Learning cardiac activation maps from 12-lead ECG with multi-fidelity Bayesian optimization on manifolds. Issue 20 (2022)

• Record Type: Journal Article
• Authors: Pezzuto, Simone; Perdikaris, Paris; Costabal, Francisco Sahli
• Is Part Of: IFAC-PapersOnLine. Volume 55:Issue 20(2022)
• Page Start: 175
• Page End: 180
• Publication Date: 2022
• Subjects: Manifold Gaussian Process -- Bayesian optimization -- Eikonal model -- ECG Inverse Problem -- Earliest Activation Sites Identification; Automatic control -- Periodicals; 629.805
• DOI: 10.1016/j.ifacol.2022.09.091
• Languages: English
• ISSNs: 2405-8963

Abstract

Abstract: We propose a method for identifying an ectopic activation in the heart non-invasively. Ectopic activity in the heart can trigger deadly arrhythmias. The localization of the ectopic foci or earliest activation sites (EASs) is therefore a critical information for cardiologists in deciding the optimal treatment. In this work, we formulate the identification problem as a global optimization problem, by minimizing the mismatch between the ECG predicted by a cardiac model, when paced at a given EAS, and the observed ECG during the ectopic activity. Our cardiac model amounts at solving an anisotropic eikonal equation for cardiac activation and the forward bidomain model in the torso with the lead field approach for computing the ECG. We build a Gaussian process surrogate model of the loss function on the heart surface to perform Bayesian optimization. In this procedure, we iteratively evaluate the loss function following the lower confidence bound criterion, which combines exploring the surface with exploitation of the minimum region. We also extend this framework to incorporate multiple levels of fidelity of the model. We show that our procedure converges to the minimum only after 11.7 ± 10.4 iterations (20 independent runs) for the single-fidelity case and 3.5 ± 1.7 iterations for the multi-fidelity case. We envision that this tool could be applied in real time in a clinical setting to identify potentially dangerous EASs.