Simulating Cardiac Fluid Dynamics in the Human Heart
Cardiac fluid dynamics fundamentally involves interactions between complex blood flows and the structural deformations of the muscular heart walls and the thin, flexible valve leaflets. There has been longstanding scientific, engineering, and medical interest in creating mathematical models of the h...
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Zusammenfassung: | Cardiac fluid dynamics fundamentally involves interactions between complex
blood flows and the structural deformations of the muscular heart walls and the
thin, flexible valve leaflets. There has been longstanding scientific,
engineering, and medical interest in creating mathematical models of the heart
that capture, explain, and predict these fluid-structure interactions. However,
existing computational models that account for interactions among the blood,
the actively contracting myocardium, and the cardiac valves are limited in
their abilities to predict valve performance, resolve fine-scale flow features,
or use realistic descriptions of tissue biomechanics. Here we introduce and
benchmark a comprehensive mathematical model of cardiac fluid dynamics in the
human heart. A unique feature of our model is that it incorporates
biomechanically detailed descriptions of all major cardiac structures that are
calibrated using tensile tests of human tissue specimens to reflect the heart's
microstructure. Further, it is the first fluid-structure interaction model of
the heart that provides anatomically and physiologically detailed
representations of all four cardiac valves. We demonstrate that this
integrative model generates physiologic dynamics, including realistic
pressure-volume loops that automatically capture isovolumetric contraction and
relaxation, and predicts fine-scale flow features. None of these outputs are
prescribed; instead, they emerge from interactions within our comprehensive
description of cardiac physiology. Such models can serve as tools for
predicting the impacts of medical devices or clinical interventions. They also
can serve as platforms for mechanistic studies of cardiac pathophysiology and
dysfunction, including congenital defects, cardiomyopathies, and heart failure,
that are difficult or impossible to perform in patients. |
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DOI: | 10.48550/arxiv.2307.02680 |