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Automated retinopathy of prematurity screening using deep neural networks
BACKGROUND: Retinopathy of prematurity (ROP) is the leading cause of childhood blindness worldwide. Automated ROP detection system is urgent and it appears to be a safe, reliable, and cost-effective complement to human experts. METHODS: An automated ROP detection system called DeepROP was developed...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156692/ https://www.ncbi.nlm.nih.gov/pubmed/30166272 http://dx.doi.org/10.1016/j.ebiom.2018.08.033 |
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author | Wang, Jianyong Ju, Rong Chen, Yuanyuan Zhang, Lei Hu, Junjie Wu, Yu Dong, Wentao Zhong, Jie Yi, Zhang |
author_facet | Wang, Jianyong Ju, Rong Chen, Yuanyuan Zhang, Lei Hu, Junjie Wu, Yu Dong, Wentao Zhong, Jie Yi, Zhang |
author_sort | Wang, Jianyong |
collection | PubMed |
description | BACKGROUND: Retinopathy of prematurity (ROP) is the leading cause of childhood blindness worldwide. Automated ROP detection system is urgent and it appears to be a safe, reliable, and cost-effective complement to human experts. METHODS: An automated ROP detection system called DeepROP was developed by using Deep Neural Networks (DNNs). ROP detection was divided into ROP identification and grading tasks. Two specific DNN models, i.e., Id-Net and Gr-Net, were designed for identification and grading tasks, respectively. To develop the DNNs, large-scale datasets of retinal fundus images were constructed by labeling the images of ROP screenings by clinical ophthalmologists. FINDINGS: On the test dataset, the Id-Net achieved a sensitivity of 96.62%(95%CI, 92.29%–98.89%) and a specificity of 99.32% (95%CI, 96.29%–9.98%) for ROP identification while the Gr-Net attained sensitivity and specificity values of 88.46% (95%CI, 96.29%–99.98%) and 92.31% (95%CI, 81.46%–97.86%), respectively, on the ROP grading task. On another 552 cases, the developed DNNs outperformed some human experts. In a clinical setting, the sensitivity and specificity values of DeepROP for ROP identification were 84.91% (95%CI, 76.65%–91.12%) and 96.90% (95%CI, 95.49%–97.96%), respectively, whereas the corresponding measures for ROP grading were 93.33%(95%CI, 68.05%–99.83%) and 73.63%(95%CI, 68.05%–99.83%), respectively. INTERPRETATION: We constructed large-scale ROP datasets with adequate clinical labels and proposed novel DNN models. The DNN models can directly learn ROP features from big data. The developed DeepROP is potential to be an efficient and effective system for automated ROP screening. FUND: National Natural Science Foundation of China under Grant 61432012 and U1435213. |
format | Online Article Text |
id | pubmed-6156692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-61566922018-09-27 Automated retinopathy of prematurity screening using deep neural networks Wang, Jianyong Ju, Rong Chen, Yuanyuan Zhang, Lei Hu, Junjie Wu, Yu Dong, Wentao Zhong, Jie Yi, Zhang EBioMedicine Research paper BACKGROUND: Retinopathy of prematurity (ROP) is the leading cause of childhood blindness worldwide. Automated ROP detection system is urgent and it appears to be a safe, reliable, and cost-effective complement to human experts. METHODS: An automated ROP detection system called DeepROP was developed by using Deep Neural Networks (DNNs). ROP detection was divided into ROP identification and grading tasks. Two specific DNN models, i.e., Id-Net and Gr-Net, were designed for identification and grading tasks, respectively. To develop the DNNs, large-scale datasets of retinal fundus images were constructed by labeling the images of ROP screenings by clinical ophthalmologists. FINDINGS: On the test dataset, the Id-Net achieved a sensitivity of 96.62%(95%CI, 92.29%–98.89%) and a specificity of 99.32% (95%CI, 96.29%–9.98%) for ROP identification while the Gr-Net attained sensitivity and specificity values of 88.46% (95%CI, 96.29%–99.98%) and 92.31% (95%CI, 81.46%–97.86%), respectively, on the ROP grading task. On another 552 cases, the developed DNNs outperformed some human experts. In a clinical setting, the sensitivity and specificity values of DeepROP for ROP identification were 84.91% (95%CI, 76.65%–91.12%) and 96.90% (95%CI, 95.49%–97.96%), respectively, whereas the corresponding measures for ROP grading were 93.33%(95%CI, 68.05%–99.83%) and 73.63%(95%CI, 68.05%–99.83%), respectively. INTERPRETATION: We constructed large-scale ROP datasets with adequate clinical labels and proposed novel DNN models. The DNN models can directly learn ROP features from big data. The developed DeepROP is potential to be an efficient and effective system for automated ROP screening. FUND: National Natural Science Foundation of China under Grant 61432012 and U1435213. Elsevier 2018-08-27 /pmc/articles/PMC6156692/ /pubmed/30166272 http://dx.doi.org/10.1016/j.ebiom.2018.08.033 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research paper Wang, Jianyong Ju, Rong Chen, Yuanyuan Zhang, Lei Hu, Junjie Wu, Yu Dong, Wentao Zhong, Jie Yi, Zhang Automated retinopathy of prematurity screening using deep neural networks |
title | Automated retinopathy of prematurity screening using deep neural networks |
title_full | Automated retinopathy of prematurity screening using deep neural networks |
title_fullStr | Automated retinopathy of prematurity screening using deep neural networks |
title_full_unstemmed | Automated retinopathy of prematurity screening using deep neural networks |
title_short | Automated retinopathy of prematurity screening using deep neural networks |
title_sort | automated retinopathy of prematurity screening using deep neural networks |
topic | Research paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156692/ https://www.ncbi.nlm.nih.gov/pubmed/30166272 http://dx.doi.org/10.1016/j.ebiom.2018.08.033 |
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