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Validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model
Current tests for assessing metamorphopsia do not account for confounders such as perceptual filling-in and spatial redundancy, which affect its sensitivity and repeatability. This proof-of-concept study aimed to assess the performance of a novel laboratory-based psychophysical test (Line Sag Test,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484749/ https://www.ncbi.nlm.nih.gov/pubmed/32913214 http://dx.doi.org/10.1038/s41598-020-71627-1 |
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author | Wang, Henrietta Khuu, Sieu K. Lam, Sheila Lin, Clarissa Kalloniatis, Michael Phu, Jack |
author_facet | Wang, Henrietta Khuu, Sieu K. Lam, Sheila Lin, Clarissa Kalloniatis, Michael Phu, Jack |
author_sort | Wang, Henrietta |
collection | PubMed |
description | Current tests for assessing metamorphopsia do not account for confounders such as perceptual filling-in and spatial redundancy, which affect its sensitivity and repeatability. This proof-of-concept study aimed to assess the performance of a novel laboratory-based psychophysical test (Line Sag Test, LST) which addresses these issues for quantification of metamorphopsia in idiopathic epiretinal membranes. The LST quantifies perpendicular metamorphopsia at three eccentricities (3°, 6°, and 9°) along eight meridians (45° steps). Metamorphopsia was assessed using the LST and Amsler grid and the hit rates of both tests for detecting metamorphopsia were compared. Normal metamorphopsia scores using the LST did not differ significantly from 0 and fell within one step-size (p = 0.500). The LST detected significantly more cases of metamorphopsia than the Amsler grid (14/21 versus 3/21) (p = 0.003). Similarly, significantly more cases of visual distortions in asymptomatic iERMs were detected using the LST than the Amsler grid (11/18 versus 0/18) (p = 0.008). The LST has a higher hit rate compared to the Amsler grid (67% versus 14%). This work demonstrates a psychophysically-robust functional test addressing perceptual confounders is more sensitive for quantifying and localising metamorphopsia in macular disease, particularly in asymptomatic disease. |
format | Online Article Text |
id | pubmed-7484749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74847492020-09-15 Validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model Wang, Henrietta Khuu, Sieu K. Lam, Sheila Lin, Clarissa Kalloniatis, Michael Phu, Jack Sci Rep Article Current tests for assessing metamorphopsia do not account for confounders such as perceptual filling-in and spatial redundancy, which affect its sensitivity and repeatability. This proof-of-concept study aimed to assess the performance of a novel laboratory-based psychophysical test (Line Sag Test, LST) which addresses these issues for quantification of metamorphopsia in idiopathic epiretinal membranes. The LST quantifies perpendicular metamorphopsia at three eccentricities (3°, 6°, and 9°) along eight meridians (45° steps). Metamorphopsia was assessed using the LST and Amsler grid and the hit rates of both tests for detecting metamorphopsia were compared. Normal metamorphopsia scores using the LST did not differ significantly from 0 and fell within one step-size (p = 0.500). The LST detected significantly more cases of metamorphopsia than the Amsler grid (14/21 versus 3/21) (p = 0.003). Similarly, significantly more cases of visual distortions in asymptomatic iERMs were detected using the LST than the Amsler grid (11/18 versus 0/18) (p = 0.008). The LST has a higher hit rate compared to the Amsler grid (67% versus 14%). This work demonstrates a psychophysically-robust functional test addressing perceptual confounders is more sensitive for quantifying and localising metamorphopsia in macular disease, particularly in asymptomatic disease. Nature Publishing Group UK 2020-09-10 /pmc/articles/PMC7484749/ /pubmed/32913214 http://dx.doi.org/10.1038/s41598-020-71627-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wang, Henrietta Khuu, Sieu K. Lam, Sheila Lin, Clarissa Kalloniatis, Michael Phu, Jack Validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model |
title | Validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model |
title_full | Validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model |
title_fullStr | Validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model |
title_full_unstemmed | Validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model |
title_short | Validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model |
title_sort | validation of a novel functional test for assessing metamorphopsia using epiretinal membranes as a model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7484749/ https://www.ncbi.nlm.nih.gov/pubmed/32913214 http://dx.doi.org/10.1038/s41598-020-71627-1 |
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