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Updated: Sep 10, 2026

Signal Acquisition, Score Interpretation, and Economics of a Non-Invasive Point-of-Care Test for Coronary Artery Disease
Published on: August 9, 2024
Electro-mechanical risk score for coronary artery disease risk estimation using seismocardiography
Parastoo Dehkordi1, Kouhyar Tavakolian2, Thomas Rocco3
1Research and Development Department, HeartForce Medical Inc., 1201-570 Granville Street, Vancouver, BC V6C 1W6, Canada.
Aims:
Coronary artery disease (CAD) remains a leading cause of morbidity. Existing clinical likelihood models often lack specificity, contributing to unnecessary diagnostic testing. To develop, train, and validate the electro-mechanical risk (EMR) Score. This machine learning model uses cardiac mechanical information from resting seismocardiography (SCG) recordings and patient-level clinical risk factors to estimate obstructive CAD likelihood.
Methods And Results:
This multi-centre clinical study included 2110 adults. Resting SCG was recorded using a sternum accelerometer. Obstructive CAD was defined as 50% or greater stenosis on coronary computed tomography angiography or invasive coronary angiography. A one-dimensional convolutional neural network was trained to compute the EMR Score. Performance was evaluated using repeated cross-validation and external-centre validation and compared with the 2024 ESC Risk-Factor-weighted Clinical Likelihood (RF-CL) model. Among 2110 participants (mean [SD] age, 57.8 [10.3] years; 801 women [38%]), 760 had obstructive CAD. In symptomatic individuals, the EMR Score achieved an AUC of 0.88, outperforming RF-CL (AUC, 0.85; P = 0.023), with higher specificity (53% vs. 35%) and comparable sensitivity (94% vs. 97%). In external-centre validation, the EMR Score achieved an AUC of 0.91, sensitivity of 97.8%, specificity of 52.0%, PPV of 78.0%, and NPV of 93.0%. In asymptomatic participants, the AUC was 0.89. The EMR Score classified 23% of the cohort as very low likelihood, with 2% CAD prevalence.
Conclusion:
The EMR Score non-invasively estimated obstructive CAD likelihood, with external-centre validation supporting generalizability beyond internal cross-validation.
Clinical Trial Registration:
ClinicalTrials.gov (NCT06880120, NCT06880133).
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