Quantitative Prediction of Right Ventricular Size and Function From the ECG

Author:

Duong Son Q.123ORCID,Vaid Akhil2ORCID,My Vy Thi Ha2ORCID,Butler Liam R.1ORCID,Lampert Joshua4,Pass Robert H.1,Charney Alexander W.25,Narula Jagat6ORCID,Khera Rohan78910ORCID,Sakhuja Ankit11,Greenspan Hayit12,Gelb Bruce D.135ORCID,Do Ron25ORCID,Nadkarni Girish N.213ORCID

Affiliation:

1. Division of Pediatric Cardiology, Department of Pediatrics Icahn School of Medicine at Mount Sinai New York NY

2. The Charles Bronfman Institute of Personalized Medicine, Icahn School of Medicine at Mount Sinai New York NY

3. Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai New York NY

4. Helmsley Center for Electrophysiology at The Mount Sinai Hospital New York NY

5. Department of Genetics and Genomic Sciences Icahn School of Medicine at Mount Sinai New York NY

6. Mount Sinai Heart, Icahn School of Medicine at Mount Sinai New York NY

7. Section of Cardiovascular Medicine, Department of Internal Medicine Yale School of Medicine New Haven CT

8. Section of Health Informatics, Department of Biostatistics Yale School of Public Health New Haven CT

9. Biomedical Informatics and Data Science, Yale School of Medicine New Haven CT

10. Center for Outcomes Research and Evaluation, Yale‐New Haven Hospital New Haven CT

11. Division of Cardiovascular Critical Care, Department of Cardiac and Thoracic Surgery West Virginia University Morgantown WV

12. Biomedical Engineering and Imaging Institute, Icahn School of Medicine at Mount Sinai New York NY

13. The Division of Data Driven and Digital Medicine (D3M), Department of Medicine Icahn School of Medicine at Mount Sinai New York NY

Abstract

Background Right ventricular ejection fraction (RVEF) and end‐diastolic volume (RVEDV) are not readily assessed through traditional modalities. Deep learning–enabled ECG analysis for estimation of right ventricular (RV) size or function is unexplored. Methods and Results We trained a deep learning–ECG model to predict RV dilation (RVEDV >120 mL/m 2 ), RV dysfunction (RVEF ≤40%), and numerical RVEDV and RVEF from a 12‐lead ECG paired with reference‐standard cardiac magnetic resonance imaging volumetric measurements in UK Biobank (UKBB; n=42 938). We fine‐tuned in a multicenter health system (MSH original [Mount Sinai Hospital]; n=3019) with prospective validation over 4 months (MSH validation ; n=115). We evaluated performance with area under the receiver operating characteristic curve for categorical and mean absolute error for continuous measures overall and in key subgroups. We assessed the association of RVEF prediction with transplant‐free survival with Cox proportional hazards models. The prevalence of RV dysfunction for UKBB/MSH original /MSH validation cohorts was 1.0%/18.0%/15.7%, respectively. RV dysfunction model area under the receiver operating characteristic curve for UKBB/MSH original /MSH validation cohorts was 0.86/0.81/0.77, respectively. The prevalence of RV dilation for UKBB/MSH original /MSH validation cohorts was 1.6%/10.6%/4.3%. RV dilation model area under the receiver operating characteristic curve for UKBB/MSH original /MSH validation cohorts was 0.91/0.81/0.92, respectively. MSH original mean absolute error was RVEF=7.8% and RVEDV=17.6 mL/m 2 . The performance of the RVEF model was similar in key subgroups including with and without left ventricular dysfunction. Over a median follow‐up of 2.3 years, predicted RVEF was associated with adjusted transplant‐free survival (hazard ratio, 1.40 for each 10% decrease; P =0.031). Conclusions Deep learning–ECG analysis can identify significant cardiac magnetic resonance imaging RV dysfunction and dilation with good performance. Predicted RVEF is associated with clinical outcome.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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