boston, Massachusetts; Wills Eye Hospital, Jefferson Medical Center, Philadelphia, Pennsylvania.

Kaila Bishop (K)

Department of Ophthalmology, Boston Children's Hospital, Boston, Massachusetts.

David G Hunter (DG)

Department of Ophthalmology, Boston Children's Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts.

Eric D Gaier (ED)

Department of Ophthalmology, Boston Children's Hospital, Boston, Massachusetts; Harvard Medical School, Boston, Massachusetts; Picower Institute for Learning and Memory, Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, Massachusetts. Electronic address: eric.gaier@childrens.harvard.edu.

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Classifications MeSH