Prediction of Arteriovenous Access Dysfunction by Mel Spectrogram-based Deep Learning Model

光谱图 深度学习 计算机科学 医学 人工智能 心脏病学
作者
Tung‐Ling Chung,Yi‐Hsueh Liu,Pei-Yu Wu,Jiun‐Chi Huang,Yi-Chun Tsai,Yuchen Wang,Shan-Pin Pan,Ya‐Ling Hsu,Szu‐Chia Chen
出处
期刊:International Journal of Medical Sciences [Ivyspring International Publisher]
卷期号:21 (12): 2252-2260 被引量:4
标识
DOI:10.7150/ijms.98421
摘要

Background: The early detection of arteriovenous (AV) access dysfunction is crucial for maintaining the patency of vascular access. This study aimed to use deep learning to predict AV access malfunction necessitating further vascular management. Methods: This prospective cohort study enrolled prevalent hemodialysis (HD) patients with an AV fistula or AV graft from a single HD center. Their AV access bruit sounds were recorded weekly using an electronic stethoscope from three different sites (arterial needle site, venous needle site, and the midpoint between the arterial and venous needle sites) before HD sessions. The audio signals were converted to Mel spectrograms using Fourier transformation and utilized to develop deep learning models. Three deep learning models, (1) Convolutional Neural Network (CNN), (2) Convolutional Recurrent Neural Network (CRNN), and (3) Vision Transformers-Gate Recurrent Unit (ViT-GRU), were trained and compared to predict the likelihood of dysfunctional AV access. Results: Total 437 audio recordings were obtained from 84 patients. The CNN model outperformed the other models in the test set, with an F1 score of 0.7037 and area under the receiver operating characteristic curve (AUROC) of 0.7112. The Vit-GRU model had high performance in out-of-fold predictions, with an F1 score of 0.7131 and AUROC of 0.7745, but low generalization ability in the test set, with an F1 score of 0.5225 and AUROC of 0.5977. Conclusions: The CNN model based on Mel spectrograms could predict malfunctioning AV access requiring vascular intervention within 10 days. This approach could serve as a useful screening tool for high-risk AV access.
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