Jun-Ichi Okada 1 , Teruyoshi Sasaki , Takumi Washio , Hiroshi Yamashita , Taro Kariya , Yasushi Imai , Machiko Nakagawa , Yoshimasa Kadooka , Ryozo Nagai , Toshiaki Hisada , Seiryo Sugiura . Show Affiliations »
Abstract
BACKGROUND: Recent studies, supported by advances in computer science, have successfully simulated the excitation and repolarization processes of the heart, based on detailed cell models of electrophysiology and implemented with realistic morphology. METHODS: In this study, we extend these approaches to simulate the body surface electrocardiogram (ECG) of specific individuals. Patient-specific finite element models of the heart and torso are created for four patients with various heart diseases, based on clinical data including computer tomography, while the parallel multi-grid method is used to solve the dynamic bi-domain problem. Personalization procedures include demarcation of nonexcitable tissue, allocation of the failing myocyte model of electrophysiology, and modification of the excitation sequence. In particular, the adjustment of QRS morphology requires iterative computations, facilitated by the simultaneous visualization of the propagation of excitation in the heart, average QRS vector in the torso, and 12-lead ECG. RESULTS: In all four cases we obtained reasonable agreement between the simulated and actual ECGs. Furthermore, we also simulated the ECGs of three of the patients under bi-ventricular pacing, and once again successfully reproduced the actual ECG morphologies. Since no further adjustments were made to the heart models in the pacing simulations, the good agreement provides strong support for the validity of the models. CONCLUSIONS: These results not only help us understand the cellular basis of the body surface ECG, but also open the possibility of heart simulation for clinical applications. ©2013, The Authors. Journal compilation ©2013 Wiley Periodicals, Inc.
BACKGROUND: Recent studies, supported by advances in computer science, have successfully simulated the excitation and repolarization processes of the heart, based on detailed cell models of electrophysiology and implemented with realistic morphology. METHODS: In this study, we extend these approaches to simulate the body surface electrocardiogram (ECG) of specific individuals. Patient -specific finite element models of the heart and torso are created for four patients with various heart diseases , based on clinical data including computer tomography, while the parallel multi-grid method is used to solve the dynamic bi-domain problem. Personalization procedures include demarcation of nonexcitable tissue, allocation of the failing myocyte model of electrophysiology, and modification of the excitation sequence. In particular, the adjustment of QRS morphology requires iterative computations, facilitated by the simultaneous visualization of the propagation of excitation in the heart, average QRS vector in the torso, and 12-lead ECG. RESULTS: In all four cases we obtained reasonable agreement between the simulated and actual ECGs. Furthermore, we also simulated the ECGs of three of the patients under bi-ventricular pacing, and once again successfully reproduced the actual ECG morphologies. Since no further adjustments were made to the heart models in the pacing simulations, the good agreement provides strong support for the validity of the models. CONCLUSIONS: These results not only help us understand the cellular basis of the body surface ECG, but also open the possibility of heart simulation for clinical applications. ©2013, The Authors. Journal compilation ©2013 Wiley Periodicals, Inc.
Entities: Disease
Species
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Year: 2013
PMID: 23461560 DOI: 10.1111/pace.12057
Source DB: PubMed Journal: Pacing Clin Electrophysiol ISSN: 0147-8389 Impact factor: 1.976