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Clinical Considerations of Coagulopathy in Acute Liver Failure

Acute liver failure (ALF) is the rapid onset of severe liver dysfunction, defined by the presence of hepatic encephalopathy and impaired synthetic function (international normalized ratio of ≥1.5) in the absence of underlying liver disease. The elevated international normalized ratio value in ALF is...

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Autores principales: Kim, Ahyoung, Niu, Bolin, Woreta, Tinsay, Chen, Po-Hung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: XIA & HE Publishing Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782116/
https://www.ncbi.nlm.nih.gov/pubmed/33447524
http://dx.doi.org/10.14218/JCTH.2020.00058
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author Kim, Ahyoung
Niu, Bolin
Woreta, Tinsay
Chen, Po-Hung
author_facet Kim, Ahyoung
Niu, Bolin
Woreta, Tinsay
Chen, Po-Hung
author_sort Kim, Ahyoung
collection PubMed
description Acute liver failure (ALF) is the rapid onset of severe liver dysfunction, defined by the presence of hepatic encephalopathy and impaired synthetic function (international normalized ratio of ≥1.5) in the absence of underlying liver disease. The elevated international normalized ratio value in ALF is often misinterpreted as an increased hemorrhagic tendency, which can lead to inappropriate, prophylactic transfusions of blood products. However, global assessments of coagulopathy via viscoelastic tests or thrombin generation assay suggest a reestablished hemostatic, or even hypercoagulable, status in patients with ALF. Although the current versions of global assays are not perfect, they can provide more nuanced insights into the hemostatic system in ALF than the conventional measures of coagulopathy.
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spelling pubmed-77821162021-01-13 Clinical Considerations of Coagulopathy in Acute Liver Failure Kim, Ahyoung Niu, Bolin Woreta, Tinsay Chen, Po-Hung J Clin Transl Hepatol Review Article Acute liver failure (ALF) is the rapid onset of severe liver dysfunction, defined by the presence of hepatic encephalopathy and impaired synthetic function (international normalized ratio of ≥1.5) in the absence of underlying liver disease. The elevated international normalized ratio value in ALF is often misinterpreted as an increased hemorrhagic tendency, which can lead to inappropriate, prophylactic transfusions of blood products. However, global assessments of coagulopathy via viscoelastic tests or thrombin generation assay suggest a reestablished hemostatic, or even hypercoagulable, status in patients with ALF. Although the current versions of global assays are not perfect, they can provide more nuanced insights into the hemostatic system in ALF than the conventional measures of coagulopathy. XIA & HE Publishing Inc. 2020-10-10 2020-12-28 /pmc/articles/PMC7782116/ /pubmed/33447524 http://dx.doi.org/10.14218/JCTH.2020.00058 Text en © 2020 Authors. http://creativecommons.org/licenses/by-nc/4.0/ This article has been published under the terms of Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0), which permits noncommercial unrestricted use, distribution, and reproduction in any medium, provided that the following statement is provided. “This article has been published in Journal of Clinical and Translational Hepatology at DOI: 10.14218/JCTH.2020.00058 and can also be viewed on the Journal’s website at http://www.jcthnet.com”.
spellingShingle Review Article
Kim, Ahyoung
Niu, Bolin
Woreta, Tinsay
Chen, Po-Hung
Clinical Considerations of Coagulopathy in Acute Liver Failure
title Clinical Considerations of Coagulopathy in Acute Liver Failure
title_full Clinical Considerations of Coagulopathy in Acute Liver Failure
title_fullStr Clinical Considerations of Coagulopathy in Acute Liver Failure
title_full_unstemmed Clinical Considerations of Coagulopathy in Acute Liver Failure
title_short Clinical Considerations of Coagulopathy in Acute Liver Failure
title_sort clinical considerations of coagulopathy in acute liver failure
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782116/
https://www.ncbi.nlm.nih.gov/pubmed/33447524
http://dx.doi.org/10.14218/JCTH.2020.00058
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