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Visual acuity impairment in patients with retinitis pigmentosa at age 45 years or older
Abstract
Objective To determine the severity of visual acuity impairment in patients, age 45 years or older, with either isolated or identifiable genetic subtypes of retinitis pigmentosa (RP) and Usher syndrome.Design Multicenter, retrospective, cross-sectional analysis.Participants Visual acuity data were obtained on 999 patients with different genetic subtypes of RP and Usher syndrome, age 45 years or older, from 4 major eye care centers in the United States.Intervention The best-corrected visual acuity obtained on these patients from the eye with better vision on their most recent visit was used for the analysis.Main outcome measure Best-corrected visual acuity was the main parameter analyzed for the study, and it was obtained with Snellen or Feinbloom low vision charts or with a B-VAT II monitor (Mentor).Results The final analyses were done on 982 patients (17 patients with a sector form of RP were analyzed separately). Of the 982 patients, 506 (52%) had a visual acuity of 20/40 or better, and 678 (69%) had a visual acuity of 20/70 or better in at least one eye. There were 243 (25%) patients who had a visual acuity of 20/200 or worse in both eyes. Five (0.5%) patients had no light perception in both eyes. The odds ratio for any patient having a visual acuity of 20/200 or worse in this population was 1.4 for each difference of 10 years of age. Similarly, the odds ratio of a patient having a visual acuity of 20/40 or better in at least one eye was 0.95 for a 10-year age difference.Conclusions In this large population of patients with RP and Usher syndrome from four centers, it was rare for such patients to lose all vision in both eyes. One fourth of the patients had a visual acuity of 20/200 or worse in both eyes, and more than half of the population had a visual acuity of 20/40 or better in at least one eye. These data can be used to counsel such patients on the extent of potential visual acuity impairment from their disease.
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“The number of people affected by RP is estimated to be about 1.5-2 million [226], but only 12% of these have a visual acuity worse than counting fingers and 0.5% have no perception of light [227].”
From Advances in visual prostheses: engineering and biological challenges (2022) · cites this paper as [227]
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Metadata
- Authors
- Grover, S., Fishman, G. A., Anderson, R. J., Tozatti, M. S. V., Heckenlively, J. R., Weleber, R. G., Edwards, A. O., & Brown, J.
- Affiliations
- University of Illinois Chicago (US)
- Universidade de São Paulo (BR)
- University of California, Los Angeles (US)
- Oregon Health & Science University (US)
- The University of Texas Southwestern Medical Center (US)
- University of Iowa (US)
- Corresponding author
- Fishman, Gerald A
- Venue
- Ophthalmology
- Publisher
- Elsevier BV
- Published
- 1999-09
- Volume
- 106
- Issue
- 9
- Pages
- 1780-1785
- ISSN
- 0161-6420 (ISSN-L)
- OpenAlex
- W2131014421
- Cited by
- 235
- References
- 21
- Citations by year
- 2026: 11 · 2025: 17 · 2024: 12 · 2023: 15 · 2022: 17 · 2021: 19 · 2020: 21 · 2019: 14 · 2018: 19 · 2017: 13 · 2016: 10 · 2015: 6 · 2014: 7 · 2013: 8 · 2012: 4
- FWCI
- 0.69
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Ophthalmology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
- Health Sciences › Medicine › Ophthalmology › Glaucoma and retinal disorders
- Keywords
- retinitis pigmentosa, Usher syndrome, visual acuity loss, best-corrected visual acuity, visual prognosis, low vision
- MeSH terms
- Aged, Aged, 80 and over, Cross-Sectional Studies, Female, Hearing Loss, Sensorineural, Humans, Male, Middle Aged, Retinitis Pigmentosa, Retrospective Studies, Severity of Illness Index, Syndrome, Vision Disorders, Visual Acuity, Cohort Studies
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