TY - JOUR
T1 - Dimensional reduction of a poromechanical cardiac model for myocardial perfusion studies
AU - Chabiniok, Radomír
AU - Burtschell, Bruno
AU - Chapelle, Dominique
AU - Moireau, Philippe
N1 - Funding Information:
We are grateful to Dr. Fabrice Vallée, Anesthesiology and Intensive Care Department, Lariboisière - Saint Louis - Fernand Widal University Hospitals, Paris, France, for several valuable discussions.
Publisher Copyright:
© 2022 The Authors
PY - 2022/12
Y1 - 2022/12
N2 - In this paper, we adapt a previously developed poromechanical formulation to model the perfusion of myocardium during a cardiac cycle. First, a complete model is derived in 3D. Then, we perform a dimensional reduction under the assumption of spherical symmetry and propose a numerical algorithm that enables us to perform simulations of the myocardial perfusion throughout the cardiac cycle. These simulations illustrate the use of the proposed model to represent various physiological and pathological scenarios, specifically the vasodilation in the coronary network (to reproduce the standard clinical assessment of myocardial perfusion and perfusion reserve), the stenosis of a large coronary artery, an increased vascular resistance in the microcirculation (microvascular disease) and the consequences of inotropic activation (increased myocardial contractility) particularly at the level of the systolic flow impediment. Our results show that the model gives promising qualitative reproductions of complex physiological phenomena. This paves the way for future quantitative studies using clinical or experimental data.
AB - In this paper, we adapt a previously developed poromechanical formulation to model the perfusion of myocardium during a cardiac cycle. First, a complete model is derived in 3D. Then, we perform a dimensional reduction under the assumption of spherical symmetry and propose a numerical algorithm that enables us to perform simulations of the myocardial perfusion throughout the cardiac cycle. These simulations illustrate the use of the proposed model to represent various physiological and pathological scenarios, specifically the vasodilation in the coronary network (to reproduce the standard clinical assessment of myocardial perfusion and perfusion reserve), the stenosis of a large coronary artery, an increased vascular resistance in the microcirculation (microvascular disease) and the consequences of inotropic activation (increased myocardial contractility) particularly at the level of the systolic flow impediment. Our results show that the model gives promising qualitative reproductions of complex physiological phenomena. This paves the way for future quantitative studies using clinical or experimental data.
KW - Biomechanical modeling
KW - Computational physiology
KW - Ischemic heart disease
KW - Microvascular disease
KW - Myocardial perfusion
KW - Poroelasticity
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U2 - 10.1016/j.apples.2022.100121
DO - 10.1016/j.apples.2022.100121
M3 - Article
AN - SCOPUS:85142820409
SN - 2666-4968
VL - 12
JO - Applications in Engineering Science
JF - Applications in Engineering Science
M1 - 100121
ER -