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Automated Multi-Lesion Detection for Referable Diabetic Retinopathy in Indigenous Health Care
Diabetic Retinopathy (DR) is a complication of diabetes mellitus that affects more than one-quarter of the population with diabetes, and can lead to blindness if not discovered in time. An automated screening enables the identification of patients who need further medical attention. This study aimed...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452786/ https://www.ncbi.nlm.nih.gov/pubmed/26035836 http://dx.doi.org/10.1371/journal.pone.0127664 |
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author | Pires, Ramon Carvalho, Tiago Spurling, Geoffrey Goldenstein, Siome Wainer, Jacques Luckie, Alan Jelinek, Herbert F. Rocha, Anderson |
author_facet | Pires, Ramon Carvalho, Tiago Spurling, Geoffrey Goldenstein, Siome Wainer, Jacques Luckie, Alan Jelinek, Herbert F. Rocha, Anderson |
author_sort | Pires, Ramon |
collection | PubMed |
description | Diabetic Retinopathy (DR) is a complication of diabetes mellitus that affects more than one-quarter of the population with diabetes, and can lead to blindness if not discovered in time. An automated screening enables the identification of patients who need further medical attention. This study aimed to classify retinal images of Aboriginal and Torres Strait Islander peoples utilizing an automated computer-based multi-lesion eye screening program for diabetic retinopathy. The multi-lesion classifier was trained on 1,014 images from the São Paulo Eye Hospital and tested on retinal images containing no DR-related lesion, single lesions, or multiple types of lesions from the Inala Aboriginal and Torres Strait Islander health care centre. The automated multi-lesion classifier has the potential to enhance the efficiency of clinical practice delivering diabetic retinopathy screening. Our program does not necessitate image samples for training from any specific ethnic group or population being assessed and is independent of image pre- or post-processing to identify retinal lesions. In this Aboriginal and Torres Strait Islander population, the program achieved 100% sensitivity and 88.9% specificity in identifying bright lesions, while detection of red lesions achieved a sensitivity of 67% and specificity of 95%. When both bright and red lesions were present, 100% sensitivity with 88.9% specificity was obtained. All results obtained with this automated screening program meet WHO standards for diabetic retinopathy screening. |
format | Online Article Text |
id | pubmed-4452786 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44527862015-06-09 Automated Multi-Lesion Detection for Referable Diabetic Retinopathy in Indigenous Health Care Pires, Ramon Carvalho, Tiago Spurling, Geoffrey Goldenstein, Siome Wainer, Jacques Luckie, Alan Jelinek, Herbert F. Rocha, Anderson PLoS One Research Article Diabetic Retinopathy (DR) is a complication of diabetes mellitus that affects more than one-quarter of the population with diabetes, and can lead to blindness if not discovered in time. An automated screening enables the identification of patients who need further medical attention. This study aimed to classify retinal images of Aboriginal and Torres Strait Islander peoples utilizing an automated computer-based multi-lesion eye screening program for diabetic retinopathy. The multi-lesion classifier was trained on 1,014 images from the São Paulo Eye Hospital and tested on retinal images containing no DR-related lesion, single lesions, or multiple types of lesions from the Inala Aboriginal and Torres Strait Islander health care centre. The automated multi-lesion classifier has the potential to enhance the efficiency of clinical practice delivering diabetic retinopathy screening. Our program does not necessitate image samples for training from any specific ethnic group or population being assessed and is independent of image pre- or post-processing to identify retinal lesions. In this Aboriginal and Torres Strait Islander population, the program achieved 100% sensitivity and 88.9% specificity in identifying bright lesions, while detection of red lesions achieved a sensitivity of 67% and specificity of 95%. When both bright and red lesions were present, 100% sensitivity with 88.9% specificity was obtained. All results obtained with this automated screening program meet WHO standards for diabetic retinopathy screening. Public Library of Science 2015-06-02 /pmc/articles/PMC4452786/ /pubmed/26035836 http://dx.doi.org/10.1371/journal.pone.0127664 Text en © 2015 Pires et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Pires, Ramon Carvalho, Tiago Spurling, Geoffrey Goldenstein, Siome Wainer, Jacques Luckie, Alan Jelinek, Herbert F. Rocha, Anderson Automated Multi-Lesion Detection for Referable Diabetic Retinopathy in Indigenous Health Care |
title | Automated Multi-Lesion Detection for Referable Diabetic Retinopathy in Indigenous Health Care |
title_full | Automated Multi-Lesion Detection for Referable Diabetic Retinopathy in Indigenous Health Care |
title_fullStr | Automated Multi-Lesion Detection for Referable Diabetic Retinopathy in Indigenous Health Care |
title_full_unstemmed | Automated Multi-Lesion Detection for Referable Diabetic Retinopathy in Indigenous Health Care |
title_short | Automated Multi-Lesion Detection for Referable Diabetic Retinopathy in Indigenous Health Care |
title_sort | automated multi-lesion detection for referable diabetic retinopathy in indigenous health care |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4452786/ https://www.ncbi.nlm.nih.gov/pubmed/26035836 http://dx.doi.org/10.1371/journal.pone.0127664 |
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