ArticleJournal of mathematical biology2018
Modeling of the contrast-enhanced perfusion test in liver based on the multi-compartment flow in porous media.
Article in Journal of mathematical biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- A multi-compartment homogenized perfusion model for deforming hierarchical vasculature.Biomechanics and modeling in mechanobiology · 2025Article
- Modeling a 3-D multiscale blood-flow and heat-transfer framework for realistic vascular systems.Scientific reports · 2022Article
- Rigorous mathematical optimization of synthetic hepatic vascular trees.Journal of the Royal Society, Interface · 2022Article
- A nonlinear multi-scale model for blood circulation in a realistic vascular system.Royal Society open science · 2021Article
- Modelling the impact of clot fragmentation on the microcirculation after thrombectomy.PLoS computational biology · 2021Article
- Geometrical model of lobular structure and its importance for the liver perfusion analysis.PloS one · 2021Article
- Poster Viewing Sessions PB01-B01 to PB03-V09.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2019Article
- A new framework for assessing subject-specific whole brain circulation and perfusion using MRI-based measurements and a multi-scale continuous flow model.PLoS computational biology · 2019Article
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Authors and funding
3 authors.
Funding
Abstract
The paper deals with modeling the liver perfusion intended to improve quantitative analysis of the tissue scans provided by the contrast-enhanced computed tomography (CT). For this purpose, we developed a model of dynamic transport of the contrast fluid through the hierarchies of the perfusion trees. Conceptually, computed time-space distributions of the so-called tissue density can be compared with the measured data obtained from CT; such a modeling feedback can be used for model parameter identification. The blood flow is characterized at several scales for which different models are used. Flows in upper hierarchies represented by larger branching vessels are described using simple 1D models based on the Bernoulli equation extended by correction terms to respect the local pressure losses. To describe flows in smaller vessels and in the tissue parenchyma, we propose a 3D continuum model of porous medium defined in terms of hierarchically matched compartments characterized by hydraulic permeabilities. The 1D models corresponding to the portal and hepatic veins are coupled with the 3D model through point sources, or sinks. The contrast fluid saturation is governed by transport equations adapted for the 1D and 3D flow models. The complex perfusion model has been implemented using the finite element and finite volume methods. We report numerical examples computed for anatomically relevant geometries of the liver organ and of the principal vascular trees. The simulated tissue density corresponding to the CT examination output reflects a pathology modeled as a localized permeability deficiency.
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