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A fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas

Over the past decade, much of the development of computational models of device-related thrombosis has focused on platelet activity. While those models have been successful in predicting thrombus formation in medical devices operating at high shear rates (> 5000 s(−1)), they cannot be directly ap...

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Autores principales: Méndez Rojano, Rodrigo, Lai, Angela, Zhussupbekov, Mansur, Burgreen, Greg W., Cook, Keith, Antaki, James F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560616/
https://www.ncbi.nlm.nih.gov/pubmed/36190991
http://dx.doi.org/10.1371/journal.pcbi.1010277
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author Méndez Rojano, Rodrigo
Lai, Angela
Zhussupbekov, Mansur
Burgreen, Greg W.
Cook, Keith
Antaki, James F.
author_facet Méndez Rojano, Rodrigo
Lai, Angela
Zhussupbekov, Mansur
Burgreen, Greg W.
Cook, Keith
Antaki, James F.
author_sort Méndez Rojano, Rodrigo
collection PubMed
description Over the past decade, much of the development of computational models of device-related thrombosis has focused on platelet activity. While those models have been successful in predicting thrombus formation in medical devices operating at high shear rates (> 5000 s(−1)), they cannot be directly applied to low-shear devices, such as blood oxygenators and catheters, where emerging information suggest that fibrin formation is the predominant mechanism of clotting and platelet activity plays a secondary role. In the current work, we augment an existing platelet-based model of thrombosis with a partial model of the coagulation cascade that includes contact activation of factor XII and fibrin production. To calibrate the model, we simulate a backward-facing-step flow channel that has been extensively characterized in-vitro. Next, we perform blood perfusion experiments through a microfluidic chamber mimicking a hollow fiber membrane oxygenator and validate the model against these observations. The simulation results closely match the time evolution of the thrombus height and length in the backward-facing-step experiment. Application of the model to the microfluidic hollow fiber bundle chamber capture both gross features such as the increasing clotting trend towards the outlet of the chamber, as well as finer local features such as the structure of fibrin around individual hollow fibers. Our results are in line with recent findings that suggest fibrin production, through contact activation of factor XII, drives the thrombus formation in medical devices operating at low shear rates with large surface area to volume ratios.
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spelling pubmed-95606162022-10-14 A fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas Méndez Rojano, Rodrigo Lai, Angela Zhussupbekov, Mansur Burgreen, Greg W. Cook, Keith Antaki, James F. PLoS Comput Biol Research Article Over the past decade, much of the development of computational models of device-related thrombosis has focused on platelet activity. While those models have been successful in predicting thrombus formation in medical devices operating at high shear rates (> 5000 s(−1)), they cannot be directly applied to low-shear devices, such as blood oxygenators and catheters, where emerging information suggest that fibrin formation is the predominant mechanism of clotting and platelet activity plays a secondary role. In the current work, we augment an existing platelet-based model of thrombosis with a partial model of the coagulation cascade that includes contact activation of factor XII and fibrin production. To calibrate the model, we simulate a backward-facing-step flow channel that has been extensively characterized in-vitro. Next, we perform blood perfusion experiments through a microfluidic chamber mimicking a hollow fiber membrane oxygenator and validate the model against these observations. The simulation results closely match the time evolution of the thrombus height and length in the backward-facing-step experiment. Application of the model to the microfluidic hollow fiber bundle chamber capture both gross features such as the increasing clotting trend towards the outlet of the chamber, as well as finer local features such as the structure of fibrin around individual hollow fibers. Our results are in line with recent findings that suggest fibrin production, through contact activation of factor XII, drives the thrombus formation in medical devices operating at low shear rates with large surface area to volume ratios. Public Library of Science 2022-10-03 /pmc/articles/PMC9560616/ /pubmed/36190991 http://dx.doi.org/10.1371/journal.pcbi.1010277 Text en © 2022 Méndez Rojano et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Méndez Rojano, Rodrigo
Lai, Angela
Zhussupbekov, Mansur
Burgreen, Greg W.
Cook, Keith
Antaki, James F.
A fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas
title A fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas
title_full A fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas
title_fullStr A fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas
title_full_unstemmed A fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas
title_short A fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas
title_sort fibrin enhanced thrombosis model for medical devices operating at low shear regimes or large surface areas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9560616/
https://www.ncbi.nlm.nih.gov/pubmed/36190991
http://dx.doi.org/10.1371/journal.pcbi.1010277
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