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A randomized trial of levodopa as treatment for residual amblyopia in older children.
Repka, Michael X; Kraker, Raymond T; Dean, Trevano W; Beck, Roy W; Siatkowski, R Michael; Holmes, Jonathan M; Beauchamp, Cynthia L; Golden, Richard P; Miller, Aaron M; Verderber, Lisa C; Wallace, David K.
Afiliação
  • Repka MX; Wilmer Ophthalmological Institute, Johns Hopkins University, Baltimore, Maryland. Electronic address: pedig@jaeb.org.
  • Kraker RT; Jaeb Center for Health Research, PEDIG Coordinating Center, Tampa, Florida.
  • Dean TW; Jaeb Center for Health Research, PEDIG Coordinating Center, Tampa, Florida.
  • Beck RW; Jaeb Center for Health Research, PEDIG Coordinating Center, Tampa, Florida.
  • Siatkowski RM; Dean McGee Eye Institute, University of Oklahoma, Oklahoma City, Oklahoma.
  • Holmes JM; Department of Ophthalmology, Mayo Clinic, Rochester, Minnesota.
  • Beauchamp CL; Pediatric Ophthalmology and Adult Strabismus PA, Dallas, Texas.
  • Golden RP; Department of Ophthalmology, Nationwide Children's Hospital, Columbus, Ohio.
  • Miller AM; Houston Eye Associates, The Woodlands, Texas.
  • Verderber LC; Pediatric Eye Associates, Wilmette, Illinois.
  • Wallace DK; Duke Eye Center, Durham, North Carolina.
Ophthalmology ; 122(5): 874-81, 2015 May.
Article em En | MEDLINE | ID: mdl-25676904
ABSTRACT

OBJECTIVE:

To assess the efficacy and short-term safety of levodopa as adjunctive treatment to patching for amblyopia.

DESIGN:

Randomized, placebo-controlled trial.

PARTICIPANTS:

One hundred thirty-nine children 7 to 12 years of age with residual amblyopia resulting from strabismus, anisometropia, or both combined (visual acuity [VA], 20/50-20/400) after patching.

METHODS:

Sixteen weeks of oral levodopa or placebo administered 3 times daily while patching the fellow eye 2 hours daily. MAIN OUTCOME

MEASURES:

Mean change in best-corrected amblyopic-eye VA at 18 weeks.

RESULTS:

At 18 weeks, amblyopic-eye VA improved from randomization by an average of 5.2 letters in the levodopa group and by 3.8 letters in the placebo group (difference adjusted for baseline VA, +1.4 letters; 1-sided P=0.06; 2-sided 95% confidence interval, -0.4 to 3.3 letters). No serious adverse effects from levodopa were reported during treatment.

CONCLUSIONS:

For children 7 to 12 years of age with residual amblyopia after patching therapy, oral levodopa while continuing to patch 2 hours daily does not produce a clinically or statistically meaningful improvement in VA compared with placebo and patching.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bandagens / Dopaminérgicos / Levodopa / Ambliopia Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Ophthalmology Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bandagens / Dopaminérgicos / Levodopa / Ambliopia Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Child / Female / Humans / Male Idioma: En Revista: Ophthalmology Ano de publicação: 2015 Tipo de documento: Article