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Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning

PURPOSE: Optical coherence tomography (OCT) is widely used in the management of retinal pathologies, including age-related macular degeneration (AMD), diabetic macular edema (DME), and primary open-angle glaucoma (POAG). We used machine learning techniques to understand diagnostic performance gains...

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Autores principales: Lin, Andrew C., Lee, Cecilia S., Blazes, Marian, Lee, Aaron Y., Gorin, Michael B.
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/PMC8161701/
https://www.ncbi.nlm.nih.gov/pubmed/34038502
http://dx.doi.org/10.1167/tvst.10.6.32
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author Lin, Andrew C.
Lee, Cecilia S.
Blazes, Marian
Lee, Aaron Y.
Gorin, Michael B.
author_facet Lin, Andrew C.
Lee, Cecilia S.
Blazes, Marian
Lee, Aaron Y.
Gorin, Michael B.
author_sort Lin, Andrew C.
collection PubMed
description PURPOSE: Optical coherence tomography (OCT) is widely used in the management of retinal pathologies, including age-related macular degeneration (AMD), diabetic macular edema (DME), and primary open-angle glaucoma (POAG). We used machine learning techniques to understand diagnostic performance gains from expanding macular OCT B-scans compared with foveal-only OCT B-scans for these conditions. METHODS: Electronic medical records were extracted to obtain 61 B-scans per eye from patients with AMD, diabetic retinopathy, or POAG. We constructed deep neural networks and random forest ensembles and generated area under the receiver operating characteristic (AUROC) and area under the precision recall (AUPR) curves. RESULTS: After extracting 630,000 OCT images, we achieved improved AUROC and AUPR curves when comparing the central image (one B-scan) to all images (61 B-scans). The AUROC and AUPR points of diminishing return for diagnostic accuracy for macular OCT coverage were found to be within 2.75 to 4.00 mm (14–19 B-scans), 4.25 to 4.50 mm (20–21 B-scans), and 4.50 to 6.25 mm (21–28 B-scans) for AMD, DME, and POAG, respectively. All models with >0.25 mm of coverage had statistically significantly improved AUROC/AUPR curves for all diseases (P < 0.05). CONCLUSIONS: Systematically expanded macular coverage models demonstrated significant differences in total macular coverage required for improved diagnostic accuracy, with the largest macular area being relevant in POAG followed by DME and then AMD. These findings support our hypothesis that the extent of macular coverage by OCT imaging in the clinical setting, for any of the three major disorders, has a measurable impact on the functionality of artificial intelligence decision support. TRANSLATIONAL RELEVANCE: We used machine learning techniques to improve OCT imaging standards for common retinal disease diagnoses.
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spelling pubmed-81617012021-06-09 Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning Lin, Andrew C. Lee, Cecilia S. Blazes, Marian Lee, Aaron Y. Gorin, Michael B. Transl Vis Sci Technol Article PURPOSE: Optical coherence tomography (OCT) is widely used in the management of retinal pathologies, including age-related macular degeneration (AMD), diabetic macular edema (DME), and primary open-angle glaucoma (POAG). We used machine learning techniques to understand diagnostic performance gains from expanding macular OCT B-scans compared with foveal-only OCT B-scans for these conditions. METHODS: Electronic medical records were extracted to obtain 61 B-scans per eye from patients with AMD, diabetic retinopathy, or POAG. We constructed deep neural networks and random forest ensembles and generated area under the receiver operating characteristic (AUROC) and area under the precision recall (AUPR) curves. RESULTS: After extracting 630,000 OCT images, we achieved improved AUROC and AUPR curves when comparing the central image (one B-scan) to all images (61 B-scans). The AUROC and AUPR points of diminishing return for diagnostic accuracy for macular OCT coverage were found to be within 2.75 to 4.00 mm (14–19 B-scans), 4.25 to 4.50 mm (20–21 B-scans), and 4.50 to 6.25 mm (21–28 B-scans) for AMD, DME, and POAG, respectively. All models with >0.25 mm of coverage had statistically significantly improved AUROC/AUPR curves for all diseases (P < 0.05). CONCLUSIONS: Systematically expanded macular coverage models demonstrated significant differences in total macular coverage required for improved diagnostic accuracy, with the largest macular area being relevant in POAG followed by DME and then AMD. These findings support our hypothesis that the extent of macular coverage by OCT imaging in the clinical setting, for any of the three major disorders, has a measurable impact on the functionality of artificial intelligence decision support. TRANSLATIONAL RELEVANCE: We used machine learning techniques to improve OCT imaging standards for common retinal disease diagnoses. The Association for Research in Vision and Ophthalmology 2021-05-26 /pmc/articles/PMC8161701/ /pubmed/34038502 http://dx.doi.org/10.1167/tvst.10.6.32 Text en Copyright 2021 The Authors https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License.
spellingShingle Article
Lin, Andrew C.
Lee, Cecilia S.
Blazes, Marian
Lee, Aaron Y.
Gorin, Michael B.
Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning
title Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning
title_full Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning
title_fullStr Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning
title_full_unstemmed Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning
title_short Assessing the Clinical Utility of Expanded Macular OCTs Using Machine Learning
title_sort assessing the clinical utility of expanded macular octs using machine learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161701/
https://www.ncbi.nlm.nih.gov/pubmed/34038502
http://dx.doi.org/10.1167/tvst.10.6.32
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