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Visual impairment and vision‐related quality of life in the Early Manifest Glaucoma Trial after 20 years of follow‐up
PURPOSE: To determine the association between vision‐related quality of life (VRQOL) and levels of visual function loss in the Early Manifest Glaucoma Trial (EMGT). METHODS: Two hundred and fifty‐five patients were included in the EMGT between 1993 and 1997 and followed regularly by ophthalmic exami...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014208/ https://www.ncbi.nlm.nih.gov/pubmed/26382936 http://dx.doi.org/10.1111/aos.12839 |
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author | Peters, Dorothea Heijl, Anders Brenner, Lena Bengtsson, Boel |
author_facet | Peters, Dorothea Heijl, Anders Brenner, Lena Bengtsson, Boel |
author_sort | Peters, Dorothea |
collection | PubMed |
description | PURPOSE: To determine the association between vision‐related quality of life (VRQOL) and levels of visual function loss in the Early Manifest Glaucoma Trial (EMGT). METHODS: Two hundred and fifty‐five patients were included in the EMGT between 1993 and 1997 and followed regularly by ophthalmic examinations. A Swedish translation of the National Eye Institute Visual Function Questionnaire 25 (NEI VFQ‐25) was self‐administered at several follow‐up visits until 2014. We analysed the association between Rasch‐calibrated NEI VFQ‐25 scores and visual function in the best eye at the final follow‐up visit. RESULTS: Ninety‐one per cent (233/255) of all participants completed the NEI VFQ‐25 at least once. In univariate logistic regression analysis, NEI VFQ‐25 scores were modestly associated with visual acuity (VA) (r (2) = 0.330, p < 0.001), visual field index (VFI) (r (2) = 0.200, p < 0.001) and perimetric mean deviation (MD) (r (2) = 0.193, p < 0.001). In multivariate analysis, VA and VFI together accounted for approximately 40% (r (2) = 0.380) of the NEI VFQ‐25 scores. NEI VFQ‐25 scores were significantly higher for patients with no visual impairment (mean 73 ± 22) than for visually impaired patients (mean 31 ± 15, p < 0.001). VFI worse than 50% or MD worse than −18 dB was significantly associated with low VRQOL scores (p < 0.001). CONCLUSIONS: Our results support the widespread, albeit arbitrary, use of a better‐eye visual field of <50% as an important threshold for a significant reduction in VRQOL. |
format | Online Article Text |
id | pubmed-5014208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50142082016-09-23 Visual impairment and vision‐related quality of life in the Early Manifest Glaucoma Trial after 20 years of follow‐up Peters, Dorothea Heijl, Anders Brenner, Lena Bengtsson, Boel Acta Ophthalmol Original Articles PURPOSE: To determine the association between vision‐related quality of life (VRQOL) and levels of visual function loss in the Early Manifest Glaucoma Trial (EMGT). METHODS: Two hundred and fifty‐five patients were included in the EMGT between 1993 and 1997 and followed regularly by ophthalmic examinations. A Swedish translation of the National Eye Institute Visual Function Questionnaire 25 (NEI VFQ‐25) was self‐administered at several follow‐up visits until 2014. We analysed the association between Rasch‐calibrated NEI VFQ‐25 scores and visual function in the best eye at the final follow‐up visit. RESULTS: Ninety‐one per cent (233/255) of all participants completed the NEI VFQ‐25 at least once. In univariate logistic regression analysis, NEI VFQ‐25 scores were modestly associated with visual acuity (VA) (r (2) = 0.330, p < 0.001), visual field index (VFI) (r (2) = 0.200, p < 0.001) and perimetric mean deviation (MD) (r (2) = 0.193, p < 0.001). In multivariate analysis, VA and VFI together accounted for approximately 40% (r (2) = 0.380) of the NEI VFQ‐25 scores. NEI VFQ‐25 scores were significantly higher for patients with no visual impairment (mean 73 ± 22) than for visually impaired patients (mean 31 ± 15, p < 0.001). VFI worse than 50% or MD worse than −18 dB was significantly associated with low VRQOL scores (p < 0.001). CONCLUSIONS: Our results support the widespread, albeit arbitrary, use of a better‐eye visual field of <50% as an important threshold for a significant reduction in VRQOL. John Wiley and Sons Inc. 2015-09-18 2015-12 /pmc/articles/PMC5014208/ /pubmed/26382936 http://dx.doi.org/10.1111/aos.12839 Text en © 2015 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Peters, Dorothea Heijl, Anders Brenner, Lena Bengtsson, Boel Visual impairment and vision‐related quality of life in the Early Manifest Glaucoma Trial after 20 years of follow‐up |
title | Visual impairment and vision‐related quality of life in the Early Manifest Glaucoma Trial after 20 years of follow‐up |
title_full | Visual impairment and vision‐related quality of life in the Early Manifest Glaucoma Trial after 20 years of follow‐up |
title_fullStr | Visual impairment and vision‐related quality of life in the Early Manifest Glaucoma Trial after 20 years of follow‐up |
title_full_unstemmed | Visual impairment and vision‐related quality of life in the Early Manifest Glaucoma Trial after 20 years of follow‐up |
title_short | Visual impairment and vision‐related quality of life in the Early Manifest Glaucoma Trial after 20 years of follow‐up |
title_sort | visual impairment and vision‐related quality of life in the early manifest glaucoma trial after 20 years of follow‐up |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014208/ https://www.ncbi.nlm.nih.gov/pubmed/26382936 http://dx.doi.org/10.1111/aos.12839 |
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