Noninvasive Personalization of a Cardiac Electrophysiology Model From Body Surface Potential Mapping.

GOAL: We use noninvasive data (body surface potential mapping, BSPM) to personalize the main parameters of a cardiac electrophysiological (EP) model for predicting the response to different pacing conditions.

METHODS: First, an efficient forward model is proposed, coupling the Mitchell-Schaeffer transmembrane potential model with a current dipole formulation. Then, we estimate the main parameters of the cardiac model: activation onset location and tissue conductivity. A large patient-specific database of simulated BSPM is generated, from which specific features are extracted to train a machine learning algorithm. The activation onset location is computed from a Kernel Ridge Regression and a second regression calibrates the global ventricular conductivity.

RESULTS: The evaluation of the results is done both on a benchmark dataset of a patient with premature ventricular contraction (PVC) and on five nonischaemic implanted cardiac resynchonization therapy (CRT) patients with a total of 21 different pacing conditions. Good personalization results were found in terms of the activation onset location for the PVC (mean distance error, MDE = 20.3 mm), for the pacing sites (MDE = 21.7 mm) and for the CRT patients (MDE = 24.6 mm). We tested the predictive power of the personalized model for biventricular pacing and showed that we could predict the new electrical activity patterns with a good accuracy in terms of BSPM signals.

CONCLUSION: We have personalized the cardiac EP model and predicted new patient-specific pacing conditions.

SIGNIFICANCE: This is an encouraging first step towards a noninvasive preoperative prediction of the response to different pacing conditions to assist clinicians for CRT patient selection and therapy planning.