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Chapter 2 Implementation of a patient-specific cardiac model 57




























                     Figure 2.15. Computational performance of the LBM-EP algorithm on different
                     architectures: single processor, multicore processing on the CPU and on the
                     graphical processing unit.


                     2.2.2 Efficient modeling of the electrical conduction
                           system

                        As discussed in section 1.2.2, the electrical conduction system
                     is a complex anatomical structure, whose geometrical and func-
                     tional properties determine the pattern of ventricular excitation
                     and contraction. To properly reproduce the sequence of cardiac
                     activation, a ventricular electrophysiology model must be able to
                     accurately capture the location and thickness of the Purkinje sys-
                     tem, including patient-specific information whenever available.
                     The effect of high-speed bundles can be modeled as a localized
                     increase of the electrical conductivity of the myocardial tissue.
                     Assuming that the left and right bundle branches, as well as the
                     Purkinje fibers, are densely diffused in the subendocardium, as re-
                     ported for instance in [58], a rule can be defined to classify the
                     myocardial tissue as part of the high-speed bundles, based on
                     its distance from the endocardium. Numerical methods based on
                     Cartesian grids pose a challenge to this approach, since the raster-
                     ization process limits the spatial accuracy of all space-dependent
                     quantities to the resolution of the grid. After the rasterization, grid
                     nodes are classified as either part of the high-speed conducting
                     tissue or part of the normal tissue. Therefore, the sub-endocardial
                     layer is approximated with an error that depends on the grid res-
                     olution. This can be a significant limitation when describing the
                     Purkinje system, that extends subendocardially in a layer whose
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