Evidence map›Paper›PMID 41061017›Full record

ArticlePLOS digital health2025

A lightweight deep neural network for personalized detecting ventricular arrhythmias from a single-lead ECG device.

Zhejun Sun, Wenrui Zhang, Yuxi Zhou, Shijia Geng, Deyun Zhang, Jiaze Wang, Bin Liu, Zhaoji Fu, Linlin Zheng, Chenyang Jiang and 2 more

Abstract read
In one paragraph

Article in PLOS digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Zhejun SunDepartment of Computer Science, Tianjin University of Technology, Tianjin, China.ORCID https://orcid.org/0009-0000-9836-407X
Wenrui ZhangNational Institute of Health Data Science, Peking University, Beijing, China.
Yuxi ZhouDepartment of Computer Science, Tianjin University of Technology, Tianjin, China.
Shijia GengHeartVoice Medical Technology, Hefei, China.
Deyun ZhangHeartVoice Medical Technology, Hefei, China.
Jiaze WangDepartment of Computer Science, Tianjin University of Technology, Tianjin, China.
Bin LiuDepartment of Computer Science, Tianjin University of Technology, Tianjin, China.
Zhaoji FuHeartVoice Medical Technology, Hefei, China.
Linlin ZhengDepartment of Electrocardiography, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Chenyang JiangDepartment of Cardiology, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Guigang ZhangInstitute of Automation, Chinese Academy of Sciences, Beijing, China.
Shenda HongNational Institute of Health Data Science, Peking University, Beijing, China.ORCID https://orcid.org/0000-0001-7521-5127

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ventricular arrhythmia (VA) is a leading cause of sudden cardiac death. Detecting VA from electrocardiograms (ECGs) using deep learning techniques has potential to improve clinical outcomes. However, developing robust deep learning models for ECG analysis remains challenging due to: (1) inter-subject diversity among different individuals, and (2) intra-subject diversity within the same subject across different physiological state over time. In this study, we address these challenges by introducing enhancements in both the pre-training and fine-tuning stages. In the pre-training stage, we propose a novel approach combining model-agnostic meta-learning (MAML) with curriculum learning (CL) to effectively address inter-subject diversity. MAML efficiently transfer knowledge from large-scale datasets and enables rapid model adaptation to new individuals using limited records. Integrating CL further enhances the effectiveness of MAML by sequentially training models from simpler to more complex tasks. For the fine-tuning stage, we propose an improved pre-fine-tuning strategy specifically designed to manage the intra-subject diversity. We evaluate our methods on three publicly available ECG datasets and one real-world clinical ECG dataset collected using a portable device. Our proposed method achieves ROC-AUC = 0.984 / F1 = 0.940 with only 10 beats per class per subject on the test set and also achieves ROC-AUC = 0.965 / F1 = 0.937 on a real-world clinical collected data. Experimental results demonstrate that our proposed approach outperforms existing comparative methods across all evaluation metrics, and have a tendency to address intra-subject diversity. Ablation studies confirm that the combination of MAML and CL leads to more uniform performance across individuals, and our enhanced pre-fine-tuning technique substantially improves model adaptation to individual-specific data.

Identifiers

PMID41061017
PMCPMC12507228

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.