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Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting

PURPOSE: This study aims to meet a growing need for a fully automated, learning-based interpretation tool for retinal images obtained remotely (e.g. teleophthalmology) through different imaging modalities that may include imperfect (uninterpretable) images. METHODS: A retrospective study of 1148 opt...

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Autores principales: Gao, Qitong, Amason, Joshua, Cousins, Scott, Pajic, Miroslav, Hadziahmetovic, Majda
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/PMC8161696/
https://www.ncbi.nlm.nih.gov/pubmed/34036304
http://dx.doi.org/10.1167/tvst.10.6.30
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author Gao, Qitong
Amason, Joshua
Cousins, Scott
Pajic, Miroslav
Hadziahmetovic, Majda
author_facet Gao, Qitong
Amason, Joshua
Cousins, Scott
Pajic, Miroslav
Hadziahmetovic, Majda
author_sort Gao, Qitong
collection PubMed
description PURPOSE: This study aims to meet a growing need for a fully automated, learning-based interpretation tool for retinal images obtained remotely (e.g. teleophthalmology) through different imaging modalities that may include imperfect (uninterpretable) images. METHODS: A retrospective study of 1148 optical coherence tomography (OCT) and color fundus photography (CFP) retinal images obtained using Topcon's Maestro care unit on 647 patients with diabetes. To identify retinal pathology, a Convolutional Neural Network (CNN) with dual-modal inputs (i.e. CFP and OCT images) was developed. We developed a novel alternate gradient descent algorithm to train the CNN, which allows for the use of uninterpretable CFP/OCT images (i.e. ungradable images that do not contain sufficient image biomarkers for the reviewer to conclude absence or presence of retinal pathology). Specifically, a 9:1 ratio to split the training and testing dataset was used for training and validating the CNN. Paired CFP/OCT inputs (obtained from a single eye of a patient) were grouped as retinal pathology negative (RPN; 924 images) in the absence of retinal pathology in both imaging modalities, or if one of the imaging modalities was uninterpretable and the other without retinal pathology. If any imaging modality exhibited referable retinal pathology, the corresponding CFP/OCT inputs were deemed retinal pathology positive (RPP; 224 images) if any imaging modality exhibited referable retinal pathology. RESULTS: Our approach achieved 88.60% (95% confidence interval [CI] = 82.76% to 94.43%) accuracy in identifying pathology, along with the false negative rate (FNR) of 12.28% (95% CI = 6.26% to 18.31%), recall (sensitivity) of 87.72% (95% CI = 81.69% to 93.74%), specificity of 89.47% (95% CI = 83.84% to 95.11%), and area under the curve of receiver operating characteristic (AUC-ROC) was 92.74% (95% CI = 87.71% to 97.76%). CONCLUSIONS: Our model can be successfully deployed in clinical practice to facilitate automated remote retinal pathology identification. TRANSLATIONAL RELEVANCE: A fully automated tool for early diagnosis of retinal pathology might allow for earlier treatment and improved visual outcomes.
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spelling pubmed-81616962021-06-09 Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting Gao, Qitong Amason, Joshua Cousins, Scott Pajic, Miroslav Hadziahmetovic, Majda Transl Vis Sci Technol Article PURPOSE: This study aims to meet a growing need for a fully automated, learning-based interpretation tool for retinal images obtained remotely (e.g. teleophthalmology) through different imaging modalities that may include imperfect (uninterpretable) images. METHODS: A retrospective study of 1148 optical coherence tomography (OCT) and color fundus photography (CFP) retinal images obtained using Topcon's Maestro care unit on 647 patients with diabetes. To identify retinal pathology, a Convolutional Neural Network (CNN) with dual-modal inputs (i.e. CFP and OCT images) was developed. We developed a novel alternate gradient descent algorithm to train the CNN, which allows for the use of uninterpretable CFP/OCT images (i.e. ungradable images that do not contain sufficient image biomarkers for the reviewer to conclude absence or presence of retinal pathology). Specifically, a 9:1 ratio to split the training and testing dataset was used for training and validating the CNN. Paired CFP/OCT inputs (obtained from a single eye of a patient) were grouped as retinal pathology negative (RPN; 924 images) in the absence of retinal pathology in both imaging modalities, or if one of the imaging modalities was uninterpretable and the other without retinal pathology. If any imaging modality exhibited referable retinal pathology, the corresponding CFP/OCT inputs were deemed retinal pathology positive (RPP; 224 images) if any imaging modality exhibited referable retinal pathology. RESULTS: Our approach achieved 88.60% (95% confidence interval [CI] = 82.76% to 94.43%) accuracy in identifying pathology, along with the false negative rate (FNR) of 12.28% (95% CI = 6.26% to 18.31%), recall (sensitivity) of 87.72% (95% CI = 81.69% to 93.74%), specificity of 89.47% (95% CI = 83.84% to 95.11%), and area under the curve of receiver operating characteristic (AUC-ROC) was 92.74% (95% CI = 87.71% to 97.76%). CONCLUSIONS: Our model can be successfully deployed in clinical practice to facilitate automated remote retinal pathology identification. TRANSLATIONAL RELEVANCE: A fully automated tool for early diagnosis of retinal pathology might allow for earlier treatment and improved visual outcomes. The Association for Research in Vision and Ophthalmology 2021-05-25 /pmc/articles/PMC8161696/ /pubmed/34036304 http://dx.doi.org/10.1167/tvst.10.6.30 Text en Copyright 2021 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 Article
Gao, Qitong
Amason, Joshua
Cousins, Scott
Pajic, Miroslav
Hadziahmetovic, Majda
Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting
title Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting
title_full Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting
title_fullStr Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting
title_full_unstemmed Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting
title_short Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting
title_sort automated identification of referable retinal pathology in teleophthalmology setting
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161696/
https://www.ncbi.nlm.nih.gov/pubmed/34036304
http://dx.doi.org/10.1167/tvst.10.6.30
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