Evidence map›Paper›PMID 41367772›Full record

ArticleQuantitative imaging in medicine and surgery2025

Early identification of abnormal pulmonary infectious diseases using unsupervised anomaly detection.

Rong Liu, Yuhe Zhu, Zhangwen Lyu, Yite Gao, Yinwei Zhan, Yuefu Zhan

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Article in Quantitative imaging in medicine and surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Rong LiuSchool of Computer Science and Technology, Guangdong University of Technology, Guangzhou, China.
Yuhe ZhuSchool of Computer Science and Technology, Guangdong University of Technology, Guangzhou, China.
Zhangwen LyuSchool of Computer Science and Technology, Guangdong University of Technology, Guangzhou, China.
Yite GaoSchool of Computer Science and Technology, Guangdong University of Technology, Guangzhou, China.
Yinwei ZhanSchool of Computer Science and Technology, Guangdong University of Technology, Guangzhou, China.
Yuefu ZhanDepartment of Radiology, The Third People's Hospital of Longgang, Clinical Institute of Shantou University Medical College (The Third People's Hospital of Longgang District Shenzhen), Shenzhen, China.

Funding

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6 · The paper itself

Abstract

Background: The early identification of abnormal pulmonary infectious diseases (APIDs) could effectively control the large-scale spread of such diseases. This study proposed a deep learning-based method for the early identification of APIDs. Methods: Unsupervised anomaly detection (UAD) refers to the identification of abnormal samples of which its distribution differs from that of normal samples using a training set comprised of only normal samples. Building on this principle, we proposed a method for the early identification of APIDs. First, we established a pulmonary infection computed tomography (PICT) image sequence dataset, which included computed tomography (CT) image sequences of various common pulmonary infections, as well as two known abnormal cases [coronavirus disease 2019 (COVID-19) and melioidosis pneumonia]. Under our framework, only common infection sequences were used to train the UAD network, while both common and abnormal sequences were used in testing to assess the capability of the network to identify deviations. This approach not only detected the two known abnormal cases but was also able to detect unknown APIDs. To enhance the detection accuracy (ACC) of our approach, we developed the local reconstruction autoencoder (LRAE), which focuses on local regions in PICT images to effectively distinguish between common and abnormal infection areas. Results: Comprehensive experiments on the PICT dataset were conducted using metrics such as the area under the curve (AUC), F1-score, and ACC, and the results revealed the effectiveness and superiority of the LRAE compared to existing UAD methods. Specifically, the AUC, F1-score, and ACC of the LRAE in detecting COVID-19 CT image sequences were 0.8269, 0.7242, and 0.7801, respectively; while those for the melioidosis pneumonia CT image sequences were 0.8716, 0.6415, and 0.8146, respectively. Conclusions: This work offers a robust solution for the early identification of both known and emerging APIDs. The developed LRAE showed remarkable performance in detecting abnormal PICT image sequences.

Indexed as

abnormal pulmonary infectious diseases (APIDs)computed tomography image sequences (CT image sequences)deep learningEarly identificationunsupervised anomaly detection (UAD)

Identifiers

PMID41367772
PMCPMC12682555

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