Fangyao Tang1, Xi Wang2, An-Ran Ran1, Carmen K M Chan3, Mary Ho4,5, Wilson Yip4,5, Alvin L Young4,5, Jerry Lok3, Simon Szeto3, Jason Chan3, Fanny Yip3, Raymond Wong3, Ziqi Tang1, Dawei Yang1, Danny S Ng1,3, Li Jia Chen1,4, Marten Brelén1, Victor Chu6, Kenneth Li6, Tracy H T Lai6, Gavin S Tan7, Daniel S W Ting7, Haifan Huang8, Haoyu Chen8, Jacey Hongjie Ma9, Shibo Tang9, Theodore Leng10, Schahrouz Kakavand10, Suria S Mannil10, Robert T Chang10, Gerald Liew11, Bamini Gopinath11,12, Timothy Y Y Lai1, Chi Pui Pang1, Peter H Scanlon13, Tien Yin Wong7, Clement C Tham1,3,4, Hao Chen14, Pheng-Ann Heng2, Carol Y Cheung15. 1. Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong SAR. 2. Department of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR. 3. Hong Kong Eye Hospital, Hong Kong SAR. 4. Department of Ophthalmology and Visual Sciences, Prince of Wales Hospital, Hong Kong SAR. 5. Alice Ho Miu Ling Nethersole Hospital, Hong Kong SAR. 6. United Christian Hospital, Hong Kong SAR. 7. Singapore Eye Research Institute, Singapore National Eye Centre, Singapore. 8. Joint Shantou International Eye Center, Shantou University and The Chinese University of Hong Kong, Shantou, Guangdong, China. 9. Aier School of Ophthalmology, Central South University, Changsha, Hunan, China. 10. Byers Eye Institute at Stanford, Stanford University School of Medicine, Palo Alto, CA. 11. Department of Ophthalmology, Westmead Institute for Medical Research, University of Sydney, Sydney, NSW, Australia. 12. Macquarie University Hearing, Department of Linguistics, Macquarie University, Sydney, New South Wales, Australia. 13. Gloucestershire Retinal Research Group, Gloucestershire Hospitals NHS Foundation Trust, Gloucester, U.K. 14. Department of Computer Science and Engineering, The Hong Kong University of Sciences and Technology, Hong Kong SAR. 15. Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong SAR carolcheung@cuhk.edu.hk.
Abstract
OBJECTIVE: Diabetic macular edema (DME) is the primary cause of vision loss among individuals with diabetes mellitus (DM). We developed, validated, and tested a deep learning (DL) system for classifying DME using images from three common commercially available optical coherence tomography (OCT) devices. RESEARCH DESIGN AND METHODS: We trained and validated two versions of a multitask convolution neural network (CNN) to classify DME (center-involved DME [CI-DME], non-CI-DME, or absence of DME) using three-dimensional (3D) volume scans and 2D B-scans, respectively. For both 3D and 2D CNNs, we used the residual network (ResNet) as the backbone. For the 3D CNN, we used a 3D version of ResNet-34 with the last fully connected layer removed as the feature extraction module. A total of 73,746 OCT images were used for training and primary validation. External testing was performed using 26,981 images across seven independent data sets from Singapore, Hong Kong, the U.S., China, and Australia. RESULTS: In classifying the presence or absence of DME, the DL system achieved area under the receiver operating characteristic curves (AUROCs) of 0.937 (95% CI 0.920-0.954), 0.958 (0.930-0.977), and 0.965 (0.948-0.977) for the primary data set obtained from CIRRUS, SPECTRALIS, and Triton OCTs, respectively, in addition to AUROCs >0.906 for the external data sets. For further classification of the CI-DME and non-CI-DME subgroups, the AUROCs were 0.968 (0.940-0.995), 0.951 (0.898-0.982), and 0.975 (0.947-0.991) for the primary data set and >0.894 for the external data sets. CONCLUSIONS: We demonstrated excellent performance with a DL system for the automated classification of DME, highlighting its potential as a promising second-line screening tool for patients with DM, which may potentially create a more effective triaging mechanism to eye clinics.
OBJECTIVE: Diabetic macular edema (DME) is the primary cause of vision loss among individuals with diabetes mellitus (DM). We developed, validated, and tested a deep learning (DL) system for classifying DME using images from three common commercially available optical coherence tomography (OCT) devices. RESEARCH DESIGN AND METHODS: We trained and validated two versions of a multitask convolution neural network (CNN) to classify DME (center-involved DME [CI-DME], non-CI-DME, or absence of DME) using three-dimensional (3D) volume scans and 2D B-scans, respectively. For both 3D and 2D CNNs, we used the residual network (ResNet) as the backbone. For the 3D CNN, we used a 3D version of ResNet-34 with the last fully connected layer removed as the feature extraction module. A total of 73,746 OCT images were used for training and primary validation. External testing was performed using 26,981 images across seven independent data sets from Singapore, Hong Kong, the U.S., China, and Australia. RESULTS: In classifying the presence or absence of DME, the DL system achieved area under the receiver operating characteristic curves (AUROCs) of 0.937 (95% CI 0.920-0.954), 0.958 (0.930-0.977), and 0.965 (0.948-0.977) for the primary data set obtained from CIRRUS, SPECTRALIS, and Triton OCTs, respectively, in addition to AUROCs >0.906 for the external data sets. For further classification of the CI-DME and non-CI-DME subgroups, the AUROCs were 0.968 (0.940-0.995), 0.951 (0.898-0.982), and 0.975 (0.947-0.991) for the primary data set and >0.894 for the external data sets. CONCLUSIONS: We demonstrated excellent performance with a DL system for the automated classification of DME, highlighting its potential as a promising second-line screening tool for patients with DM, which may potentially create a more effective triaging mechanism to eye clinics.
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