Evidence map›Paper›PMID 41441915›Full record

ArticleBiomechanics and modeling in mechanobiology2025

A multi-compartment homogenized perfusion model for deforming hierarchical vasculature.

Jannes Hohl, Adnan Ebrahem, Etienne Jessen, Marco F P Ten Eikelder, Dominik Schillinger

Abstract read
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Article in Biomechanics and modeling in mechanobiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jannes HohlInstitute for Mechanics, Computational Mechanics Group, Technical University of Darmstadt, Darmstadt, 64287, Germany. jannes.hohl@tu-darmstadt.de.ORCID http://orcid.org/0009-0002-1016-2698
Adnan EbrahemInstitute for Mechanics, Computational Mechanics Group, Technical University of Darmstadt, Darmstadt, 64287, Germany.ORCID http://orcid.org/0000-0002-8762-6158
Etienne JessenInstitute for Mechanics, Computational Mechanics Group, Technical University of Darmstadt, Darmstadt, 64287, Germany.ORCID http://orcid.org/0000-0003-0276-6029
Marco F P Ten EikelderInstitute for Mechanics, Computational Mechanics Group, Technical University of Darmstadt, Darmstadt, 64287, Germany.ORCID http://orcid.org/0000-0002-1153-146X
Dominik SchillingerInstitute for Mechanics, Computational Mechanics Group, Technical University of Darmstadt, Darmstadt, 64287, Germany.ORCID http://orcid.org/0000-0002-9068-6311

Funding

H2020 European Research Council 759001
6 · The paper itself

Abstract

The simulation of tissue perfusion based on highly detailed synthetic vasculature that often consists of multiple supplying and draining trees with millions of vascular segments is computationally expensive. Converting highly detailed synthetic vasculature into a homogenized continuum flow representation offers a computationally efficient alternative. In this paper, we investigate such a modeling approach that retains the essential features of potentially deforming hierarchical vascular networks. It is based on multi-compartment homogenization, where each compartment represents homogenized perfusion via a Darcy-type flow model associated with vascular segments at a specific spatial resolution in one individual tree of the network. The compartments are coupled through a pressure-dependent mass exchange, applied in a smeared manner everywhere within the perfusion domain. Key parameters, namely the permeability tensors of each compartment and the intercompartmental perfusion coefficients, are estimated directly from the vascular segments of the synthetic vasculature using averaging techniques. Our approach leverages spectral decomposition and a reduced set of representative vessel segments to balance computational efficiency with physical fidelity. For scenarios involving deformation, such as in a pumping heart or a regenerating liver, we introduce a computationally efficient parameter update based on geometric mapping, avoiding full re-homogenization in nonlinear simulations. We demonstrate the effectiveness and accuracy of the approach for several benchmark examples, including a full-scale multi-compartment liver perfusion simulation that explicitly incorporates three non-intersecting vascular trees, reflecting the hepatic artery, portal vein, and hepatic vein.

Indexed as

Blood VesselsModels, BiologicalModels, CardiovascularPerfusionComputer SimulationHumansLiverDarcy-type flowHierarchical vasculatureLiver perfusionMulti-compartment homogenizationSynthetic tree generationTissue perfusion

Identifiers

PMID41441915
PMCPMC12738679

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.