Key result
AI-ECG predicts CMR-defined LV dysfunction with an AUROC of 0.89.
Why the study?
AI-ECG analysis shows promise for detecting biventricular pathophysiology, but remains underexplored in congenital heart disease.
Does an AI-ECG model accurately predict CMR-defined biventricular dysfunction and dilation in patients with congenital heart disease?
Observational (n=5,687)
Yes
Does an AI-ECG model accurately predict CMR-defined biventricular dysfunction and dilation in patients with congenital heart disease?
Effect estimate: AUROC 0.89
An AI-ECG model can accurately predict CMR-defined biventricular dysfunction and dilation in patients with congenital heart disease, potentially serving as a cost-effective screening tool to guide CMR timing.
Background: Artificial intelligence–enhanced ECG (AI-ECG) analysis shows promise to detect biventricular pathophysiology. However, AI-ECG analysis remains underexplored in congenital heart disease (CHD). Objectives: To develop and externally validate an AI-ECG model to predict cardiovascular magnetic resonance (CMR)-defined biventricular dysfunction/dilation in patients with CHD. Methods: We trained (80%) and tested (20%) a convolutional neural network on paired ECG-CMRs (≤30 days apart) from patients with and without CHD to detect left ventricular (LV) dysfunction (ejection fraction ≤40%), RV dysfunction (ejection fraction ≤35%), and LV and RV dilation (end-diastolic volume z-score ≥4). Performance was assessed during internal testing and external validation on an outside healthcare system using area under receiver operating (AUROC) and precision recall (AUPRC) curves. Results: The internal and external cohorts comprised of 8,584 ECG-CMR pairs (4,941 patients; median CMR age 20.7 years) and 909 ECG-CMR pairs (746 patients; median CMR age 25.4 years), respectively. Model performance was similar for internal testing (AUROC: LV dysfunction 0.87; LV dilation 0.86; RV dysfunction 0.88; RV dilation 0.81) and external validation (AUROC: LV dysfunction 0.89; LV dilation 0.83; RV dysfunction 0.82; RV dilation 0.80). Model performance was lowest in functionally single ventricle patients. Tetralogy of Fallot patients predicted at high-risk of ventricular dysfunction had lower survival (p<0.001). Model explainability via saliency mapping revealed lateral precordial leads influence all outcome predictions, with high-risk features including QRS widening and T wave inversions for RV dysfunction/dilation. Conclusions: AI-ECG shows promise to predict biventricular dysfunction/dilation, which may help inform CMR timing in CHD.
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Mayourian et al. (2024) conducted an observational in Congenital heart disease (n=5,687). Artificial intelligence-enhanced ECG (AI-ECG) analysis was evaluated on Prediction of left ventricular dysfunction (ejection fraction ≤40%) (AUROC 0.89). An artificial intelligence-enhanced ECG model accurately predicted cardiovascular magnetic resonance-defined left ventricular dysfunction with an external validation AUROC of 0.89.
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