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A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma

PURPOSE: To develop a simulation model for glaucomatous longitudinal visual field (VF) tests with controlled progression rates. METHODS: Longitudinal VF tests of 1008 eyes from 755 patients with glaucoma were used to learn the statistical characteristics of VF progression. The learned statistics and...

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Autores principales: Li, Yan, Eizenman, Moshe, Shi, Runjie B., Buys, Yvonne M., Trope, Graham E., Wong, Willy
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/PMC10318593/
https://www.ncbi.nlm.nih.gov/pubmed/37382576
http://dx.doi.org/10.1167/tvst.12.6.27
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author Li, Yan
Eizenman, Moshe
Shi, Runjie B.
Buys, Yvonne M.
Trope, Graham E.
Wong, Willy
author_facet Li, Yan
Eizenman, Moshe
Shi, Runjie B.
Buys, Yvonne M.
Trope, Graham E.
Wong, Willy
author_sort Li, Yan
collection PubMed
description PURPOSE: To develop a simulation model for glaucomatous longitudinal visual field (VF) tests with controlled progression rates. METHODS: Longitudinal VF tests of 1008 eyes from 755 patients with glaucoma were used to learn the statistical characteristics of VF progression. The learned statistics and known anatomic correlations between VF test points were used to automatically generate progression patterns for baseline fields of patients with glaucoma. VF sequences were constructed by adding spatially correlated noise templates to the generated progression patterns. The two one-sided test (TOST) procedure was used to analyze the equivalence between simulated data and data from patients with glaucoma. VF progression detection rates in the simulated VF data were compared to those in patients with glaucoma using mean deviation (MD), cluster, and pointwise trend analysis. RESULTS: VF indices (MD, pattern standard deviation), MD linear regression slopes, and progression detection rates for the simulated and patients’ data were practically equivalent (TOST P < 0.01). In patients with glaucoma, the detection rates in 7 years using MD, cluster, and pointwise trend analysis were 24.4%, 26.2%, and 38.4%, respectively. In the simulated data, the mean detection rates (95% confidence interval) for MD, cluster, and pointwise trend analysis were 24.7% (24.1%–25.2%), 24.9% (24.2%–25.5%), and 35.7% (34.9%–36.5%), respectively. CONCLUSIONS: A novel simulation model generates glaucomatous VF sequences that are practically equivalent to longitudinal VFs from patients with glaucoma. TRANSLATIONAL RELEVANCE: Simulated VF sequences with controlled progression rates can support the evaluation and optimization of methods to detect VF progression and can provide guidance for the interpretation of longitudinal VFs.
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spelling pubmed-103185932023-07-05 A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma Li, Yan Eizenman, Moshe Shi, Runjie B. Buys, Yvonne M. Trope, Graham E. Wong, Willy Transl Vis Sci Technol Glaucoma PURPOSE: To develop a simulation model for glaucomatous longitudinal visual field (VF) tests with controlled progression rates. METHODS: Longitudinal VF tests of 1008 eyes from 755 patients with glaucoma were used to learn the statistical characteristics of VF progression. The learned statistics and known anatomic correlations between VF test points were used to automatically generate progression patterns for baseline fields of patients with glaucoma. VF sequences were constructed by adding spatially correlated noise templates to the generated progression patterns. The two one-sided test (TOST) procedure was used to analyze the equivalence between simulated data and data from patients with glaucoma. VF progression detection rates in the simulated VF data were compared to those in patients with glaucoma using mean deviation (MD), cluster, and pointwise trend analysis. RESULTS: VF indices (MD, pattern standard deviation), MD linear regression slopes, and progression detection rates for the simulated and patients’ data were practically equivalent (TOST P < 0.01). In patients with glaucoma, the detection rates in 7 years using MD, cluster, and pointwise trend analysis were 24.4%, 26.2%, and 38.4%, respectively. In the simulated data, the mean detection rates (95% confidence interval) for MD, cluster, and pointwise trend analysis were 24.7% (24.1%–25.2%), 24.9% (24.2%–25.5%), and 35.7% (34.9%–36.5%), respectively. CONCLUSIONS: A novel simulation model generates glaucomatous VF sequences that are practically equivalent to longitudinal VFs from patients with glaucoma. TRANSLATIONAL RELEVANCE: Simulated VF sequences with controlled progression rates can support the evaluation and optimization of methods to detect VF progression and can provide guidance for the interpretation of longitudinal VFs. The Association for Research in Vision and Ophthalmology 2023-06-29 /pmc/articles/PMC10318593/ /pubmed/37382576 http://dx.doi.org/10.1167/tvst.12.6.27 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 Glaucoma
Li, Yan
Eizenman, Moshe
Shi, Runjie B.
Buys, Yvonne M.
Trope, Graham E.
Wong, Willy
A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma
title A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma
title_full A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma
title_fullStr A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma
title_full_unstemmed A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma
title_short A Data-Driven Model for Simulating Longitudinal Visual Field Tests in Glaucoma
title_sort data-driven model for simulating longitudinal visual field tests in glaucoma
topic Glaucoma
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318593/
https://www.ncbi.nlm.nih.gov/pubmed/37382576
http://dx.doi.org/10.1167/tvst.12.6.27
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