A computational modeling pipeline demonstrated that a mitral valve model with a feature size of about 5 mm and mesh size of about 1 mm was sufficient to predict overall shape, stress, and strain.
Does a multi-resolution computational modeling pipeline accurately predict mitral valve biomechanics?
A novel computational pipeline enables accurate biomechanical simulations of the mitral valve in normal, dilated, and repaired states using a 5 mm feature size and 1 mm mesh size.
Multiple studies have demonstrated that the pathological geometries unique to each patient can affect the durability of mitral valve (MV) repairs. While computational modeling of the MV is a promising approach to improve the surgical outcomes, the complex MV geometry precludes use of simplified models. Moreover, the lack of complete in vivo geometric information presents significant challenges in the development of patient-specific computational models. There is thus a need to determine the level of detail necessary for predictive MV models. To address this issue, we have developed a novel pipeline for building attribute-rich computational models of MV with varying fidelity directly from the in vitro imaging data. The approach combines high-resolution geometric information from loaded and unloaded states to achieve a high level of anatomic detail, followed by mapping and parametric embedding of tissue attributes to build a high-resolution, attribute-rich computational models. Subsequent lower resolution models were then developed and evaluated by comparing the displacements and surface strains to those extracted from the imaging data. We then identified the critical levels of fidelity for building predictive MV models in the dilated and repaired states. We demonstrated that a model with a feature size of about 5 mm and mesh size of about 1 mm was sufficient to predict the overall MV shape, stress, and strain distributions with high accuracy. However, we also noted that more detailed models were found to be needed to simulate microstructural events. We conclude that the developed pipeline enables sufficiently complex models for biomechanical simulations of MV in normal, dilated, repaired states.
Drach et al. (Fri,) conducted a other in Mitral valve pathology. Multi-resolution computational modeling pipeline was evaluated on Model predictive capability for displacements and surface strains. A computational modeling pipeline demonstrated that a mitral valve model with a feature size of about 5 mm and mesh size of about 1 mm was sufficient to predict overall shape, stress, and strain.
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