Evidence map›Paper›PMID 41369131›Full record

ArticleInternational journal for numerical methods in biomedical engineering2025

A Comparison of Coupling Strategies for 1D-3D Simulations of Coronary Hemodynamics.

P L J Hilhorst, A J E Vermeer, K Zając, M van 't Veer, M Rezaeimoghaddam, F N van de Vosse, W Huberts

Abstract readComparative Study
In one paragraph

Article in International journal for numerical methods in biomedical engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. A Comparison of Coupling Strategies for 1D-3D Simulations of Coronary Hemodynamics.International journal for numerical methods in biomedical engineering · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

P L J HilhorstDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0003-1764-1536
A J E VermeerDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0009-0008-8149-2110
K ZającSano Centre for Computational Medicine, Kraków, Poland.ORCID https://orcid.org/0000-0003-1393-8236
M van 't VeerDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-5006-0111
M RezaeimoghaddamDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-0539-1616
F N van de VosseDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-4084-2064
W HubertsDepartment of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, the Netherlands.ORCID https://orcid.org/0000-0002-0779-4785

Funding

European Union's Horizon 2020 Research and Innovation Programme Through the Research and Innovation Actions "In Silico World: Lowering Barriers to Ubiquitous Adoption of In Silico Trials" 101016503Polish High-Performance Computing Infrastructure PLGrid (HPC Center: ACK Cyfronet AGH) PLG/2024/017022Polish High-Performance Computing Infrastructure PLGrid (HPC Center: ACK Cyfronet AGH) PLG/2024/017108
6 · The paper itself

Abstract

Noninvasive prediction of Fractional Flow Reserve (FFR) from imaging data through computational modeling has emerged as a promising alternative to invasive pressure measurements. Simulating coronary physiology, specifically coronary stenosis, poses a significant challenge due to the complex geometries of stenotic lesions and the need for physiologically realistic boundary conditions. Coupled 1D-3D modeling frameworks integrate a global one-dimensional (1D) circulation model with localized three-dimensional (3D) Computational Fluid Dynamics (CFD), enabling dynamic updates of boundary conditions and more accurate hemodynamic simulation. In this study, we couple a global 1D model of the coronary tree and partial systemic circulation with 3D CFD simulations using synthetically generated coronary stenosis geometries. We created three lesion types-symmetric, eccentric, and irregular-at severities of 50%, 70%, and 80%, to evaluate explicit coupling strategies for FFR prediction. We compare a steady-state 3D simulation driven by mean flow from the transient 1D model with transient 3D simulations that exchange data continuously at every step or only at the end of the converged cardiac cycle. Applied to the synthetic stenotic geometries, all approaches predicted similar FFR values, while the steady-state strategy achieved a significant reduction in computational cost, rendering it the most efficient for FFR prediction. Moreover, for irregular lesion geometries, localized 3D modeling revealed discrepancies in pressure loss compared to a simplified lumped model, demonstrating the added value of high-fidelity 3D simulations in complex cases.

Indexed as

Coronary CirculationCoronary VesselsHemodynamicsModels, CardiovascularComputer SimulationCoronary StenosisFractional Flow Reserve, MyocardialHumansHydrodynamicsImaging, Three-Dimensionalcomputational fluid dynamicscoronary hemodynamicspatient‐specific modelingpulse‐wave propagation modelreduced‐order modeling

Identifiers

PMID41369131
PMCPMC12691134

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.