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Measuring the anticoagulant effect of low molecular weight heparins in the critically ill

Antithrombotic prophylaxis in critically ill patients frequently fails. Venous thromboembolism is associated with adverse clinical outcomes, including a prolonged intensive care unit stay and death. A potential mechanism by which critically ill patients may be predisposed to antithrombotic failure i...

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Detalles Bibliográficos
Autores principales: Crowther, Mark, Lim, Wendy
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1751004/
https://www.ncbi.nlm.nih.gov/pubmed/16879730
http://dx.doi.org/10.1186/cc4978
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author Crowther, Mark
Lim, Wendy
author_facet Crowther, Mark
Lim, Wendy
author_sort Crowther, Mark
collection PubMed
description Antithrombotic prophylaxis in critically ill patients frequently fails. Venous thromboembolism is associated with adverse clinical outcomes, including a prolonged intensive care unit stay and death. A potential mechanism by which critically ill patients may be predisposed to antithrombotic failure is the inability to achieve 'prophylactic' anticoagulant drug levels as a result of impaired absorption. For example, previous studies have shown that patients on inotropes have reduced serum levels of low molecular weight heparin, presumably on the basis of reduced absorption from the subcutaneous injection site. In the previous issue of the journal, Rommers and colleagues examined whether subcutaneous edema reduces absorption of a low molecular weight heparin; although small, and thus underpowered, the authors failed to find any relationship between the level of low molecular weight heparin and the presence of edema. These findings provide reassurance that subcutaneously administered medications may be used in critically ill patients with edema.
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spelling pubmed-17510042006-12-27 Measuring the anticoagulant effect of low molecular weight heparins in the critically ill Crowther, Mark Lim, Wendy Crit Care Commentary Antithrombotic prophylaxis in critically ill patients frequently fails. Venous thromboembolism is associated with adverse clinical outcomes, including a prolonged intensive care unit stay and death. A potential mechanism by which critically ill patients may be predisposed to antithrombotic failure is the inability to achieve 'prophylactic' anticoagulant drug levels as a result of impaired absorption. For example, previous studies have shown that patients on inotropes have reduced serum levels of low molecular weight heparin, presumably on the basis of reduced absorption from the subcutaneous injection site. In the previous issue of the journal, Rommers and colleagues examined whether subcutaneous edema reduces absorption of a low molecular weight heparin; although small, and thus underpowered, the authors failed to find any relationship between the level of low molecular weight heparin and the presence of edema. These findings provide reassurance that subcutaneously administered medications may be used in critically ill patients with edema. BioMed Central 2006 2006-07-25 /pmc/articles/PMC1751004/ /pubmed/16879730 http://dx.doi.org/10.1186/cc4978 Text en Copyright © 2006 BioMed Central Ltd
spellingShingle Commentary
Crowther, Mark
Lim, Wendy
Measuring the anticoagulant effect of low molecular weight heparins in the critically ill
title Measuring the anticoagulant effect of low molecular weight heparins in the critically ill
title_full Measuring the anticoagulant effect of low molecular weight heparins in the critically ill
title_fullStr Measuring the anticoagulant effect of low molecular weight heparins in the critically ill
title_full_unstemmed Measuring the anticoagulant effect of low molecular weight heparins in the critically ill
title_short Measuring the anticoagulant effect of low molecular weight heparins in the critically ill
title_sort measuring the anticoagulant effect of low molecular weight heparins in the critically ill
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1751004/
https://www.ncbi.nlm.nih.gov/pubmed/16879730
http://dx.doi.org/10.1186/cc4978
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