Inference of ventricular activation properties from non-invasive electrocardiography

TL;DR

This paper introduces a novel computational approach combining non-invasive ECG data with advanced cardiac modelling to accurately infer individual ventricular activation properties, aiding personalized cardiac diagnosis and treatment.

Contribution

It develops an efficient Bayesian inference method integrating Eikonal simulations and torso-biventricular models for non-invasive cardiac property estimation.

Findings

Successfully infers ventricular activation properties from non-invasive data.

Higher accuracy in identifying earliest activation sites and conduction speeds.

Effective across virtual subjects with varying cardiac volumes.

Abstract

The realisation of precision cardiology requires novel techniques for the non-invasive characterisation of individual patients' cardiac function to inform therapeutic and diagnostic decision-making. The electrocardiogram (ECG) is the most widely used clinical tool for cardiac diagnosis. Its interpretation is, however, confounded by functional and anatomical variability in heart and torso. In this study, we develop new computational techniques to estimate key ventricular activation properties for individual subjects by exploiting the synergy between non-invasive electrocardiography and image-based torso-biventricular modelling and simulation. More precisely, we present an efficient sequential Monte Carlo approximate Bayesian computation-based inference method, integrated with Eikonal simulations and torso-biventricular models constructed based on clinical cardiac magnetic resonance (CMR) imaging. The method also includes a novel strategy to treat combined continuous (conduction speeds) and discrete (earliest activation sites) parameter spaces, and an efficient dynamic time warping-based ECG comparison algorithm. We demonstrate results from our inference method on a cohort of twenty virtual subjects with cardiac volumes ranging from 74 cm3 to 171 cm3 and considering low versus high resolution for the endocardial discretisation (which determines possible locations of the earliest activation sites). Results show that our method can successfully infer the ventricular activation properties from non-invasive data, with higher accuracy for earliest activation sites, endocardial speed, and sheet (transmural) speed in sinus rhythm, rather than the fibre or sheet-normal speeds.