A Trusted Lesion-assessment Network for Interpretable Diagnosis of Coronary Artery Disease in Coronary CT Angiography

Coronary Artery Disease (CAD) poses a significant threat to cardiovascular patients worldwide, underscoring the critical importance of automated CAD diagnostic technologies in clinical practice. Previous technologies for lesion assessment in Coronary CT Angiography (CCTA) images have been insufficient in terms of interpretability, resulting in solutions that lack clinical reliability in both network architecture and prediction outcomes, even when diagnoses are accurate. To address the limitation of interpretability, we introduce the Trusted Lesion-Assessment Network (TLA-Net), which provides a clinically reliable solution for multi-view CAD diagnosis: (1) The causality-informed evidence collection constructs a causal graph for the diagnostic process and implements causal interventions, preventing confounders' interference and enhancing the transparency of the network architecture. (2) The clinically-aligned uncertainty integration hierarchically combines Dirichlet distributions from various views based on clinical priors, offering confidence coefficients for prediction outcomes that align with physicians' image analysis procedures. Experimental results on a dataset of 2,618 lesions demonstrate that TLA-Net, supported by its interpretable methodological design, exhibits superior performance with outstanding generalization, domain adaptability, and robustness.

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Publication Details

Journal
Proceedings of the AAAI Conference on Artificial Intelligence
Published
2025-04-11
DOI
https://doi.org/10.1609/aaai.v39i6.32642
Citations
3
Primary Topic
Cardiac Imaging and Diagnostics
Type
article
Field-Weighted Citation Impact
3.18

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article

A Trusted Lesion-assessment Network for Interpretable Diagnosis of Coronary Artery Disease in Coronary CT Angiography

Zhaowen Qiu, Kuanquan Wang, Xinghua Ma, Xinyan Fang et al.
3 citations
Proceedings of the AAAI Conference on Artificial Intelligence
Cardiac Imaging and Diagnostics
3.18
article

A Trusted Lesion-assessment Network for Interpretable Diagnosis of Coronary Artery Disease in Coronary CT Angiography

Zhaowen Qiu, Kuanquan Wang, Xinghua Ma, Xinyan Fang, Gongning Luo, Shuo Li, Wei Wang, Mingye Zou, Xin Gao
article en
3 citations

Abstract

Coronary Artery Disease (CAD) poses a significant threat to cardiovascular patients worldwide, underscoring the critical importance of automated CAD diagnostic technologies in clinical practice. Previous technologies for lesion assessment in Coronary CT Angiography (CCTA) images have been insufficient in terms of interpretability, resulting in solutions that lack clinical reliability in both network architecture and prediction outcomes, even when diagnoses are accurate. To address the limitation of interpretability, we introduce the Trusted Lesion-Assessment Network (TLA-Net), which provides a clinically reliable solution for multi-view CAD diagnosis: (1) The causality-informed evidence collection constructs a causal graph for the diagnostic process and implements causal interventions, preventing confounders' interference and enhancing the transparency of the network architecture. (2) The clinically-aligned uncertainty integration hierarchically combines Dirichlet distributions from various views based on clinical priors, offering confidence coefficients for prediction outcomes that align with physicians' image analysis procedures. Experimental results on a dataset of 2,618 lesions demonstrate that TLA-Net, supported by its interpretable methodological design, exhibits superior performance with outstanding generalization, domain adaptability, and robustness.

Proceedings of the AAAI Conference on Artificial IntelligenceVol. 39(6)
Harbin Institute of Technology (CN), Northeast Forestry University (CN), Case Western Reserve University (US), King Abdullah University of Science and Technology (SA)
National Natural Science Foundation of China, King Abdullah University of Science and Technology
Openalex Percentile: Top 14%
Cardiac Imaging and Diagnostics
3.18
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