Abstract
Objective: Ablation treatment of ventricular arrhythmias can be facilitated by pre-procedure planning aided by electrocardiographic inverse solution, which can help to localize the origin of arrhythmia. Our aim was to improve localization accuracy of the inverse solution by using a novel Bayesian approach. Methods: The inverse problem of electrocardiography was solved by reconstructing epicardial potentials from 120 body-surface electrocardiograms and from patient-specific geometry of the heart and torso for four patients suffering from scar-related ventricular tachycardia who underwent epicardial catheter mapping, which included pace-mapping. Simulations using dipole sources in patient-specific geometry were also performed. The proposed method, using dynamic spatio-temporal a priori constraints of the solution, was compared with classical Tikhonov methods based on fixed constraints. Results: The mean localization error of the proposed method for all available pacing sites (n=78) was significantly smaller than that achieved by Tikhonov methods; specifically, the localization accuracy for pacing in the normal tissue (n=17) was \text{8} \pm \text{6} mm (mean \pm SD) versus \text{13} \pm \text{9} mm (P < 0.00001) reported in the previous study using the same clinical data and Tikhonov regularization. Simulation experiments further supported these clinical findings. Conclusion: The promising results of in vivo and in silico experiments presented in this study provide a strong incentive to pursuing further investigation of data-driven Bayesian methods in solving the electrocardiographic inverse problem. Significance: The proposed approach to localizing origin of ventricular activation sequence may have important applications in pre-procedure assessment of arrhythmias and in guiding their ablation treatment.
Original language | English |
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Article number | 8477091 |
Pages (from-to) | 1380-1389 |
Number of pages | 10 |
Journal | IEEE Transactions on Biomedical Engineering |
Volume | 66 |
Issue number | 5 |
DOIs | |
Publication status | Published - May 2019 |
Bibliographical note
Funding Information:This work was supported in part by the Natural Sciences and Engineering Research Council of Canada, in part by the Canadian Institutes of Health Research, in part by the Nova Scotia Health Research Foundation, and in part by the Nova Scotia Research and Innovation Graduate Scholarship. The work of S. Zhou was supported by the Heart and Stroke Foundation of Nova Scotia.
Publisher Copyright:
© 1964-2012 IEEE.
ASJC Scopus Subject Areas
- Biomedical Engineering