Evidence map›Paper›PMID 38405776›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Artificial Intelligence-Based Automated Interpretation of Images of Electrocardiograms: Development and Multinational Validation of ECG-GPT.

Akshay Khunte, Veer Sangha, Evangelos K Oikonomou, Lovedeep S Dhingra, Arya Aminorroaya, Andreas Coppi, Sumukh Vasisht Shankar, Elijah Rockers, Bobak J Mortazavi, Deepak L Bhatt and 5 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Akshay KhunteSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0000-0003-3812-3260
Veer SanghaSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-8524-1203
Evangelos K OikonomouSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0000-0003-4362-0720
Lovedeep S DhingraSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-5664-4126
Arya AminorroayaSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0000-0003-3197-2657
Andreas CoppiSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-5243-552X
Sumukh Vasisht ShankarSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0009-0005-3034-0641
Elijah RockersCenter for Cardiovascular Computational & Precision Health, Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA.ORCID 0000-0003-1488-7661
Bobak J MortazaviCenter for Outcomes Research and Evaluation, Yale-New Haven Hospital, New Haven, CT.ORCID 0000-0002-2655-2095
Deepak L BhattMount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai, New York, NY.ORCID 0000-0002-1278-6245
Harlan M KrumholzSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0000-0003-2046-127X
Sadeer Al-KindiCenter for Cardiovascular Computational & Precision Health, Houston Methodist DeBakey Heart & Vascular Center, Houston, TX, USA.
Girish N NadkarniThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0001-6319-4314
Akhil VaidThe Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0002-3343-744X
Rohan KheraSection of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.ORCID 0000-0001-9467-6199

Funding

Deep learning enhanced detection and personalized monitoring of aortic stenosis - The DETECT-AS StudyR01AG089981 · NIA · YALE UNIVERSITY · PI Rohan Khera · 2024 to 2026
$2.4M
Translating Personalized Inference from Randomized Clinical Trials to Real-World Cardiovascular CareR01HL167858 · NHLBI · YALE UNIVERSITY · PI Rohan Khera · 2024 to 2026
$2.3M
Evaluating and Improving Utilization of Evidence-Based Medical Therapy in Patients with Heart Failure using Automated Tools in the Electronic Health RecordK23HL153775 · NHLBI · YALE UNIVERSITY · PI KHERA, ROHAN · 2021 to 2025
$918k
A multi-modal approach for efficient, point-of-care screening of hypertrophic cardiomyopathyF32HL170592 · NHLBI · YALE UNIVERSITY · PI OIKONOMOU, EVANGELOS · 2023 to 2024
$166k
NHLBI NIH HHS F32 HL170592NHLBI NIH HHS K23 HL153775NHLBI NIH HHS R01 HL167858NIA NIH HHS R01 AG089981
6 · The paper itself

Abstract

Background: Timely and accurate assessment of electrocardiograms (ECGs) is crucial for diagnosing, triaging, and clinically managing patients. Current workflows rely on computerized ECG interpretation tools built into ECG signal acquisition systems, which use rule-based algorithms that are unreliable and frequently not available in low-resource settings. We developed and validated a format-independent vision encoder-decoder model - ECG-GPT - that can generate free-text, expert-level interpretations directly from 12-lead ECG images. Methods: Using 12-lead ECGs and their corresponding diagnosis statements collected at the Yale-New Haven Health System (YNHHS) between 2000 and 2022, we developed a vision-text transformer model to generate interpretation statements from images of ECGs. Using structured clinical assessment, semantic similarity, and conventional natural language generation metrics, we validated ECG-GPT across 7 geographically distinct health settings. These include (1) 3 large and diverse US health systems, (2) consecutive ECGs from a central reading system in Minas Gerais, Brazil, (3) the prospective cohort study, UK Biobank, (4) a Germany-based, publicly available repository, PTB-XL, and (5) a community hospital in Missouri. Results: Overall, 2.9 million ECGs were used for model development. The model performed well in clinical assessment across 26 extracted labels: for atrial fibrillation, sinus tachycardia, sinus bradycardia, premature atrial contractions, and premature ventricular contractions, AUROCs and AUPRCs ranged from 0.80-0.95 and 0.50-0.86, respectively. For left bundle branch block, right bundle branch block, first degree atrioventricular block, left anterior fascicular block, and left posterior fascicular block, AUROCs and AUPRCs ranged from 0.88-0.96 and 0.23-0.86, respectively. Across all 26 conditions, diagnostic accuracy ranged between 0.93-0.99. ECG-GPT identified the full context of the diagnosis statements with allied conditions. It had a median pairwise cosine similarity of 0.90 (IQR 0.83-0.97), significantly greater than the median baseline similarity of 0.73 (IQR 0.67-0.78, p<0.001). This separation between median pairwise and baseline similarity remained consistent across all 26 condition-specific subsets. The results were comparable across external validation sites. Conclusions: We developed and extensively validated a vision encoder-decoder model that generates expert-level interpretations from ECG images. This represents a scalable and accessible strategy for automated ECG analysis, especially in low-resource settings.

Identifiers

PMID38405776
PMCPMC10889032

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LicenceCC BY-NC
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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.