Evidence map›Paper›PMID 27156141›Full record

ArticleBiomaterials2016

Visualization and analysis of biomaterial-centered thrombus formation within a defined crevice under flow.

Megan A Jamiolkowski, Drake D Pedersen, Wei-Tao Wu, James F Antaki, William R Wagner

Abstract read
In one paragraph

Article in Biomaterials, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  4. Influence of Hematocrit Level and Integrin αCellular and molecular bioengineering · 2024
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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

5 authors.

Megan A JamiolkowskiMcGowan Institute for Regenerative Medicine, Pittsburgh, PA, USA; Dept. of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.
Drake D PedersenMcGowan Institute for Regenerative Medicine, Pittsburgh, PA, USA; Dept. of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA.
Wei-Tao WuDept. of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA, USA.
James F AntakiDept. of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA; Dept. of Biomedical Engineering, Carnegie Mellon University, Pittsburgh, PA, USA.
William R WagnerMcGowan Institute for Regenerative Medicine, Pittsburgh, PA, USA; Dept. of Bioengineering, University of Pittsburgh, Pittsburgh, PA, USA; Dept. of Surgery, University of Pittsburgh, Pittsburgh, PA, USA; Dept. of Chemical Engineering, University of Pittsburgh, Pittsburgh, PA, USA. Electronic address: wagnerwr@upmc.edu.

Funding

Multiscale Model of Thrombosis in Artificial CirculationR01HL089456 · NHLBI · CORNELL UNIVERSITY · PI ANTAKI, JAMES F., BUTCHER, JONATHAN TALBOT · 2009 to 2024
$8.5M
Cardiovascular Bioengineering Training ProgramT32HL076124 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SANJEEV G SHROFF · 2005 to 2026
$7.0M
Cellular Approaches to Tissue Engineering/RegenerationT32EB001026 · NIBIB · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DUNCAN, ANDREW W, MONGA, SATDARSHAN SINGH · 2003 to 2024
$5.5M
NHLBI NIH HHS R01 HL089456NHLBI NIH HHS T32 HL076124NIBIB NIH HHS T32 EB001026
6 · The paper itself

Abstract

The blood flow pathway within a device, together with the biomaterial surfaces and status of the patient's blood, are well-recognized factors in the development of thrombotic deposition and subsequent embolization. Blood flow patterns are of particular concern for devices such as blood pumps (i.e. ventricular assist devices, VADs) where shearing forces can be high, volumes are relatively large, and the flow fields can be complex. However, few studies have examined the effect of geometric irregularities on thrombus formation on clinically relevant opaque materials under flow. The objective of this study was to quantify human platelet deposition onto Ti6Al4V alloys, as well as positive and negative control surfaces, in the region of defined crevices (∼50-150 μm in width) that might be encountered in many VADs or other cardiovascular devices. To achieve this, reconstituted fresh human blood with hemoglobin-depleted red blood cells (to achieve optical clarity while maintaining relevant rheology), long working optics, and a custom designed parallel plate flow chamber were employed. The results showed that the least amount of platelet deposition occurred in the largest crevice size examined, which was counterintuitive. The greatest levels of deposition occurred in the 90 μm and 53 μm crevices at the lower wall shear rate. The results suggest that while crevices may be unavoidable in device manufacturing, the crevice size might be tailored, depending on the flow conditions, to reduce the risk of thromboembolic events. Further, these data might be used to improve the accuracy of predictive models of thrombotic deposition in cardiovascular devices to help optimize the blood flow path and reduce device thrombogenicity.

Indexed as

RheologyAdultBiocompatible MaterialsComputer SimulationComputer SystemsFemaleHumansMalePerfusionPlatelet AdhesivenessProbabilityThrombosisBiocompatible MaterialsCrevicesDisturbed flowMicroscopyPlateletsRed blood cell ghostsThrombosis

Identifiers

PMID27156141
PMCPMC4982661

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.