4.6 Article

Visual Consequences of Refractive Errors in the General Population

期刊

OPHTHALMOLOGY
卷 122, 期 1, 页码 101-109

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.ophtha.2014.07.030

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资金

  1. Netherlands Organization of Scientific Research (NWO) [Vidi 91796357]
  2. NWO Investments [175.010.2005.011, 911-03-012]
  3. Netherlands Genomics Initiative (NGI)/ NWO [050-060-810]
  4. Erasmus Medical Center and Erasmus University, Rotterdam, The Netherlands
  5. Netherlands Organization for Health Research and Development (ZonMw)
  6. UitZicht, Stichting Combined Ophthalmic Research Rotterdam (CORR)
  7. Research Institute for Diseases in the Elderly [014-93-015, RIDE2]
  8. Ministry of Education, Culture and Science
  9. Ministry for Health, Welfare and Sports
  10. European Commission (DG XII)
  11. Municipality of Rotterdam
  12. Netherlands Genomics Initiative/ NWO, Rotterdam, The Netherlands
  13. Center for Medical Systems Biology of NGI
  14. Lijf en Leven
  15. M.D. Fonds
  16. Henkes Stichting
  17. Stichting Nederlands Oogheelkundig Onderzoek
  18. Swart van Essen
  19. Bevordering van Volkskracht
  20. Blindenhulp
  21. Landelijke Stichting voor Blinden en Slechtzienden
  22. Rotterdamse Vereniging voor Blindenbelangen
  23. OOG
  24. Algemene Nederlandse Vereniging ter Voorkoming van Blindheid
  25. Rotterdam Eye Hospital Research Foundation
  26. Erasmus Trustfonds
  27. Topcon Europe

向作者/读者索取更多资源

Objective: To study the frequency and causes of visual impairment in relation to refractive error. Design: Population-based cohort study. Participants: A total of 6597 participants from Rotterdam Study I (baseline and 4 follow-up examinations) and 2579 participants from Rotterdam Study II (baseline and 2 follow-up examinations), all 55 years or older, were included. Methods: Participants underwent an extensive ophthalmic examination, including best-corrected visual acuity and objective refraction, fundus photography, visual field perimetry, and optical coherence tomography imaging of macula and optic disc. We calculated cumulative risks and odds ratios of visual impairment for various refractive error categories and determined causes by using all screening information as well as medical records. Main Outcome Measures: Unilateral and bilateral low vision (World Health Organization [WHO] criteria, VA <0.3 and VA >= 0.05; United States (US) criteria, VA <0.5 and VA >= 0.1) and blindness (WHO criteria, VA <0.05; US criteria, VA<0.1). Results: Cumulative risks of visual impairment ranged from virtually 0 in all refractive error categories at 55 years of age to 9.5% (standard error, 0.01) for emmetropia and 15.3% (standard error, 0.06) for high hyperopia to 33.7% (standard error, 0.08) for high myopia at 85 years of age. The major causes of visual impairment in highly hyperopic persons were age-related macular degeneration (AMD), cataract, and combined causes (each 25%); in highly myopic persons, the major cause was myopic macular degeneration (38.9%). The major causes of visual impairment for the other refractive error categories were AMD and cataract. Compared with those with emmetropia, those with high myopia had a significantly increased lifetime risk of visual impairment; those with -6 diopters (D) or less and -10 D or more had an odds ratio (OR) risk of 3.4 (95% confidence interval [CI], 1.4-8.2) of visual impairment; those with less than -10 D had an OR of 22.0 (95% CI, 9.2-52.6). Conclusions: Of all refractive errors, highmyopia has themost severe visual consequences. Irreversiblemacular pathologic features are the most common cause of visual impairment in this group. (C) 2015 by the American Academy of Ophthalmology.

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