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Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry

INTRODUCTION: Understanding the progression to geographic atrophy (GA) in late dry age-related macular degeneration (dAMD) can support development opportunities for dAMD treatments. We characterized dAMD by distribution of visual acuity (VA) categories and evaluated VA progression risk by disease st...

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Autores principales: Leng, Theodore, Schwartz, Jason, Nimke, David, Gallivan, Mark, Fevrier, Helene, Rozario, Nigel, Schultz, Neil M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834463/
https://www.ncbi.nlm.nih.gov/pubmed/36369619
http://dx.doi.org/10.1007/s40123-022-00583-y
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author Leng, Theodore
Schwartz, Jason
Nimke, David
Gallivan, Mark
Fevrier, Helene
Rozario, Nigel
Schultz, Neil M.
author_facet Leng, Theodore
Schwartz, Jason
Nimke, David
Gallivan, Mark
Fevrier, Helene
Rozario, Nigel
Schultz, Neil M.
author_sort Leng, Theodore
collection PubMed
description INTRODUCTION: Understanding the progression to geographic atrophy (GA) in late dry age-related macular degeneration (dAMD) can support development opportunities for dAMD treatments. We characterized dAMD by distribution of visual acuity (VA) categories and evaluated VA progression risk by disease stage. METHODS: This retrospective observational study used data from the American Academy of Ophthalmology IRIS(®) Registry (Intelligent Research in Sight) to identify patients diagnosed with dAMD in ≥ 1 eye from January 2016 through December 2019 (index date) with ≥ 1 visit and ≥ 1 VA measurement recorded post-index date. Patients were followed until the date of last visit, last contribution for diagnosing provider, or diagnosis of neovascular AMD post-index. Models were utilized to describe the distribution of VA categories and progression to worsening VA. RESULTS: Data from 593,277 patients were analyzed. At baseline, 64.4% had mild disease, 29.4% intermediate, and 2.9%/3.3% had GA with/without subfoveal involvement. Most patients with mild (88.4%) and intermediate (79.7%) disease and GA without subfoveal involvement (57.1%) had baseline VA ≥ 20/63 in the study eye; 72.0% of patients with GA with subfoveal involvement had VA < 20/63. Modeled results showed lower VA with more progressive stage at baseline. Annual probability of stable dAMD based on baseline stage ranged from 82.1% (GA without) to 92.3% (GA with subfoveal involvement). Annual progression probability to GA without/with subfoveal involvement was 0.4% for mild and 5.5% for intermediate disease and from dry to neovascular AMD, 0.5% for mild and 8.0% for intermediate disease. CONCLUSIONS: Results from this analysis of a large database of electronic health records complement those from randomized trials and show that patients with more advanced dAMD have lower VA at baseline and that VA progression is generally faster with each progressive stage. Together these findings highlight the disease burden and trajectory of dAMD as well as opportunities for addressing unmet needs. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-98344632023-01-13 Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry Leng, Theodore Schwartz, Jason Nimke, David Gallivan, Mark Fevrier, Helene Rozario, Nigel Schultz, Neil M. Ophthalmol Ther Original Research INTRODUCTION: Understanding the progression to geographic atrophy (GA) in late dry age-related macular degeneration (dAMD) can support development opportunities for dAMD treatments. We characterized dAMD by distribution of visual acuity (VA) categories and evaluated VA progression risk by disease stage. METHODS: This retrospective observational study used data from the American Academy of Ophthalmology IRIS(®) Registry (Intelligent Research in Sight) to identify patients diagnosed with dAMD in ≥ 1 eye from January 2016 through December 2019 (index date) with ≥ 1 visit and ≥ 1 VA measurement recorded post-index date. Patients were followed until the date of last visit, last contribution for diagnosing provider, or diagnosis of neovascular AMD post-index. Models were utilized to describe the distribution of VA categories and progression to worsening VA. RESULTS: Data from 593,277 patients were analyzed. At baseline, 64.4% had mild disease, 29.4% intermediate, and 2.9%/3.3% had GA with/without subfoveal involvement. Most patients with mild (88.4%) and intermediate (79.7%) disease and GA without subfoveal involvement (57.1%) had baseline VA ≥ 20/63 in the study eye; 72.0% of patients with GA with subfoveal involvement had VA < 20/63. Modeled results showed lower VA with more progressive stage at baseline. Annual probability of stable dAMD based on baseline stage ranged from 82.1% (GA without) to 92.3% (GA with subfoveal involvement). Annual progression probability to GA without/with subfoveal involvement was 0.4% for mild and 5.5% for intermediate disease and from dry to neovascular AMD, 0.5% for mild and 8.0% for intermediate disease. CONCLUSIONS: Results from this analysis of a large database of electronic health records complement those from randomized trials and show that patients with more advanced dAMD have lower VA at baseline and that VA progression is generally faster with each progressive stage. Together these findings highlight the disease burden and trajectory of dAMD as well as opportunities for addressing unmet needs. GRAPHICAL ABSTRACT: [Image: see text] Springer Healthcare 2022-11-11 2023-02 /pmc/articles/PMC9834463/ /pubmed/36369619 http://dx.doi.org/10.1007/s40123-022-00583-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Leng, Theodore
Schwartz, Jason
Nimke, David
Gallivan, Mark
Fevrier, Helene
Rozario, Nigel
Schultz, Neil M.
Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry
title Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry
title_full Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry
title_fullStr Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry
title_full_unstemmed Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry
title_short Dry Age-Related Macular Degeneration: Distribution of Visual Acuity and Progression Risk in a Large Registry
title_sort dry age-related macular degeneration: distribution of visual acuity and progression risk in a large registry
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834463/
https://www.ncbi.nlm.nih.gov/pubmed/36369619
http://dx.doi.org/10.1007/s40123-022-00583-y
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