Evidence map›Paper›PMID 19727874›Full record

ArticleBiomechanics and modeling in mechanobiology2010

Adaptive generation of multimaterial grids from imaging data for biomedical Lagrangian fluid-structure simulations.

James P Carson, Andrew P Kuprat, Xiangmin Jiao, Volodymyr Dyedov, Facundo Del Pin, Julius M Guccione, Mark B Ratcliffe, Daniel R Einstein

Abstract read
In one paragraph

Article in Biomechanics and modeling in mechanobiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. A chicken embryo cardiac outflow tract atlas for registering changes due to abnormal blood flow.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference · 2016
    Article
  5. Article
  6. Article
  7. Comparative computational modeling of airflows and vapor dosimetry in the respiratory tracts of rat, monkey, and human.Toxicological sciences : an official journal of the Society of Toxicology · 2012
    Article
  8. Article
  9. 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

8 authors.

James P CarsonBiological Monitoring and Modeling, Pacific Northwest National Laboratory, Richland, WA, USA. james.carson@pnl.gov
Andrew P Kuprat
Xiangmin Jiao
Volodymyr Dyedov
Facundo Del Pin
Julius M Guccione
Mark B Ratcliffe
Daniel R Einstein

Funding

3D IMAGING &COMPUTER MODEL OF THE RESPIRATORY TRACTR01HL073598 · NHLBI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI CORLEY, RICHARD A · 2004 to 2014
$17.6M
VIRTUAL TOOLS FOR CARDIAC VENTRICULAR REMODELING SURGERYR01HL077921 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GUCCIONE, JULIUS MATTEO · 2006 to 2015
$3.4M
Surgery for Ischemic Mitral RegurgitationR01HL084431 · NHLBI · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI RATCLIFFE, MARK B · 2008 to 2011
$2.5M
NCI NIH HHS P41 RR05959/U24 CA092656NHLBI NIH HHS 1R01HL073598-01A1NHLBI NIH HHS 1R01HL084431-01A1NHLBI NIH HHS R01 HL073598NHLBI NIH HHS R01 HL077921NHLBI NIH HHS R01 HL084431
6 · The paper itself

Abstract

Spatial discretization of complex imaging- derived fluid-solid geometries, such as the cardiac environment, is a critical but often overlooked challenge in biomechanical computations. This is particularly true in problems with Lagrangian interfaces, where the fluid and solid phases share a common interface geometrically. For simplicity and better accuracy, it is also highly desirable for the two phases to have a matching surface mesh at the interface between them. We outline a method for solving this problem, and illustrate the approach with a 3D fluid-solid mesh of the mouse heart. An MRI dataset of a perfusion-fixed mouse heart with 50 microm isotropic resolution was semi-automatically segmented using a customized multimaterial connected-threshold approach that divided the volume into non-overlapping regions of blood, tissue, and background. Subsequently a multimaterial marching cubes algorithm was applied to the segmented data to produce two detailed, compatible isosurfaces, one for blood and one for tissue. Both isosurfaces were simultaneously smoothed with a multimaterial smoothing algorithm that exactly conserves the volume for each phase. Using these two isosurfaces, we developed and applied novel automated meshing algorithms to generate anisotropic hybrid meshes on arbitrary biological geometries with the number of layers and the desired element anisotropy for each phase as the only input parameters. Since our meshes adapt to the local feature sizes and include boundary layer prisms, they are more efficient and accurate than non-adaptive, isotropic meshes, and the fluid-structure interaction computations will tend to have relative error equilibrated over the whole mesh.

Indexed as

Models, CardiovascularAlgorithmsAnimalsComputer SimulationCoronary CirculationHeartImage EnhancementImage Interpretation, Computer-AssistedImaging, Three-DimensionalMagnetic Resonance AngiographyMaleMiceMice, Inbred C57BLReproducibility of ResultsRheologySensitivity and Specificity

Identifiers

PMID19727874
PMCPMC2837787

What OpenQuestion holds

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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.