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Endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation

A heparin-like effect was recently described in infants, children, and adults receiving bivalirudin while supported on extracorporeal membrane oxygenation following cardiopulmonary bypass. This is most likely due to endogenous release of glycosaminoglycans from vascular endothelium and mast cells an...

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Autores principales: MacLaren, Graeme, Monagle, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318132/
https://www.ncbi.nlm.nih.gov/pubmed/25629374
http://dx.doi.org/10.1186/s13054-014-0636-4
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author MacLaren, Graeme
Monagle, Paul
author_facet MacLaren, Graeme
Monagle, Paul
author_sort MacLaren, Graeme
collection PubMed
description A heparin-like effect was recently described in infants, children, and adults receiving bivalirudin while supported on extracorporeal membrane oxygenation following cardiopulmonary bypass. This is most likely due to endogenous release of glycosaminoglycans from vascular endothelium and mast cells and is associated with longer duration of extracorporeal membrane oxygenation and an increased incidence of sepsis. Further investigation into this effect should include patients without recent cardiopulmonary bypass, exclude the presence of covalent antithrombin-heparin complexes, and employ a variety of different heparinases for thromboelastography. The phenomenon may partially explain the heterogeneity of anticoagulation requirements in patients on extracorporeal life support.
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spelling pubmed-43181322015-02-06 Endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation MacLaren, Graeme Monagle, Paul Crit Care Commentary A heparin-like effect was recently described in infants, children, and adults receiving bivalirudin while supported on extracorporeal membrane oxygenation following cardiopulmonary bypass. This is most likely due to endogenous release of glycosaminoglycans from vascular endothelium and mast cells and is associated with longer duration of extracorporeal membrane oxygenation and an increased incidence of sepsis. Further investigation into this effect should include patients without recent cardiopulmonary bypass, exclude the presence of covalent antithrombin-heparin complexes, and employ a variety of different heparinases for thromboelastography. The phenomenon may partially explain the heterogeneity of anticoagulation requirements in patients on extracorporeal life support. BioMed Central 2014-11-21 2014 /pmc/articles/PMC4318132/ /pubmed/25629374 http://dx.doi.org/10.1186/s13054-014-0636-4 Text en © MacLaren and Monagle; licensee BioMed Central Ltd. 2014 The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Commentary
MacLaren, Graeme
Monagle, Paul
Endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation
title Endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation
title_full Endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation
title_fullStr Endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation
title_full_unstemmed Endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation
title_short Endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation
title_sort endogenous glycosaminoglycan anticoagulation in extracorporeal membrane oxygenation
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318132/
https://www.ncbi.nlm.nih.gov/pubmed/25629374
http://dx.doi.org/10.1186/s13054-014-0636-4
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