Article ID Journal Published Year Pages File Type
8401293 Progress in Biophysics and Molecular Biology 2014 9 Pages PDF
Abstract
Patient-specific computational models have promise to improve cardiac disease diagnosis and therapy planning. Here a new method is described to simulate left-bundle branch block (LBBB) and RV-paced ventricular activation patterns in three dimensions from non-invasive, routine clinical measurements. Activation patterns were estimated in three patients using vectorcardiograms (VCG) derived from standard 12-lead electrocardiograms (ECG). Parameters of a monodomain model of biventricular electrophysiology were optimized to minimize differences between the measured and computed VCG. Electroanatomic maps of local activation times measured on the LV and RV endocardial surfaces of the same patients were used to validate the simulated activation patterns. For all patients, the optimal estimated model parameters predicted a time-averaged mean activation dipole orientation within 6.7 ± 0.6° of the derived VCG. The predicted local activation times agreed within 11.5 ± 0.8 ms of the measured electroanatomic maps, on the order of the measurement accuracy.
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