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Volume 108, Issue 11, Pages 1966-1972 (November 2001)


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Prevalence and predictors of open-angle glaucoma: Results from the visual impairment project

LeAnn M Weih, PhD, MScCorresponding Author Informationaemail address, Mukesh Nanjan, PhD (MPhil)a, Catherine A McCarty, PhD, MPHa, Hugh R Taylor, MD (FRACO)a

Received 7 April 2000; accepted 13 June 2001.

Abstract 

Purpose

To determine the prevalence and investigate predictors of open-angle glaucoma in Victoria, Australia.

Design

Two-site, population-based cross-sectional study.

Participants

Permanent residents aged 40 years and older at recruitment from 1992 through 1996.

Methods

A cluster-stratified random sample of 4744 participants from two cohorts, urban and rural, participated. Participants completed a standardized interview regarding demographic, lifestyle, and medical characteristics and a dilated eye examination including measurement of intraocular pressure, visual fields, cup-to-disc ratios, and paired stereo photography of the optic discs. A consensus panel of six ophthalmologists determined glaucoma diagnosis.

Main outcome measure

Diagnosis of glaucoma (possible, probable, definite).

Results

The prevalence of possible glaucoma cases was 1.2% (95% confidence interval [CI], 0.60, 1.7), of probable cases was 0.70% (95% CI, 0.39, 1.0), and of definite cases was 1.8% (95% CI, 1.4, 2.2). There was a significant increase in glaucoma prevalence with age across all definitions, but there was no difference in age-standardized rates between genders. A total of 60% of probable and definite glaucoma cases were undiagnosed before this study. Adjusted for age, the strongest risk factor for glaucoma was a positive family history of glaucoma (odds ratio, 3.1; 95% CI, 1.6, 5.3). Glaucoma patients who had not attended an eye care provider in the last 2 years were eight times (95% CI, 3.2, 20.4) more likely to have undiagnosed disease.

Conclusions

These results support the importance of the genetic or familial basis of many glaucoma cases and highlight the need to develop appropriate techniques to screen for undiagnosed disease.

Manuscript no. 200228.

a Centre for Eye Research Australia, University of Melbourne, Melbourne, Victoria, Australia

Corresponding Author InformationCorrespondence to LeAnn M. Weih, PhD, MSc, Centre for Eye Research Australia, Department of Ophthalmology, The University of Melbourne, Royal Victorian Eye and Ear Hospital, 32 Gisborne Street, East Melbourne, Victoria 3002, Australia

 The authors have no commercial interests in the products or devices mentioned herein.

PII: S0161-6420(01)00799-0


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