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dc.contributor.authorCrewe, Julie
dc.contributor.authorMorgan, W.
dc.contributor.authorMorlet, Nigel
dc.contributor.authorSpilsbury, Katrina
dc.contributor.authorMukhtar, Syed Aqif
dc.contributor.authorClark, Antony
dc.contributor.authorNg, Jonathon
dc.contributor.authorCrowley, Margaret
dc.contributor.authorSemmens, James
dc.date.accessioned2017-01-30T10:49:17Z
dc.date.available2017-01-30T10:49:17Z
dc.date.created2015-03-04T01:07:23Z
dc.date.issued2011
dc.identifier.citationCrewe, J. and Morgan, W. and Morlet, N. and Spilsbury, K. and Mukhtar, S.A. and Clark, A. and Ng, J. et al. 2011. Assessing the diagnostic validity of a blind register. Clinical and Experimental Ophthalmology. 39 (6): pp. 494-500.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/5920
dc.identifier.doi10.1111/j.1442-9071.2011.02509.x
dc.description.abstract

Background:  To validate the accuracy of clinical ophthalmic information held on the West Australian blind register. Design:  Community-based cross-sectional study. Participants:  Legally blind or severely vision-impaired people were selected randomly from the Association for the Blind of Western Australia register. Methods:  Individuals were reviewed by one of two consultant ophthalmologists. Main Outcome Measures:  The positive predictive value (ppv), sensitivity and specificity for legal blindness status and diagnostic causes of vision loss were calculated using data extracted from the Association for the Blind of Western Australia blind register. Results:  273 blind or near blind people were reviewed from the register total of 4271 individuals. There were more women (57%) than men, median age 81 years. For legal blindness status the ppv was 0.88 (95% confidence interval [CI] 0.82–0.92), sensitivity 0.75 (95% CI 0.74–0.84) and specificity 0.6 (95% CI 0.46–0.73). The ppv for the diagnostic causes of blindness were: age-related macular degeneration = 0.95 (95% CI 0.91–0.97), retinitis pigmentosa ppv = 1 (95% CI 0.81–1.0), diabetic retinopathy ppv = 0.9 (95% CI 0.57–0.99), optic neuropathies ppv = 0.77 (95% CI 0.51–0.92) and glaucoma ppv = 0.87 (95% CI 0.7–0.96). Forty individuals (15%) had treatable conditions contributing to their vision loss. Conclusions:  The blind register diagnoses and legal blindness status are of high accuracy. This information allows useful linkages to other databases for studies of blindness interactions. A regular updating mechanism would improve the future accuracy of this valuable regional asset. The presence of untreated cataract suggests that regular follow up and appropriate treatment may help optimize vision in blind patients.

dc.publisherWiley-Blackwell Publishing Asia
dc.titleAssessing the diagnostic validity of a blind register
dc.typeJournal Article
dcterms.source.volume39
dcterms.source.number6
dcterms.source.startPage494
dcterms.source.endPage500
dcterms.source.issn14426404
dcterms.source.titleClinical and Experimental Ophthalmology
curtin.departmentCentre for Population Health Research
curtin.accessStatusFulltext not available


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