用于多标签疾病诊断和解释的交叉和图像内原型学习

Chong Wang;Fengbei Liu;Yuanhong Chen;Helen Frazer;Gustavo Carneiro
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引用次数: 0

摘要

最近在原型学习方面的进展显示出了显著的潜力,它可以提供有用的决策解释,将激活图和预测与特定类别的训练原型联系起来。这种原型学习已经在各种单标签疾病中得到了很好的研究,但对于非常相关且更具挑战性的多标签诊断,其中多种疾病通常在图像中同时存在,现有的原型学习模型由于多种疾病的纠缠而难以获得有意义的激活图和有效的类原型。在本文中,我们提出了一个新的交叉和图像内原型学习(CIPL)框架,用于准确的多标签疾病诊断和医学图像解释。CIPL在学习原型时,利用常见的交叉图像语义来理清多种疾病,从而全面理解复杂的病理病变。此外,我们提出了一种新的基于两级对齐的正则化策略,该策略有效地利用一致的图像内信息来增强解释鲁棒性和预测性能。大量实验表明,我们的CIPL在两种疾病诊断的公共多标签基准(胸片和眼底图像)中达到了最先进的(SOTA)分类精度。定量可解释性结果表明,CIPL在弱监督胸椎疾病定位方面也优于其他主要的基于显著性和原型的解释方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cross- and Intra-Image Prototypical Learning for Multi-Label Disease Diagnosis and Interpretation
Recent advances in prototypical learning have shown remarkable potential to provide useful decision interpretations associating activation maps and predictions with class-specific training prototypes. Such prototypical learning has been well-studied for various single-label diseases, but for quite relevant and more challenging multi-label diagnosis, where multiple diseases are often concurrent within an image, existing prototypical learning models struggle to obtain meaningful activation maps and effective class prototypes due to the entanglement of the multiple diseases. In this paper, we present a novel Cross- and Intra-image Prototypical Learning (CIPL) framework, for accurate multi-label disease diagnosis and interpretation from medical images. CIPL takes advantage of common cross-image semantics to disentangle the multiple diseases when learning the prototypes, allowing a comprehensive understanding of complicated pathological lesions. Furthermore, we propose a new two-level alignment-based regularisation strategy that effectively leverages consistent intra-image information to enhance interpretation robustness and predictive performance. Extensive experiments show that our CIPL attains the state-of-the-art (SOTA) classification accuracy in two public multi-label benchmarks of disease diagnosis: thoracic radiography and fundus images. Quantitative interpretability results show that CIPL also has superiority in weakly-supervised thoracic disease localisation over other leading saliency- and prototype-based explanation methods.
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