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One-year follow-up of clinical convergence measures in children enrolled in the Convergence Insufficiency Treatment Trial-Attention and Reading Trial.
Morrison, Ann M; Kulp, Marjean T; Cotter, Susan A; Scheiman, Mitchell M; Jenewein, Erin C; Roberts, Tawna L; Mitchell, G Lynn; Arnold, L Eugene; Retnasothi, Dashaini; Bade, Annette; Hertle, Richard; Borsting, Eric.
Affiliation
  • Morrison AM; The Ohio State University College of Optometry, Columbus, Ohio, USA.
  • Kulp MT; The Ohio State University College of Optometry, Columbus, Ohio, USA.
  • Cotter SA; Southern California College of Optometry at Marshall B. Ketchum University, Fullerton, California, USA.
  • Scheiman MM; Salus University Pennsylvania College of Optometry, Elkins Park, Pennsylvania, USA.
  • Jenewein EC; Salus University Pennsylvania College of Optometry, Elkins Park, Pennsylvania, USA.
  • Roberts TL; Spencer Center for Vision Research, Byers Eye Institute at Stanford University, Palo Alto, California, USA.
  • Mitchell GL; The Ohio State University College of Optometry, Columbus, Ohio, USA.
  • Arnold LE; The Ohio State University College of Medicine, Columbus, Ohio, USA.
  • Retnasothi D; Southern California College of Optometry at Marshall B. Ketchum University, Fullerton, California, USA.
  • Bade A; Nova Southeastern University, Fort Lauderdale, Florida, USA.
  • Hertle R; Akron Children's Hospital, Akron, Ohio, USA.
  • Borsting E; Southern California College of Optometry at Marshall B. Ketchum University, Fullerton, California, USA.
Article in En | MEDLINE | ID: mdl-39141379
ABSTRACT

PURPOSE:

To assess the long-term stability of clinical measures of convergence (near point of convergence [NPC] and positive fusional vergence [PFV]) in participants enrolled in the Convergence Insufficiency Treatment Trial-Attention and Reading Trial (CITT-ART) who received 16 weeks of office-based vergence/accommodative therapy.

METHODS:

A total of 310 children, 9-14 years old, with symptomatic convergence insufficiency were enrolled in CITT-ART. Some 270 completed both their 16-week primary outcome visit followed by a 1-year follow-up visit. Of those 270, 181 (67%) were randomised to the vergence/accommodative therapy. Of the 181 in the vergence/accommodative group, 121 (67%) reported not receiving any additional treatment after the 16-week primary outcome visit. The mean change in NPC, PFV and percentages of children classified by the predetermined success criteria of convergence (normal NPC [<6 cm] and/or improved by ≥4 cm; normal PFV [passing Sheard's criterion and base-out break >15Δ] and/or improved by ≥10Δ) were compared at the 16-week primary outcome visit and 1 year later.

RESULTS:

Of the 121 who returned for their 1-year follow-up visit, there was no significant change in mean adjusted NPC (reduction of -0.2 cm; 95% CI -1.0 to 0.5 cm) at 1 year. There was a statistically significant decrease in mean-adjusted PFV (-4.7∆; 95% CI -6.5 to -2.8Δ) at 1 year. There were similar percentages of participants classified as 'normal' (p = 0.30), 'normal and/or improved' (p > 0.50) and 'normal and improved' (p > 0.14) based on NPC and PFV at the 1-year visit compared with the 16-week primary outcome visit.

CONCLUSION:

The improvements in NPC and PFV following 16 weeks of vergence/accommodative therapy (with no reported additional treatment thereafter) in children with symptomatic convergence insufficiency persisted 1-year post-treatment.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ophthalmic Physiol Opt Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ophthalmic Physiol Opt Year: 2024 Document type: Article Affiliation country: United States