In vitro thrombogenicity testing of pulsatile mechanical circulatory support systems: Design and proof-of-concept.

mechanical circulatory support mock circulatory loop porcine blood pulsatile mechanical circulatory support thromboelastometry thrombogenicity

Journal

Artificial organs
ISSN: 1525-1594
Titre abrégé: Artif Organs
Pays: United States
ID NLM: 7802778

Informations de publication

Date de publication:
Dec 2021
Historique:
revised: 21 06 2021
received: 16 03 2021
accepted: 12 07 2021
pubmed: 28 7 2021
medline: 19 1 2022
entrez: 27 7 2021
Statut: ppublish

Résumé

Thrombogenic complications are a main issue in mechanical circulatory support (MCS). There is no validated in vitro method available to quantitatively assess the thrombogenic performance of pulsatile MCS devices under realistic hemodynamic conditions. The aim of this study is to propose a method to evaluate the thrombogenic potential of new designs without the use of complex in-vivo trials. This study presents a novel in vitro method for reproducible thrombogenicity testing of pulsatile MCS systems using low molecular weight heparinized porcine blood. Blood parameters are continuously measured with full blood thromboelastometry (ROTEM; EXTEM, FIBTEM and a custom-made analysis HEPNATEM). Thrombus formation is optically observed after four hours of testing. The results of three experiments are presented each with two parallel loops. The area of thrombus formation inside the MCS device was reproducible. The implantation of a filter inside the loop catches embolizing thrombi without a measurable increase of platelet activation, allowing conclusions of the place of origin of thrombi inside the device. EXTEM and FIBTEM parameters such as clotting velocity (α) and maximum clot firmness (MCF) show a total decrease by around 6% with a characteristic kink after 180 minutes. HEPNATEM α and MCF rise within the first 180 minutes indicate a continuously increasing activation level of coagulation. After 180 minutes, the consumption of clotting factors prevails, resulting in a decrease of α and MCF. With the designed mock loop and the presented protocol we are able to identify thrombogenic hot spots inside a pulsatile pump and characterize their thrombogenic potential.

Identifiants

pubmed: 34312890
doi: 10.1111/aor.14046
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1513-1521

Informations de copyright

© 2021 The Authors. Artificial Organs published by International Center for Artificial Organ and Transplantation and Wiley Periodicals LLC.

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Auteurs

Moritz K Brockhaus (MK)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Medical Faculty, RWTH Aachen University, Aachen, Germany.

Mehdi J Behbahani (MJ)

Biomaterials Laboratory, Institute of Bioengineering, Aachen University of Applied Sciences, Campus Jülich, Aachen, Germany.

Farina Muris (F)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Medical Faculty, RWTH Aachen University, Aachen, Germany.

Sebastian V Jansen (SV)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Medical Faculty, RWTH Aachen University, Aachen, Germany.

Thomas Schmitz-Rode (T)

Institute of Applied Medical Engineering, Medical Faculty, RWTH Aachen University, Aachen, Germany.

Ulrich Steinseifer (U)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Medical Faculty, RWTH Aachen University, Aachen, Germany.

Johanna C Clauser (JC)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Medical Faculty, RWTH Aachen University, Aachen, Germany.

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