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Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity

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...

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Autores principales: Chiu, Wei Che, Tran, Phat L., Khalpey, Zain, Lee, Eric, Woo, Yi-Ren, Slepian, Marvin J., Bluestein, Danny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393420/
https://www.ncbi.nlm.nih.gov/pubmed/30814674
http://dx.doi.org/10.1038/s41598-019-39897-6
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author Chiu, Wei Che
Tran, Phat L.
Khalpey, Zain
Lee, Eric
Woo, Yi-Ren
Slepian, Marvin J.
Bluestein, Danny
author_facet Chiu, Wei Che
Tran, Phat L.
Khalpey, Zain
Lee, Eric
Woo, Yi-Ren
Slepian, Marvin J.
Bluestein, Danny
author_sort Chiu, Wei Che
collection PubMed
description 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 (MIN(DTE)) design with a favorable thromboresistance profile and compared against a design (MAX(DTE)) 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 MIN(DTE) calf surviving well with low platelet activation, whereas the MAX(DTE) 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.
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spelling pubmed-63934202019-03-01 Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity Chiu, Wei Che Tran, Phat L. Khalpey, Zain Lee, Eric Woo, Yi-Ren Slepian, Marvin J. Bluestein, Danny Sci Rep Article 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 (MIN(DTE)) design with a favorable thromboresistance profile and compared against a design (MAX(DTE)) 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 MIN(DTE) calf surviving well with low platelet activation, whereas the MAX(DTE) 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. Nature Publishing Group UK 2019-02-27 /pmc/articles/PMC6393420/ /pubmed/30814674 http://dx.doi.org/10.1038/s41598-019-39897-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chiu, Wei Che
Tran, Phat L.
Khalpey, Zain
Lee, Eric
Woo, Yi-Ren
Slepian, Marvin J.
Bluestein, Danny
Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity
title Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity
title_full Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity
title_fullStr Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity
title_full_unstemmed Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity
title_short Device Thrombogenicity Emulation: An In Silico Predictor of In Vitro and In Vivo Ventricular Assist Device Thrombogenicity
title_sort device thrombogenicity emulation: an in silico predictor of in vitro and in vivo ventricular assist device thrombogenicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6393420/
https://www.ncbi.nlm.nih.gov/pubmed/30814674
http://dx.doi.org/10.1038/s41598-019-39897-6
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