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Enhancing Multi-disease Diagnosis of Chest X-rays with Advanced Deep-learning Networks in Real-world Data

The current artificial intelligence (AI) models are still insufficient in multi-disease diagnosis for real-world data, which always present a long-tail distribution. To tackle this issue, a long-tail public dataset, “ChestX-ray14,” which involved fourteen (14) disease labels, was randomly divided in...

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Autores principales: Chen, Yuyang, Wan, Yiliang, Pan, Feng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054207/
https://www.ncbi.nlm.nih.gov/pubmed/36988837
http://dx.doi.org/10.1007/s10278-023-00801-4
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author Chen, Yuyang
Wan, Yiliang
Pan, Feng
author_facet Chen, Yuyang
Wan, Yiliang
Pan, Feng
author_sort Chen, Yuyang
collection PubMed
description The current artificial intelligence (AI) models are still insufficient in multi-disease diagnosis for real-world data, which always present a long-tail distribution. To tackle this issue, a long-tail public dataset, “ChestX-ray14,” which involved fourteen (14) disease labels, was randomly divided into the train, validation, and test sets with ratios of 0.7, 0.1, and 0.2. Two pretrained state-of-the-art networks, EfficientNet-b5 and CoAtNet-0-rw, were chosen as the backbones. After the fully-connected layer, a final layer of 14 sigmoid activation units was added to output each disease’s diagnosis. To achieve better adaptive learning, a novel loss (L(ours)) was designed, which coalesced reweighting and tail sample focus. For comparison, a pretrained ResNet50 network with weighted binary cross-entropy loss (L(WBCE)) was used as a baseline, which showed the best performance in a previous study. The overall and individual areas under the receiver operating curve (AUROC) for each disease label were evaluated and compared among different models. Group-score-weighted class activation mapping (Group-CAM) is applied for visual interpretations. As a result, the pretrained CoAtNet-0-rw + L(ours) showed the best overall AUROC of 0.842, significantly higher than ResNet50 + L(WBCE) (AUROC: 0.811, p = 0.037). Group-CAM presented that the model could pay the proper attention to lesions for most disease labels (e.g., atelectasis, edema, effusion) but wrong attention for the other labels, such as pneumothorax; meanwhile, mislabeling of the dataset was found. Overall, this study presented an advanced AI diagnostic model achieving a significant improvement in the multi-disease diagnosis of chest X-rays, particularly in real-world data with challenging long-tail distributions.
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spelling pubmed-100542072023-03-29 Enhancing Multi-disease Diagnosis of Chest X-rays with Advanced Deep-learning Networks in Real-world Data Chen, Yuyang Wan, Yiliang Pan, Feng J Digit Imaging Original Paper The current artificial intelligence (AI) models are still insufficient in multi-disease diagnosis for real-world data, which always present a long-tail distribution. To tackle this issue, a long-tail public dataset, “ChestX-ray14,” which involved fourteen (14) disease labels, was randomly divided into the train, validation, and test sets with ratios of 0.7, 0.1, and 0.2. Two pretrained state-of-the-art networks, EfficientNet-b5 and CoAtNet-0-rw, were chosen as the backbones. After the fully-connected layer, a final layer of 14 sigmoid activation units was added to output each disease’s diagnosis. To achieve better adaptive learning, a novel loss (L(ours)) was designed, which coalesced reweighting and tail sample focus. For comparison, a pretrained ResNet50 network with weighted binary cross-entropy loss (L(WBCE)) was used as a baseline, which showed the best performance in a previous study. The overall and individual areas under the receiver operating curve (AUROC) for each disease label were evaluated and compared among different models. Group-score-weighted class activation mapping (Group-CAM) is applied for visual interpretations. As a result, the pretrained CoAtNet-0-rw + L(ours) showed the best overall AUROC of 0.842, significantly higher than ResNet50 + L(WBCE) (AUROC: 0.811, p = 0.037). Group-CAM presented that the model could pay the proper attention to lesions for most disease labels (e.g., atelectasis, edema, effusion) but wrong attention for the other labels, such as pneumothorax; meanwhile, mislabeling of the dataset was found. Overall, this study presented an advanced AI diagnostic model achieving a significant improvement in the multi-disease diagnosis of chest X-rays, particularly in real-world data with challenging long-tail distributions. Springer International Publishing 2023-03-29 2023-08 /pmc/articles/PMC10054207/ /pubmed/36988837 http://dx.doi.org/10.1007/s10278-023-00801-4 Text en © The Author(s) under exclusive licence to Society for Imaging Informatics in Medicine 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
spellingShingle Original Paper
Chen, Yuyang
Wan, Yiliang
Pan, Feng
Enhancing Multi-disease Diagnosis of Chest X-rays with Advanced Deep-learning Networks in Real-world Data
title Enhancing Multi-disease Diagnosis of Chest X-rays with Advanced Deep-learning Networks in Real-world Data
title_full Enhancing Multi-disease Diagnosis of Chest X-rays with Advanced Deep-learning Networks in Real-world Data
title_fullStr Enhancing Multi-disease Diagnosis of Chest X-rays with Advanced Deep-learning Networks in Real-world Data
title_full_unstemmed Enhancing Multi-disease Diagnosis of Chest X-rays with Advanced Deep-learning Networks in Real-world Data
title_short Enhancing Multi-disease Diagnosis of Chest X-rays with Advanced Deep-learning Networks in Real-world Data
title_sort enhancing multi-disease diagnosis of chest x-rays with advanced deep-learning networks in real-world data
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10054207/
https://www.ncbi.nlm.nih.gov/pubmed/36988837
http://dx.doi.org/10.1007/s10278-023-00801-4
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