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Refractive Error Change and Overminus Lens Therapy for Childhood Intermittent Exotropia.
Chen, Angela M; Erzurum, S Ayse; Chandler, Danielle L; Hercinovic, Amra; Wu, Rui; Vricella, Marilyn; Waters, Amy L; Ticho, Benjamin H; Erickson, John W; Han, Silvia; McDowell, Paula S; Li, Zhuokai; Kraker, Raymond T; Holmes, Jonathan M; Cotter, Susan A.
Afiliación
  • Chen AM; Southern California College of Optometry at Marshall B. Ketchum University, Fullerton.
  • Erzurum SA; Eye Care Associates, Poland, Ohio.
  • Chandler DL; Jaeb Center for Health Research, Tampa, Florida.
  • Hercinovic A; Jaeb Center for Health Research, Tampa, Florida.
  • Wu R; Jaeb Center for Health Research, Tampa, Florida.
  • Vricella M; State University of New York, College of Optometry, New York.
  • Waters AL; Children's Mercy Hospitals and Clinics, Kansas City, Missouri.
  • Ticho BH; Ticho Eye Associates, Chicago Ridge, Illinois.
  • Erickson JW; Nemours Children's Clinic, Jacksonville, Florida.
  • Han S; Southern California College of Optometry at Marshall B. Ketchum University, Fullerton.
  • McDowell PS; Michigan College of Optometry at Ferris State University, Big Rapids.
  • Li Z; Jaeb Center for Health Research, Tampa, Florida.
  • Kraker RT; Jaeb Center for Health Research, Tampa, Florida.
  • Holmes JM; University of Arizona, Tucson.
  • Cotter SA; Southern California College of Optometry at Marshall B. Ketchum University, Fullerton.
JAMA Ophthalmol ; 142(5): 417-428, 2024 May 01.
Article en En | MEDLINE | ID: mdl-38536764
ABSTRACT
Importance Increased myopic shift was found to be associated with 1 year of overminus spectacle treatment for children with intermittent exotropia (IXT). Persistence of myopic shift after discontinuing overminus spectacles is unknown.

Objective:

To compare refractive error change over 3 years in children with IXT originally treated with overminus vs nonoverminus spectacles. Design, Setting, and

Participants:

This study was an 18-month extension of the Trial of Overminus Spectacle Therapy for Intermittent Exotropia cohort, which previously randomized children aged 3 to 10 years with IXT and baseline spherical equivalent refractive error (SER) between -6.00 diopters (D) and 1.00 D to overminus spectacles (-2.50 D for 12 months, -1.25 D for 3 months, and nonoverminus for 3 months) or nonoverminus spectacles. Children were recruited from 56 sites from July 2010 to February 2022. Data were analyzed from February 2022 to January 2024.

Interventions:

After trial completion at 18 months, participants were followed up at 24 and 36 months. Treatment was at investigator discretion from 18 to 36 months. Main Outcomes and

Measures:

Change in SER (cycloplegic retinoscopy) from baseline to 36 months.

Results:

Of 386 children in the Trial of Overminus Spectacle Therapy for Intermittent Exotropia, 223 (57.8%) consented to 18 months of additional follow-up, including 124 of 196 (63.3%) in the overminus treatment group and 99 of 190 (52.1%) in the nonoverminus treatment group. Of 205 children who completed 36-month follow-up, 116 (56.6%) were female, and the mean (SD) age at randomization was 6.2 (2.1) years. Mean (SD) SER change from baseline to 36 months was greater in the overminus group (-0.74 [1.00] D) compared with the nonoverminus group (-0.44 [0.85] D; adjusted difference, -0.36 D; 95% CI, -0.59 to -0.12; P = .003), with 30 of 112 (26.8%) in the overminus group having more than 1 D of myopic shift compared with 14 of 91 (15%) in the nonoverminus group (risk ratio, 1.8; 95% CI, 1.0-3.0). From 12 to 36 months, mean (SD) myopic shift was -0.34 (0.67) D and -0.36 (0.66) D in the overminus and nonoverminus groups, respectively (adjusted difference, -0.001 D; 95% CI, -0.18 to 0.18; P = .99). Conclusions and Relevance The greater myopic shift observed after 1 year of -2.50-D overminus lens treatment remained at 3 years. Both groups had similar myopic shift during the 2-year period after treatment weaning and cessation. The risk of myopic shift should be discussed with parents when considering overminus lens treatment. Trial Registration ClinicalTrials.gov Identifier NCT02807350.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Refracción Ocular / Agudeza Visual / Exotropía / Anteojos Idioma: En Revista: JAMA Ophthalmol Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Refracción Ocular / Agudeza Visual / Exotropía / Anteojos Idioma: En Revista: JAMA Ophthalmol Año: 2024 Tipo del documento: Article