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1.
Biomech Model Mechanobiol ; 18(5): 1415-1427, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31025130

ABSTRACT

Computational models of the heart have reached a level of maturity that enables sophisticated patient-specific simulations and hold potential for important applications in diagnosis and therapy planning. However, such clinical use puts strict demands on the reliability and accuracy of the models and requires the sensitivity of the model predictions due to errors and uncertainty in the model inputs to be quantified. The models typically contain a large number of parameters, which are difficult to measure and therefore associated with considerable uncertainty. Additionally, patient-specific geometries are usually constructed by semi-manual processing of medical images and must be assumed to be a potential source of model uncertainty. In this paper, we assess the model accuracy by considering the impact of geometrical uncertainties, which typically occur in image-based computational geometries. An approach based on 17 AHA segments diagram is used to consider uncertainties in wall thickness and also in the material properties and fiber orientation, and we perform a comprehensive uncertainty quantification and sensitivity analysis based on polynomial chaos expansions. The quantities considered include stress, strain and global deformation parameters of the left ventricle. The results indicate that important quantities of interest may be more affected by wall thickness, and highlight the need for accurate geometry reconstructions in patient-specific cardiac mechanics models.


Subject(s)
Heart Ventricles/anatomy & histology , Models, Cardiovascular , Uncertainty , Ventricular Function/physiology , Biomechanical Phenomena , Calibration , Humans , Stress, Mechanical
2.
Int J Numer Method Biomed Eng ; 34(4): e2948, 2018 04.
Article in English | MEDLINE | ID: mdl-29181888

ABSTRACT

Computational modeling of the heart is a subject of substantial medical and scientific interest, which may contribute to increase the understanding of several phenomena associated with cardiac physiological and pathological states. Modeling the mechanics of the heart have led to considerable insights, but it still represents a complex and a demanding computational problem, especially in a strongly coupled electromechanical setting. Passive cardiac tissue is commonly modeled as hyperelastic and is characterized by quasi-incompressible, orthotropic, and nonlinear material behavior. These factors are known to be very challenging for the numerical solution of the model. The near-incompressibility is known to cause numerical issues such as the well-known locking phenomenon and ill-conditioning of the stiffness matrix. In this work, the augmented Lagrangian method is used to handle the nearly incompressible condition. This approach can potentially improve computational performance by reducing the condition number of the stiffness matrix and thereby improving the convergence of iterative solvers. We also improve the performance of iterative solvers by the use of an algebraic multigrid preconditioner. Numerical results of the augmented Lagrangian method combined with a preconditioned iterative solver for a cardiac mechanics benchmark suite are presented to show its improved performance.


Subject(s)
Algorithms , Heart/physiology , Computer Simulation , Humans , Numerical Analysis, Computer-Assisted
4.
Article in English | MEDLINE | ID: mdl-21097059

ABSTRACT

In this work we present a new electromechanical cardiac myocyte model tailored to reproduce the electrical and force generating activities of human ventricular myocytes. The model was created by coupling two existing models: the ten Tusscher electrophysiology model and the Rice myofilament mechanics model. The parameters of the new model were adjusted in order to replicate the available experimental data for human myocytes. The main challenges in this work were the strong feedbacks between the models, the high non-linearity of the models and mainly the lack of human data to make the adjustments.


Subject(s)
Computer Simulation , Heart Ventricles/cytology , Calcium/metabolism , Heart Ventricles/metabolism , Humans , Reproducibility of Results
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