Evidence map›Paper›PMID 35649898›Full record

ArticleThe Journal of the Acoustical Society of America2022

Numerical simulation of wave propagation through interfaces using the extended finite element method for magnetic resonance elastography.

Quanshangze Du, Aline Bel-Brunon, Simon Auguste Lambert, Nahiène Hamila

Abstract read
In one paragraph

Article in The Journal of the Acoustical Society of America, 2022. 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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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Quanshangze DuUniv Lyon, INSA Lyon, CNRS, LaMCoS, UMR5259, 69621 Villeurbanne, France.
Aline Bel-BrunonUniv Lyon, INSA Lyon, CNRS, LaMCoS, UMR5259, 69621 Villeurbanne, France.ORCID 0000-0002-2398-9064
Simon Auguste LambertUniversité de Lyon, INSA Lyon, Université Claude Bernard Lyon 1, Ecole Centrale de Lyon, CNRS, Ampère UMR5005, Villeurbanne, France.
Nahiène HamilaENI Brest, UMR CNRS 6027, IRDL, F-29200 Brest, France.

Funding

Fast Numerical Modeling Of Medical Ultrasound For Therapy And ImagingR01EB012079 · NIBIB · MICHIGAN STATE UNIVERSITY · PI MCGOUGH, ROBERT J · 2010 to 2022
$2.3M
New fractional calculus models of attenuation for shear wave elasticity imagingR21EB023051 · NIBIB · MICHIGAN STATE UNIVERSITY · PI MCGOUGH, ROBERT J · 2017 to 2018
$353k
NIBIB NIH HHS R01 EB012079NIBIB NIH HHS R21 EB023051
6 · The paper itself

Abstract

Magnetic resonance elastography (MRE) is an elasticity imaging technique for quantitatively assessing the stiffness of human tissues. In MRE, finite element method (FEM) is widely used for modeling wave propagation and stiffness reconstruction. However, in front of inclusions with complex interfaces, FEM can become burdensome in terms of the model partition and computationally expensive. In this work, we implement a formulation of FEM, known as the eXtended finite element method (XFEM), which is a method used for modeling discontinuity like crack and heterogeneity. Using a level-set method, it makes the interface independent of the mesh, thus relieving the meshing efforts. We investigate this method in two studies: wave propagation across an oblique linear interface and stiffness reconstruction of a random-shape inclusion. In the first study, numerical results by XFEM and FEM models revealing the wave conversion rules at linear interface are presented and successfully compared to the theoretical predictions. The second study, investigated in a pseudo-practical application, demonstrates further the applicability of XFEM in MRE and the convenience, accuracy, and speed of XFEM with respect to FEM. XFEM can be regarded as a promising alternative to FEM for inclusion modeling in MRE.

Indexed as

Elasticity Imaging TechniquesComputer SimulationFinite Element AnalysisHumans

Identifiers

PMID35649898
PMCPMC9381142

What OpenQuestion holds

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Registered trials

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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.