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Progression of Geographic Atrophy: Retrospective Analysis of Patients from the IRIS® Registry (Intelligent Research in Sight).
Rahimy, Ehsan; Khan, M Ali; Ho, Allen C; Hatfield, Meghan; Nguyen, Thai Hien; Jones, Daniel; McKeown, Alex; Borkar, Durga; Leng, Theodore; Ribeiro, Ramiro; Holekamp, Nancy.
Afiliação
  • Rahimy E; Palo Alto Medical Foundation, Palo Alto, California.
  • Khan MA; Byers Eye Institute at Stanford, Stanford University School of Medicine, Palo Alto, California.
  • Ho AC; Wills Eye Hospital, Philadelphia, Pennsylvania.
  • Hatfield M; Wills Eye Hospital, Philadelphia, Pennsylvania.
  • Nguyen TH; Verana Health, Inc, San Francisco, California.
  • Jones D; Verana Health, Inc, San Francisco, California.
  • McKeown A; Apellis Pharmaceuticals, Inc, Waltham, Massachusetts.
  • Borkar D; Apellis Pharmaceuticals, Inc, Waltham, Massachusetts.
  • Leng T; Duke University School of Medicine, Durham, North Carolina.
  • Ribeiro R; Byers Eye Institute at Stanford, Stanford University School of Medicine, Palo Alto, California.
  • Holekamp N; Apellis Pharmaceuticals, Inc, Waltham, Massachusetts.
Ophthalmol Sci ; 3(4): 100318, 2023 Dec.
Article em En | MEDLINE | ID: mdl-37274013
Purpose: To evaluate disease progression and associated vision changes in patients with geographic atrophy (GA) secondary to age-related macular degeneration (AMD) in 1 eye and GA or neovascular AMD (nAMD) in the fellow eye using a large dataset from routine clinical practice. Design: Retrospective analysis of clinical data over 24 months. Subjects: A total of 256 635 patients with GA from the American Academy of Ophthalmology (Academy) IRIS® Registry (Intelligent Research in Sight) Registry (January 2016 to December 2017). Methods: Patients with ≥ 24 months of follow-up were grouped by fellow-eye status: Cohort 1, GA:GA; Cohort 2, GA:nAMD, each with (subfoveal) and without subfoveal (nonsubfoveal) involvement. Eyes with history of retinal disease other than AMD were excluded. Sensitivity analysis included patients who were managed by retina specialists and had a record of imaging within 30 days of diagnosis. Main Outcome Measures: Change in visual acuity (VA), occurrence of new-onset nAMD, and GA progression from nonsubfoveal to subfoveal. Results: In total, 69 441 patients were included: 44 120 (64%) GA:GA and 25 321 (36%) GA:nAMD. Otherwise eligible patients (57 788) were excluded due to follow-up < 24 months. In both GA:GA and GA:nAMD cohorts, nonsubfoveal study eyes had better mean (standard deviation) VA at index (67 [19.3] and 66 [20.3] letters) than subfoveal eyes (59 [23.9] and 47 [26.9] letters), and 24-month mean VA changes were similar for nonsubfoveal (-7.6 and -6.2) and subfoveal (-7.9 and -6.5) subgroups. Progression to subfoveal GA occurred in 16.7% of nonsubfoveal study eyes in the GA:GA cohort and 12.5% in the GA:nAMD cohort. More new-onset study-eye nAMD was observed in the GA:nAMD (21.6%) versus GA:GA (8.2%) cohorts. Sensitivity analysis supported the robustness of the observations in the study. Conclusions: This retrospective analysis describes the natural progression of GA lesions and the decline in VA associated with the disease. Financial Disclosures: Proprietary or commercial disclosure may be found after the references.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article