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Effects of Criterion Bias on Perimetric Sensitivity and Response Variability in Glaucoma

PURPOSE: The purpose of this study was to isolate and quantify the effects of observer response criterion on perimetric sensitivity, response variability, and maximum response probability. METHODS: Twelve people with glaucoma were tested at three locations in the visual field (age = 47–77 years, mea...

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Autores principales: Rubinstein, Nikki J., Turpin, Andrew, Denniss, Jonathan, McKendrick, Allison M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804569/
https://www.ncbi.nlm.nih.gov/pubmed/33510957
http://dx.doi.org/10.1167/tvst.10.1.18
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author Rubinstein, Nikki J.
Turpin, Andrew
Denniss, Jonathan
McKendrick, Allison M.
author_facet Rubinstein, Nikki J.
Turpin, Andrew
Denniss, Jonathan
McKendrick, Allison M.
author_sort Rubinstein, Nikki J.
collection PubMed
description PURPOSE: The purpose of this study was to isolate and quantify the effects of observer response criterion on perimetric sensitivity, response variability, and maximum response probability. METHODS: Twelve people with glaucoma were tested at three locations in the visual field (age = 47–77 years, mean deviation = −0.61 to −14.54 dB, test location Humphrey field analyzer [HFA] sensitivities = 1 to 30 dB). Frequency of seeing (FoS) curves were measured using a method of constant stimuli with two response paradigms: a “yes-no” paradigm similar to static automated perimetry and a criterion-free two interval forced choice (2IFC) paradigm. Comparison measures of sensitivity, maximum response probability, and response variability were derived from the fitted FoS curves. RESULTS: Sensitivity differences between the tasks varied widely (range = −11.3 dB to 21.6 dB) and did not correlate with visual field sensitivity nor whether the visual field location was in an area of steep sensitivity gradient within the visual field. Due to the wide variation in differences between the methods, there was no significant difference in mean sensitivity between the 2IFC task relative to the yes-no task, but a trend for higher sensitivity (mean = 1.9 dB, SD = 6.0 dB, P = 0.11). Response variability and maximum response probability did not differ between the tasks (P > 0.99 and 0.95, respectively). CONCLUSIONS: Perimetric sensitivity estimates are demonstrably altered by observer response criterion but the effect varies widely and unpredictably, even within a single test. Response bias should be considered a factor in perimetric test variability and when comparing sensitivities to nonperimetric data. TRANSLATIONAL RELEVANCE: The effect of response criterion on perimetric response variability varies widely and unpredictably, even within a single test.
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spelling pubmed-78045692021-01-27 Effects of Criterion Bias on Perimetric Sensitivity and Response Variability in Glaucoma Rubinstein, Nikki J. Turpin, Andrew Denniss, Jonathan McKendrick, Allison M. Transl Vis Sci Technol Article PURPOSE: The purpose of this study was to isolate and quantify the effects of observer response criterion on perimetric sensitivity, response variability, and maximum response probability. METHODS: Twelve people with glaucoma were tested at three locations in the visual field (age = 47–77 years, mean deviation = −0.61 to −14.54 dB, test location Humphrey field analyzer [HFA] sensitivities = 1 to 30 dB). Frequency of seeing (FoS) curves were measured using a method of constant stimuli with two response paradigms: a “yes-no” paradigm similar to static automated perimetry and a criterion-free two interval forced choice (2IFC) paradigm. Comparison measures of sensitivity, maximum response probability, and response variability were derived from the fitted FoS curves. RESULTS: Sensitivity differences between the tasks varied widely (range = −11.3 dB to 21.6 dB) and did not correlate with visual field sensitivity nor whether the visual field location was in an area of steep sensitivity gradient within the visual field. Due to the wide variation in differences between the methods, there was no significant difference in mean sensitivity between the 2IFC task relative to the yes-no task, but a trend for higher sensitivity (mean = 1.9 dB, SD = 6.0 dB, P = 0.11). Response variability and maximum response probability did not differ between the tasks (P > 0.99 and 0.95, respectively). CONCLUSIONS: Perimetric sensitivity estimates are demonstrably altered by observer response criterion but the effect varies widely and unpredictably, even within a single test. Response bias should be considered a factor in perimetric test variability and when comparing sensitivities to nonperimetric data. TRANSLATIONAL RELEVANCE: The effect of response criterion on perimetric response variability varies widely and unpredictably, even within a single test. The Association for Research in Vision and Ophthalmology 2021-01-08 /pmc/articles/PMC7804569/ /pubmed/33510957 http://dx.doi.org/10.1167/tvst.10.1.18 Text en Copyright 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Article
Rubinstein, Nikki J.
Turpin, Andrew
Denniss, Jonathan
McKendrick, Allison M.
Effects of Criterion Bias on Perimetric Sensitivity and Response Variability in Glaucoma
title Effects of Criterion Bias on Perimetric Sensitivity and Response Variability in Glaucoma
title_full Effects of Criterion Bias on Perimetric Sensitivity and Response Variability in Glaucoma
title_fullStr Effects of Criterion Bias on Perimetric Sensitivity and Response Variability in Glaucoma
title_full_unstemmed Effects of Criterion Bias on Perimetric Sensitivity and Response Variability in Glaucoma
title_short Effects of Criterion Bias on Perimetric Sensitivity and Response Variability in Glaucoma
title_sort effects of criterion bias on perimetric sensitivity and response variability in glaucoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7804569/
https://www.ncbi.nlm.nih.gov/pubmed/33510957
http://dx.doi.org/10.1167/tvst.10.1.18
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