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Intersession test–retest variability of 10-2 MAIA microperimetry in fixation-threatening glaucoma

PURPOSE: To determine the intersession test–retest variability (TRV) of CenterVue Macular Integrity Assessment (MAIA) microperimeter in glaucoma patients with fixation-threatening field defects. METHODS: This is a prospective case–control study of 27 participants consisting of 13 patients with stabl...

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Autores principales: Wong, Evan N, Morgan, William H, Chen, Fred K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404802/
https://www.ncbi.nlm.nih.gov/pubmed/28461736
http://dx.doi.org/10.2147/OPTH.S131371
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author Wong, Evan N
Morgan, William H
Chen, Fred K
author_facet Wong, Evan N
Morgan, William H
Chen, Fred K
author_sort Wong, Evan N
collection PubMed
description PURPOSE: To determine the intersession test–retest variability (TRV) of CenterVue Macular Integrity Assessment (MAIA) microperimeter in glaucoma patients with fixation-threatening field defects. METHODS: This is a prospective case–control study of 27 participants consisting of 13 patients with stable primary open-angle glaucoma and 14 control subjects including 5 healthy individuals and 9 retinal patients (5 with non-neovascular age-related macular degeneration and 4 with inherited retinal disease). Each participant underwent three microperimetry tests in one eye at 1-month intervals. Each test used an identical test strategy of 10-2 Cartesian grid and 4-2 staircase algorithm. We investigated TRV by calculating the coefficient of repeatability (CR) for mean sensitivity (MS) and point-wise sensitivity (PWS) for glaucomatous subjects and retinal and normal subjects. 95% confidence intervals (CIs) for CRs were calculated. RESULTS: There was no significant change in MS, and the median durations of microperimetry sessions were 9′26″, 8′52″, and 8′46″ across the three study visits. The intersession CRs for MS were 1.1, 2.5, and 1.8 dB, and the average CRs for PWS were 3.5, 7.4, and 8.6 dB for healthy controls and retinal and glaucoma patients, respectively. For test loci with 25–34 dB at baseline, CRs for PWS were 8.2 (95% CI: 7.5–8.9) and 4.3 (95% CI: 4.0–4.6) dB for glaucoma and control subjects, respectively. CONCLUSION: We found differences in TRV of test loci depending on the baseline sensitivity value. Glaucoma patients had significantly worse TRV for loci that had sensitivity values within the normal range at baseline. The estimated CR has implications for sample size calculation in future glaucoma treatment trials using microperimetry as a clinical endpoint.
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spelling pubmed-54048022017-05-01 Intersession test–retest variability of 10-2 MAIA microperimetry in fixation-threatening glaucoma Wong, Evan N Morgan, William H Chen, Fred K Clin Ophthalmol Original Research PURPOSE: To determine the intersession test–retest variability (TRV) of CenterVue Macular Integrity Assessment (MAIA) microperimeter in glaucoma patients with fixation-threatening field defects. METHODS: This is a prospective case–control study of 27 participants consisting of 13 patients with stable primary open-angle glaucoma and 14 control subjects including 5 healthy individuals and 9 retinal patients (5 with non-neovascular age-related macular degeneration and 4 with inherited retinal disease). Each participant underwent three microperimetry tests in one eye at 1-month intervals. Each test used an identical test strategy of 10-2 Cartesian grid and 4-2 staircase algorithm. We investigated TRV by calculating the coefficient of repeatability (CR) for mean sensitivity (MS) and point-wise sensitivity (PWS) for glaucomatous subjects and retinal and normal subjects. 95% confidence intervals (CIs) for CRs were calculated. RESULTS: There was no significant change in MS, and the median durations of microperimetry sessions were 9′26″, 8′52″, and 8′46″ across the three study visits. The intersession CRs for MS were 1.1, 2.5, and 1.8 dB, and the average CRs for PWS were 3.5, 7.4, and 8.6 dB for healthy controls and retinal and glaucoma patients, respectively. For test loci with 25–34 dB at baseline, CRs for PWS were 8.2 (95% CI: 7.5–8.9) and 4.3 (95% CI: 4.0–4.6) dB for glaucoma and control subjects, respectively. CONCLUSION: We found differences in TRV of test loci depending on the baseline sensitivity value. Glaucoma patients had significantly worse TRV for loci that had sensitivity values within the normal range at baseline. The estimated CR has implications for sample size calculation in future glaucoma treatment trials using microperimetry as a clinical endpoint. Dove Medical Press 2017-04-20 /pmc/articles/PMC5404802/ /pubmed/28461736 http://dx.doi.org/10.2147/OPTH.S131371 Text en © 2017 Wong et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wong, Evan N
Morgan, William H
Chen, Fred K
Intersession test–retest variability of 10-2 MAIA microperimetry in fixation-threatening glaucoma
title Intersession test–retest variability of 10-2 MAIA microperimetry in fixation-threatening glaucoma
title_full Intersession test–retest variability of 10-2 MAIA microperimetry in fixation-threatening glaucoma
title_fullStr Intersession test–retest variability of 10-2 MAIA microperimetry in fixation-threatening glaucoma
title_full_unstemmed Intersession test–retest variability of 10-2 MAIA microperimetry in fixation-threatening glaucoma
title_short Intersession test–retest variability of 10-2 MAIA microperimetry in fixation-threatening glaucoma
title_sort intersession test–retest variability of 10-2 maia microperimetry in fixation-threatening glaucoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5404802/
https://www.ncbi.nlm.nih.gov/pubmed/28461736
http://dx.doi.org/10.2147/OPTH.S131371
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