Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity
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Univ Arizona, Dept Med & Biomed EngnIssue Date
2019-02-27
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NATURE PUBLISHING GROUPCitation
Chiu, W. C., Tran, P. L., Khalpey, Z., Lee, E., Woo, Y. R., Slepian, M. J., & Bluestein, D. (2019). Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity. Scientific reports, 9(1), 2946.Journal
SCIENTIFIC REPORTSRights
© The Author(s) 2019. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Ventricular assist devices (VAD), a mainstay of therapy for advanced and end-stage heart failure, remain plagued by device thrombogenicity. Combining advanced in silico and in vitro methods, Device Thrombogenicity Emulation (DTE) is a device design approach for enhancing VAD thromboresistance. Here we tested DTE efficacy in experimental VAD designs. DTE incorporates iterative design modifications with advanced CFD to compute the propensity of large populations of platelets to activate by flow-induced stresses (statistically representing the VAD 'Thrombogenic Footprint'). The DTE approach was applied to a VAD (MINDTE) design with a favorable thromboresistance profile and compared against a design (MAXDTE) that generated an intentionally poor thromboresistance profile. DTE predictions were confirmed by testing physical prototypes in vitro by measuring VAD thrombogenicity using the modified prothrombinase assay. Chronic in vivo studies in VAD implanted calves, revealed MINDTE calf surviving well with low platelet activation, whereas the MAXDTE animal sustained thromboembolic strokes. DTE predictions were confirmed, correlating with in vitro and in vivo thrombogenicity, supporting utility in guiding device development, potentially reducing the need for animal studies.Note
Open access journal.ISSN
2045-2322PubMed ID
30814674Version
Final published versionSponsors
National Institute of Biomedical Imaging and Bioengineering [EB008004, 1U01EB012487]Additional Links
https://www.nature.com/articles/s41598-019-39897-6ae974a485f413a2113503eed53cd6c53
10.1038/s41598-019-39897-6
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Except where otherwise noted, this item's license is described as © The Author(s) 2019. Open Access. This article is licensed under a Creative Commons Attribution 4.0 International License.
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