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Systematic Underestimation of Visual Sensitivity Loss on Microperimetry: Implications for Testing Protocols in Clinical Trials

PURPOSE: To examine whether systematic changes in visual sensitivity measurements on microperimetry occur over tests within the same session and whether these changes vary according to the level of visual sensitivity loss. METHODS: Eighty individuals with glaucoma or atrophic age-related macular deg...

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Autores principales: Wu, Zhichao, Hadoux, Xavier, Jannaud, Maxime, Martin, Keith R., van Wijngaarden, Peter, Guymer, Robyn H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341291/
https://www.ncbi.nlm.nih.gov/pubmed/37428130
http://dx.doi.org/10.1167/tvst.12.7.11
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author Wu, Zhichao
Hadoux, Xavier
Jannaud, Maxime
Martin, Keith R.
van Wijngaarden, Peter
Guymer, Robyn H.
author_facet Wu, Zhichao
Hadoux, Xavier
Jannaud, Maxime
Martin, Keith R.
van Wijngaarden, Peter
Guymer, Robyn H.
author_sort Wu, Zhichao
collection PubMed
description PURPOSE: To examine whether systematic changes in visual sensitivity measurements on microperimetry occur over tests within the same session and whether these changes vary according to the level of visual sensitivity loss. METHODS: Eighty individuals with glaucoma or atrophic age-related macular degeneration underwent three microperimetry tests in one eye during one session using the 4-2 staircase strategy. Changes in mean sensitivity (MS) and pointwise sensitivity (PWS) between the first and second test pairs were examined, with PWS was examined separately based on its average value across the three tests in 6-dB bins. The coefficient of repeatability (CoR) for MS between each sequential test pair was also calculated. RESULTS: There was a significant decline in MS from the first to second test (P = 0.001), but no significant difference in MS was seen between the second and third tests (P = 0.562). This significant decline in the first test pair was observed in locations with an average PWS of <6 dB or between 6 to 12 dB and between 12 to 18 dB (P < 0.001), but not for all other average PWS bins (P ≥ 0.337). The CoR of MS was significantly lower in the second compared to the first test pair (1.4 dB and 2.5 dB, respectively; P < 0.001). CONCLUSIONS: The 4-2 staircase strategy conventionally used on microperimetry testing systematically underestimates visual sensitivity loss on the first test. TRANSLATIONAL RELEVANCE: The consistency and accuracy of visual sensitivity measurements on microperimetry in clinical trials could be markedly improved by using estimates from an initial test to seed subsequent tests and excluding this first test from analyses.
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spelling pubmed-103412912023-07-14 Systematic Underestimation of Visual Sensitivity Loss on Microperimetry: Implications for Testing Protocols in Clinical Trials Wu, Zhichao Hadoux, Xavier Jannaud, Maxime Martin, Keith R. van Wijngaarden, Peter Guymer, Robyn H. Transl Vis Sci Technol Retina PURPOSE: To examine whether systematic changes in visual sensitivity measurements on microperimetry occur over tests within the same session and whether these changes vary according to the level of visual sensitivity loss. METHODS: Eighty individuals with glaucoma or atrophic age-related macular degeneration underwent three microperimetry tests in one eye during one session using the 4-2 staircase strategy. Changes in mean sensitivity (MS) and pointwise sensitivity (PWS) between the first and second test pairs were examined, with PWS was examined separately based on its average value across the three tests in 6-dB bins. The coefficient of repeatability (CoR) for MS between each sequential test pair was also calculated. RESULTS: There was a significant decline in MS from the first to second test (P = 0.001), but no significant difference in MS was seen between the second and third tests (P = 0.562). This significant decline in the first test pair was observed in locations with an average PWS of <6 dB or between 6 to 12 dB and between 12 to 18 dB (P < 0.001), but not for all other average PWS bins (P ≥ 0.337). The CoR of MS was significantly lower in the second compared to the first test pair (1.4 dB and 2.5 dB, respectively; P < 0.001). CONCLUSIONS: The 4-2 staircase strategy conventionally used on microperimetry testing systematically underestimates visual sensitivity loss on the first test. TRANSLATIONAL RELEVANCE: The consistency and accuracy of visual sensitivity measurements on microperimetry in clinical trials could be markedly improved by using estimates from an initial test to seed subsequent tests and excluding this first test from analyses. The Association for Research in Vision and Ophthalmology 2023-07-10 /pmc/articles/PMC10341291/ /pubmed/37428130 http://dx.doi.org/10.1167/tvst.12.7.11 Text en Copyright 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Retina
Wu, Zhichao
Hadoux, Xavier
Jannaud, Maxime
Martin, Keith R.
van Wijngaarden, Peter
Guymer, Robyn H.
Systematic Underestimation of Visual Sensitivity Loss on Microperimetry: Implications for Testing Protocols in Clinical Trials
title Systematic Underestimation of Visual Sensitivity Loss on Microperimetry: Implications for Testing Protocols in Clinical Trials
title_full Systematic Underestimation of Visual Sensitivity Loss on Microperimetry: Implications for Testing Protocols in Clinical Trials
title_fullStr Systematic Underestimation of Visual Sensitivity Loss on Microperimetry: Implications for Testing Protocols in Clinical Trials
title_full_unstemmed Systematic Underestimation of Visual Sensitivity Loss on Microperimetry: Implications for Testing Protocols in Clinical Trials
title_short Systematic Underestimation of Visual Sensitivity Loss on Microperimetry: Implications for Testing Protocols in Clinical Trials
title_sort systematic underestimation of visual sensitivity loss on microperimetry: implications for testing protocols in clinical trials
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341291/
https://www.ncbi.nlm.nih.gov/pubmed/37428130
http://dx.doi.org/10.1167/tvst.12.7.11
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