Detecting Left Ventricular Systolic Dysfunction on Standard 12-Lead ECG Using a Smartphone-Based Deep Neural Network

  • Powerful Medical
  • March 30, 2025
  • 3 min to read
ACC.25 abstract cover — ROC curves of the two AI-ECG models detecting LVEF ≤40% and LVEF <50% on the validation dataset

Overview

This Powerful Medical-led study developed two smartphone-deployable AI-ECG models (PMcardio LVsense) that detect reduced left ventricular ejection fraction (LVEF) on a standard 12-lead ECG, using ECGs and echocardiograms recorded within 24 hours of each other at a large tertiary care center between 2011 and 2021. In an independent validation set of 25,510 ECG–echocardiogram pairs from unique patients, the LVEF <50% model reached an AUC of 0.952 and the LVEF ≤40% model an AUC of 0.963. Negative predictive values were 99.0% and 99.5%, respectively. In patients whose echocardiogram showed normal LVEF, a discordant AI-ECG reading of reduced LVEF was associated with a 6.8-fold higher risk of developing LV systolic dysfunction over a median follow-up of 7.3 years.

Key findings

  • In 25,510 independent validation ECG–echocardiogram pairs, the LVEF <50% model achieved an AUC of 0.952 (95% CI 0.947–0.956), with 89.9% sensitivity and 87.5% specificity.
  • The LVEF ≤40% model achieved an AUC of 0.963 (95% CI 0.959–0.966), with 92.4% sensitivity and 88.7% specificity.
  • Negative predictive values were 99.0% (LVEF <50%) and 99.5% (LVEF ≤40%), with positive predictive values of 38.2% and 31.8%.
  • In patients with echocardiography-confirmed normal LVEF, a discordant AI-ECG reading of LVEF <50% was associated with a 6.8-fold increased risk of incident LV systolic dysfunction (HR 6.8, 95% CI 6–7.8; median follow-up 7.3 years).

Published in: ACC.25 – presented as a poster (Journal of the American College of Cardiology, Volume 85, Issue 12, Supplement A)
Published on: 30 March 2025

Background

Point-of-care tools for rapid evaluation of left ventricular (LV) systolic function are lacking. The authors aimed to develop two artificial intelligence (AI) models that detect reduced left ventricular ejection fraction (LVEF) on the 12-lead electrocardiogram (ECG) and that can be deployed using smartphones.

Methods

All ECGs and transthoracic echocardiograms (TTEs) recorded within a 24-hour window between 2011 and 2021 were retrieved from a large tertiary care center. Two independent AI-ECG models were developed to detect LVEF <50% and LVEF ≤40%, and both models were integrated with smartphone-based ECG digitization technology. Key performance metrics included the area under the receiver operating characteristic curve (AUC), sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and F1 score.

Results

A total of 1,205,370 ECGs from 198,274 patients and 291,433 TTEs from 105,849 patients were collected. After pairing ECGs with TTEs, 109,809 ECG–TTE pairs were obtained from 56,236 patients. The independent validation dataset included 25,510 unique ECG–TTE pairs from unique patients. The LVEF <50% model achieved an AUC of 0.952 (95% CI 0.947–0.956), with sensitivity 0.899 (95% CI 0.886–0.912), specificity 0.875 (0.871–0.879), PPV 0.382 (0.368–0.395) and NPV 0.990 (0.989–0.992). The LVEF ≤40% model achieved an AUC of 0.963 (95% CI 0.959–0.966), with sensitivity 0.924 (95% CI 0.910–0.937), specificity 0.887 (0.883–0.891), PPV 0.318 (0.304–0.333) and NPV 0.995 (0.994–0.996). In individuals with echocardiography-confirmed normal LVEF (>50%), a discordant AI-ECG reading of reduced LVEF (<50%) was associated with a 6.8-fold increased risk of developing incident LV systolic dysfunction (HR 6.8, 95% CI 6–7.8; median follow-up 7.3 years).

Conclusion

Both AI models effectively detect reduced LVEF on 12-lead ECGs and are readily accessible via smartphone, providing a rapid and accessible screening tool. This approach enables widescale assessment of LV function in a non-specialist environment and facilitates early identification of patients who may benefit from echocardiographic evaluation.

Authors: A. Demolder, R. Herman, B. Vavrik, M. Martonak, V. Boza, M. Herman, T. Palus, V. Kresnakova, J. Bahyl, A. Iring, R. Hatala, J. Bartunek, M. Vanderheyden, W. Heggermont, M. Penicka

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