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A stabilized linear finite element method for anisotropic poroelastodynamics with application to cardiac perfusion
Namshad Thekkethil1, Simone Rossi2, Hao Gao1
1School of Mathematics and Statistics, University of Glasgow, Glasgow, UK.
This study introduces a new finite element method for nonlinear poroelasticity, crucial for understanding heart mechanics. The method accurately models anisotropic tissue, revealing its significant impact on pore pressure dynamics in the left ventricle.
Area of Science:
- Computational mechanics
- Biomedical engineering
- Solid mechanics
Background:
- Nonlinear poroelasticity is essential for modeling biological tissues like the heart.
- Anisotropic properties of the solid skeleton significantly influence poroelastic behavior.
- Accurate numerical methods are needed for implicit time integration of complex poroelastic formulations.
Purpose of the Study:
- To develop and verify a stabilized finite element method for nonlinear poroelasticity.
- To investigate the influence of anisotropic myocardial properties on left ventricle (LV) pore pressure dynamics.
- To correlate pore pressure variations with LV dynamics and added mass.
Main Methods:
- A variational multiscale method was employed for stabilization of a linear finite element method.
- A monolithic formulation integrating structural dynamics and Darcy flow was implemented.
- The method was verified using hyperelastic and poroelastic benchmark cases and validated on a human LV model.
Main Results:
- The numerical method demonstrated second-order accuracy in grid convergence studies.
- Simulations showed that myocardial anisotropicity substantially affects pore pressure.
- Pore pressure variations were correlated with LV dynamics, peaking at systole.
Conclusions:
- The proposed method accurately simulates nonlinear poroelasticity, particularly for anisotropic biological tissues.
- Myocardial anisotropicity plays a critical role in cardiac pore pressure regulation.
- The findings provide valuable insights into the biomechanics of the left ventricle.
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