Evidence map›Paper›PMID 40703125›Full record

ArticleEuropean heart journal. Digital health2025

A deep foundation model for electrocardiogram interpretation: enabling rare disease detection through transfer learning.

Stephanie M Hu, Joshua P Barrios, Geoffrey H Tison

Abstract read
In one paragraph

Article in European heart journal. Digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. The global roadmap for cardiovascular imaging: bridging the diagnostic divide.European heart journal. Imaging methods and practice · 2026
    Review
  4. Article
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

3 authors.

Stephanie M HuDepartment of Medicine, Division of Cardiology, University of California, San Francisco, 555 Mission Bay Blvd South, San Francisco, CA 94158, USA.
Joshua P BarriosDepartment of Medicine, Division of Cardiology, University of California, San Francisco, 555 Mission Bay Blvd South, San Francisco, CA 94158, USA.
Geoffrey H TisonDepartment of Medicine, Division of Cardiology, University of California, San Francisco, 555 Mission Bay Blvd South, San Francisco, CA 94158, USA.ORCID https://orcid.org/0000-0002-0310-3326

Funding

A physiologically-focused approach to training multi-modality AI algorithms in medicineDP2HL174046 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Geoffrey H Tison · 2023 to 2026
$2.4M
Developing a platform for deep phenotyping of heart failure with preserved ejection fraction using raw, widely-available, multi-modality data and artificial intelligence algorithmsR56HL161475 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TISON, GEOFFREY H · 2022 to 2022
$721k
NHLBI NIH HHS DP2 HL174046NHLBI NIH HHS R56 HL161475
6 · The paper itself

Abstract

In healthcare, scarcity of high-quality human-adjudicated labelled data may limit the potential of deep neural networks (DNNs). Foundation models provide an efficient starting point for deep learning that can facilitate effective DNN training with fewer labelled training examples. In this study, we leveraged cardiologist-confirmed labels from a large dataset of 1.6 million electrocardiograms (ECGs) acquired as part of routine clinical care at UCSF between 1986 and 2019 to pre-train a convolutional DNN to predict 68 common ECG diagnoses. To our knowledge, this model is one of the most comprehensive ECG DNN models to date, demonstrating high performance with a median area under the receiver operating curve (AUC) of 0.978, median sensitivity of 0.937, and median specificity of 0.923. We then demonstrate the model's utility as a foundation model by additionally training (fine-tuning) the DNN to detect three novel ECG diagnoses with relatively small datasets: carcinoid syndrome, pericardial constriction, and rheumatic doming of the mitral valve. Fine-tuning training of the foundation model achieved an AUC of 0.772 (95% CI 0.723-0.816) for carcinoid syndrome, 0.883 (0.863-0.906) for pericardial constriction, and 0.826 (95% CI 0.802-0.854) for rheumatic doming, compared to 0.492 (95% CI 0.434-0.558), 0.689 (95% CI 0.656-0.720), and 0.701 (95% CI 0.657-0.745), respectively, for DNNs trained from scratch on the same small datasets. Our results demonstrate that the ECG foundation model learned a flexible representation of ECG waveforms and can improve performance of fine-tuned downstream models, particularly in data-limited settings.

Indexed as

ArrhythmiasArtificial intelligenceElectrocardiogramNeural networkPericardial diseaseTransfer learningValvular disease

Identifiers

PMID40703125
PMCPMC12282392

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Registered trials

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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.