AI Article Synopsis

  • Central serous chorioretinopathy (CSC) is a common eye condition that the study aimed to diagnose and differentiate between its chronic and acute forms using deep learning from optical coherence tomography (OCT) images.
  • The developed model achieved high diagnostic performance with an accuracy of 93.8% for CSC and 97.6% for distinguishing its forms, closely matching or surpassing human ophthalmologists' diagnoses.
  • The findings suggest that automated deep learning systems could effectively assist in diagnosing CSC, potentially providing an independent tool alongside human experts.

Article Abstract

Central serous chorioretinopathy (CSC) is a common condition characterized by serous detachment of the neurosensory retina at the posterior pole. We built a deep learning system model to diagnose CSC, and distinguish chronic from acute CSC using spectral domain optical coherence tomography (SD-OCT) images. Data from SD-OCT images of patients with CSC and a control group were analyzed with a convolutional neural network. Sensitivity, specificity, accuracy, and area under the receiver operating characteristic curve (AUROC) were used to evaluate the model. For CSC diagnosis, our model showed an accuracy, sensitivity, and specificity of 93.8%, 90.0%, and 99.1%, respectively; AUROC was 98.9% (95% CI, 0.983-0.995); and its diagnostic performance was comparable with VGG-16, Resnet-50, and the diagnoses of five different ophthalmologists. For distinguishing chronic from acute cases, the accuracy, sensitivity, and specificity were 97.6%, 100.0%, and 92.6%, respectively; AUROC was 99.4% (95% CI, 0.985-1.000); performance was better than VGG-16 and Resnet-50, and was as good as the ophthalmologists. Our model performed well when diagnosing CSC and yielded highly accurate results when distinguishing between acute and chronic cases. Thus, automated deep learning system algorithms could play a role independent of human experts in the diagnosis of CSC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608618PMC
http://dx.doi.org/10.1038/s41598-020-75816-wDOI Listing

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