Evidence map›Paper›PMID 40210840›Full record

ArticleInternational journal for numerical methods in biomedical engineering2025

A Neural Network Finite Element Trileaflet Heart Valve Model Incorporating Multi-Body Contact.

Kenneth Meyer, Christian Goodbrake, Michael S Sacks

Abstract read
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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Kenneth MeyerJames T. Willerson Center for Cardiovascular Modeling and Simulation, Oden Institute for Computational Engineering and Sciences, Department of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0009-0003-1087-0317
Christian GoodbrakeJames T. Willerson Center for Cardiovascular Modeling and Simulation, Oden Institute for Computational Engineering and Sciences, Department of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0003-1560-3042
Michael S SacksJames T. Willerson Center for Cardiovascular Modeling and Simulation, Oden Institute for Computational Engineering and Sciences, Department of Biomedical Engineering, The University of Texas at Austin, Austin, Texas, USA.ORCID https://orcid.org/0000-0003-0198-9212

Funding

Quantitative Methods for Optimizing IMR RepairR01HL073021 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI GORMAN, ROBERT C, SACKS, MICHAEL S · 2004 to 2022
$7.6M
Biomechanical indicators of bicuspid aortic valve dysfunctionR01HL142504 · NHLBI · UNIVERSITY OF TEXAS AT AUSTIN · PI GORMAN, ROBERT C, HSU, MING-CHEN · 2018 to 2021
$2.9M
Novel Simulation Technologies for BHV Long-Term DurabilityR01HL129077 · NHLBI · UNIVERSITY OF TEXAS AT AUSTIN · PI HUGHES, THOMAS J., MANNING, KEEFE B · 2016 to 2019
$2.1M
NHLBI NIH HHS R01 HL073021NHLBI NIH HHS R01 HL129077NHLBI NIH HHS R01 HL142504NIH HHS HL073021NIH HHS HL142504
6 · The paper itself

Abstract

The use of patient-specific computational modeling of cardiovascular diseases has become increasingly popular to improve patient standard of care. Most simulation approaches currently utilize the finite element method (FEM), which is very well established and succeeds in producing high-fidelity results. However, it remains too slow for use in clinical settings, especially when many-query solutions are required to determine optimal therapeutic approaches. As a step toward addressing these demands, we have developed a Neural Network Finite Element (NNFE) approach that greatly accelerates simulations of soft tissue organ function. While the NNFE method utilizes conventional FEM meshes to define the problem geometry, it leverages advancements in neural network architecture design in new GPU-based software tools to solve the governing hyperelastic material PDEs. The NNFE method has recently captured physical contact between a deformable body and a frictionless symmetry plane. In the present work, we extended the NNFE approach to simulate trileaflet heart valve closure as a critical step in moving toward patient-specific applications. Our approach addressed two critical aspects of heart valve simulations: the use of 3D solid leaflet models as opposed to shell-based leaflet models and multi-body contact between the leaflets. We verified the approach by comparing displacements of NNFE simulated closure of a single heart valve leaflet against a frictionless symmetry plane with an identical simulation in tIGAr, the open-source isogeometric analysis extension of FEniCS. The average nodal displacement error was 0.020 mm (0.47% of the maximum displacement). We further evaluated our implementation by varying leaflet collagen fiber directions to mimic physiologically accurate deformation modes. Results of the approach indicated that the observed leaflet deformation patterns agreed well with previous trileaflet simulations. Significant variations in stress were observed transmurally, underscoring the need for solid elements to model leaflet geometry. Computational speed improvements produced an approximately 100-fold speedup, with the NNFE simulations of single leaflet closure taking 0.28 s while its FE counterpart took 61 s. Full trileaflet valve models with multi-body contact simulations took approximately 5 s, whereas equivalent FEM simulations take several hours. Training the full trileaflet model took approximately 16 h and was trained over the full functional range of pressure, so that training was only required once for all subsequent simulations. We conclude that the NNFE method can be successfully used to perform rapid simulations of complex 3D soft organ systems, such as the trileaflet heart valve, that involve large deformations, 3D geometries, and multi-body contact. Moreover, the ability to perform post-trained simulations in dramatically shorter time periods underscores the promise of machine learning-based computational mechanics approaches in patient-specific predictive computational models.

Indexed as

Finite Element AnalysisHeart ValvesModels, CardiovascularNeural Networks, ComputerComputer SimulationHumans3D modelingcontactheart valveneural networkssimulations

Identifiers

PMID40210840
PMCPMC12044607

What OpenQuestion holds

Textmetadata
LicenceTDM
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.