Automated Identification of Referable Retinal Pathology in Teleophthalmology Setting

被引:4
作者
Gao, Qitong [1 ]
Amason, Joshua [2 ]
Cousins, Scott [2 ]
Pajic, Miroslav [1 ,3 ]
Hadziahmetovic, Majda [2 ]
机构
[1] Duke Univ, Dept Elect & Comp Engn, Durham, NC 27710 USA
[2] Duke Univ, Dept Ophthalmol, 2351 Erwin Rd, Durham, NC 27710 USA
[3] Duke Univ, Dept Comp Sci, Durham, NC 27710 USA
关键词
deep learning; automated diagnosis; retinal pathology; image analysis; teleophthalmology; DIABETIC-RETINOPATHY; MACULAR DEGENERATION; DEEP;
D O I
10.1167/tvst.10.6.30
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: This study aims to meet a growing need for a fully automated, learningbased 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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页数:12
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