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Effectiveness of vergence/accommodative therapy for accommodative dysfunction in children with convergence insufficiency.
Chen, Angela M; Roberts, Tawna L; Cotter, Susan A; Kulp, Marjean T; Sinnott, Loraine T; Borsting, Eric J; Tea, Yin C; Jones-Jordan, Lisa A; Hertle, Richard; Mitchell, G Lynn; Eugene Arnold, L; Chase, Christopher; Scheiman, Mitchell M.
Afiliación
  • Chen AM; Southern California College of Optometry, Marshall B Ketchum University, Fullerton, USA.
  • Roberts TL; Department of Ophthalmology, Stanford University School of Medicine, Stanford, USA.
  • Cotter SA; Southern California College of Optometry, Marshall B Ketchum University, Fullerton, USA.
  • Kulp MT; The Ohio State University College of Optometry, Columbus, USA.
  • Sinnott LT; The Ohio State University College of Optometry, Columbus, USA.
  • Borsting EJ; Southern California College of Optometry, Marshall B Ketchum University, Fullerton, USA.
  • Tea YC; Nova Southeastern University, Fort Lauderdale, USA.
  • Jones-Jordan LA; The Ohio State University College of Optometry, Columbus, USA.
  • Hertle R; Akron Children's Hospital, Columbus, USA.
  • Mitchell GL; The Ohio State University College of Optometry, Columbus, USA.
  • Eugene Arnold L; The Ohio State University College of Medicine, Columbus, USA.
  • Chase C; Western University, Pomona, USA.
  • Scheiman MM; Salus University Pennsylvania College of Optometry, Pennsylvania, USA.
Ophthalmic Physiol Opt ; 41(1): 21-32, 2021 01.
Article en En | MEDLINE | ID: mdl-33119180
PURPOSE: To determine the effectiveness of office-based vergence/accommodative therapy for improving accommodative amplitude and accommodative facility in children with symptomatic convergence insufficiency and accommodative dysfunction. METHODS: We report changes in accommodative function following therapy among participants in the Convergence Insufficiency Treatment Trial - Attention and Reading Trial with decreased accommodative amplitude (115 participants in vergence/accommodative therapy; 65 in placebo therapy) or decreased accommodative facility (71 participants in vergence/accommodative therapy; 37 in placebo therapy) at baseline. The primary analysis compared mean change in amplitude and facility between the vergence/accommodative and placebo therapy groups using analyses of variance models after 4, 8, 12 and 16 weeks of treatment. The proportions of participants with normal amplitude and facility at each time point were calculated. The average rate of change in amplitude and facility from baseline to week 4, and from weeks 4 to 16, were determined in the vergence/accommodative therapy group. RESULTS: From baseline to 16 weeks, the mean improvement in amplitude was 8.6 dioptres (D) and 5.2 D in the vergence/accommodative and placebo therapy groups, respectively (mean difference = 3.5 D, 95% confidence interval (CI): 1.5 to 5.5 D; p = 0.01). The mean improvement in facility was 13.5 cycles per minute (cpm) and 7.6 cpm in the vergence/accommodative and placebo therapy groups, respectively (mean difference = 5.8 cpm, 95% CI: 3.8 to 7.9 cpm; p < 0.0001). Significantly greater proportions of participants treated with vergence/accommodative therapy achieved a normal amplitude (69% vs. 32%, difference = 37%, 95% CI: 22 to 51%; p < 0.0001) and facility (85% vs. 49%, difference = 36%, 95% CI: 18 to 55%; p < 0.0001) than those who received placebo therapy. In the vergence/accommodative therapy group, amplitude increased at an average rate of 1.5 D per week during the first 4 weeks (p < 0.0001), then slowed to 0.2 D per week (p = 0.002) from weeks 4 to 16. Similarly, facility increased at an average rate of 1.5 cpm per week during the first 4 weeks (p < 0.0001), then slowed to 0.6 cpm per week from weeks 4 to 16 (p < 0.0001). CONCLUSION: Office-based vergence/accommodative therapy is effective for improving accommodative function in children with symptomatic convergence insufficiency and coexisting accommodative dysfunction.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastornos de la Motilidad Ocular / Anteojos Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Ophthalmic Physiol Opt Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastornos de la Motilidad Ocular / Anteojos Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: Ophthalmic Physiol Opt Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos