Automated quantification of SARS-CoV-2 pneumonia with large vision model knowledge adaptation
Large vision models (LVM) pretrained by large datasets have demonstrated their enormous capacity to understand visual patterns and capture semantic information from images. We proposed a novel method of knowledge domain adaptation with pretrained LVM for a low-cost artificial intelligence (AI) model...
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Published in | New microbes and new infections Vol. 62; p. 101457 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.12.2024
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Large vision models (LVM) pretrained by large datasets have demonstrated their enormous capacity to understand visual patterns and capture semantic information from images. We proposed a novel method of knowledge domain adaptation with pretrained LVM for a low-cost artificial intelligence (AI) model to quantify the severity of SARS-CoV-2 pneumonia based on frontal chest X-ray (CXR) images.
Our method used the pretrained LVMs as the primary feature extractor and self-supervised contrastive learning for domain adaptation. An encoder with a 2048-dimensional feature vector output was first trained by self-supervised learning for knowledge domain adaptation. Then a multi-layer perceptron (MLP) was trained for the final severity prediction. A dataset with 2599 CXR images was used for model training and evaluation.
The model based on the pretrained vision transformer (ViT) and self-supervised learning achieved the best performance in cross validation, with mean squared error (MSE) of 23.83 (95 % CI 22.67–25.00) and mean absolute error (MAE) of 3.64 (95 % CI 3.54–3.73). Its prediction correlation has the R2 of 0.81 (95 % CI 0.79–0.82) and Spearman ρ of 0.80 (95 % CI 0.77–0.81), which are comparable to the current state-of-the-art (SOTA) methods trained by much larger CXR datasets.
The proposed new method has achieved the SOTA performance to quantify the severity of SARS-CoV-2 pneumonia at a significantly lower cost. The method can be extended to other infectious disease detection or quantification to expedite the application of AI in medical research. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Postal address: Building 38A, 8600 Rockville Pike MSC 6075 Bethesda, MD 20894, USA. |
ISSN: | 2052-2975 2052-2975 |
DOI: | 10.1016/j.nmni.2024.101457 |