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The Test-Retest Variability of the COMPlog System in Participants with Induced Non-Normal Visual Acuity
AIM: The aim of this study was to determine and compare test-retest variability (TRV) of the computerised visual acuity (VA) COMPlog system on participants with normal vision and non-normal vision induced by bangerter foils (BFs). METHODS: Twenty adult volunteers with VA of 0.100 logMAR or better in...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
White Rose University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510395/ https://www.ncbi.nlm.nih.gov/pubmed/32999974 http://dx.doi.org/10.22599/bioj.127 |
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author | Kan, Mun Wei Bjerre, Anne |
author_facet | Kan, Mun Wei Bjerre, Anne |
author_sort | Kan, Mun Wei |
collection | PubMed |
description | AIM: The aim of this study was to determine and compare test-retest variability (TRV) of the computerised visual acuity (VA) COMPlog system on participants with normal vision and non-normal vision induced by bangerter foils (BFs). METHODS: Twenty adult volunteers with VA of 0.100 logMAR or better in each eye and no eye conditions were included. Monocular VA data using the COMPlog system under five conditions—with plain Plano glasses (visually normal condition) and four pairs of Plano glasses with BF strengths of 0.6, 0.3, 0.2 and 0.1 (induced non-normal vision conditions)—were collected on two separate visits. To reduce bias, the eye tested and order of the BFs assessed were randomised. Data comparison was analysed using 2-factor ANOVA and paired t-tests and Bland Altman analysis to assess TRV. RESULTS: Mean VA score from the two visits was –0.072 ± 0.1 logMAR for Plano, 0.106 ± 0.1 logMAR for BF 0.6, 0.428 ± 0.1 logMAR for BF 0.3, 0.662 ± 0.09 logMAR for BF 0.2 and 0.850 ± 0.08 logMAR for BF 0.1. As BF density increased, VA score significantly worsened (p < 0.0001). Overall mean VA score from the first and second visit was 0.410 ± 0.4 logMAR and 0.379 ± 0.4 logMAR, respectively. This improvement was significant (p < 0.009). The 95% limits of agreement of the VA scores between testing conditions had a range of ±0.120 to ±0.220 logMAR. CONCLUSIONS: Increase in BF strength led to a worsened VA score. However, the COMPlog TRV under the visually normal and induced non-normal vision conditions were within a similar range (±0.120 to ±0.220 logMAR). VA significantly improved on the second visit, suggesting a possible learning effect, which could have a clinical impact. |
format | Online Article Text |
id | pubmed-7510395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | White Rose University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-75103952020-09-29 The Test-Retest Variability of the COMPlog System in Participants with Induced Non-Normal Visual Acuity Kan, Mun Wei Bjerre, Anne Br Ir Orthopt J Original Article AIM: The aim of this study was to determine and compare test-retest variability (TRV) of the computerised visual acuity (VA) COMPlog system on participants with normal vision and non-normal vision induced by bangerter foils (BFs). METHODS: Twenty adult volunteers with VA of 0.100 logMAR or better in each eye and no eye conditions were included. Monocular VA data using the COMPlog system under five conditions—with plain Plano glasses (visually normal condition) and four pairs of Plano glasses with BF strengths of 0.6, 0.3, 0.2 and 0.1 (induced non-normal vision conditions)—were collected on two separate visits. To reduce bias, the eye tested and order of the BFs assessed were randomised. Data comparison was analysed using 2-factor ANOVA and paired t-tests and Bland Altman analysis to assess TRV. RESULTS: Mean VA score from the two visits was –0.072 ± 0.1 logMAR for Plano, 0.106 ± 0.1 logMAR for BF 0.6, 0.428 ± 0.1 logMAR for BF 0.3, 0.662 ± 0.09 logMAR for BF 0.2 and 0.850 ± 0.08 logMAR for BF 0.1. As BF density increased, VA score significantly worsened (p < 0.0001). Overall mean VA score from the first and second visit was 0.410 ± 0.4 logMAR and 0.379 ± 0.4 logMAR, respectively. This improvement was significant (p < 0.009). The 95% limits of agreement of the VA scores between testing conditions had a range of ±0.120 to ±0.220 logMAR. CONCLUSIONS: Increase in BF strength led to a worsened VA score. However, the COMPlog TRV under the visually normal and induced non-normal vision conditions were within a similar range (±0.120 to ±0.220 logMAR). VA significantly improved on the second visit, suggesting a possible learning effect, which could have a clinical impact. White Rose University Press 2019-04-11 /pmc/articles/PMC7510395/ /pubmed/32999974 http://dx.doi.org/10.22599/bioj.127 Text en Copyright: © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (CC-BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Article Kan, Mun Wei Bjerre, Anne The Test-Retest Variability of the COMPlog System in Participants with Induced Non-Normal Visual Acuity |
title | The Test-Retest Variability of the COMPlog System in Participants with Induced Non-Normal Visual Acuity |
title_full | The Test-Retest Variability of the COMPlog System in Participants with Induced Non-Normal Visual Acuity |
title_fullStr | The Test-Retest Variability of the COMPlog System in Participants with Induced Non-Normal Visual Acuity |
title_full_unstemmed | The Test-Retest Variability of the COMPlog System in Participants with Induced Non-Normal Visual Acuity |
title_short | The Test-Retest Variability of the COMPlog System in Participants with Induced Non-Normal Visual Acuity |
title_sort | test-retest variability of the complog system in participants with induced non-normal visual acuity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7510395/ https://www.ncbi.nlm.nih.gov/pubmed/32999974 http://dx.doi.org/10.22599/bioj.127 |
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