AI Article Synopsis

  • - Diabetic retinopathy (DR) is a significant complication of diabetes that can lead to irreversible blindness, making early diagnosis through automatic grading essential for preventing vision loss in patients.
  • - Current DR grading models usually rely on single-field fundus images, which can't capture the entire retina and often miss important lesion details due to variability in appearance and location.
  • - A new multi-view DR grading framework has been developed, which uses images from multiple fields of view along with lesion snapshots to improve the model's ability to identify lesions, demonstrating better performance than previous methods in experiments on a large-scale dataset.

Article Abstract

As the most common complication of diabetes, diabetic retinopathy (DR) is one of the main causes of irreversible blindness. Automatic DR grading plays a crucial role in early diagnosis and intervention, reducing the risk of vision loss in people with diabetes. In these years, various deep-learning approaches for DR grading have been proposed. Most previous DR grading models are trained using the dataset of single-field fundus images, but the entire retina cannot be fully visualized in a single field of view. There are also problems of scattered location and great differences in the appearance of lesions in fundus images. To address the limitations caused by incomplete fundus features, and the difficulty in obtaining lesion information. This work introduces a novel multi-view DR grading framework, which solves the problem of incomplete fundus features by jointly learning fundus images from multiple fields of view. Furthermore, the proposed model combines multi-view inputs such as fundus images and lesion snapshots. It utilizes heterogeneous convolution blocks (HCB) and scalable self-attention classes (SSAC), which enhance the ability of the model to obtain lesion information. The experimental results show that our proposed method performs better than the benchmark methods on the large-scale dataset.

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http://dx.doi.org/10.1109/JBHI.2024.3384251DOI Listing

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