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Viscoelastometry to Manage Bleeding in Liver Disease

A state of “re-balanced haemostasis” describes complex coagulation changes that arise in patients with liver disease. Changes include alterations in procoagulant and anticoagulant proteins, platelets and von Willebrand factor, as well as the fibrinolytic system. Various circumstances including infec...

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Autores principales: Wilson, Samantha, Joseph, Joanne, Danta, Mark, Rabbolini, David J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402654/
https://www.ncbi.nlm.nih.gov/pubmed/37546051
http://dx.doi.org/10.7759/cureus.41401
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author Wilson, Samantha
Joseph, Joanne
Danta, Mark
Rabbolini, David J
author_facet Wilson, Samantha
Joseph, Joanne
Danta, Mark
Rabbolini, David J
author_sort Wilson, Samantha
collection PubMed
description A state of “re-balanced haemostasis” describes complex coagulation changes that arise in patients with liver disease. Changes include alterations in procoagulant and anticoagulant proteins, platelets and von Willebrand factor, as well as the fibrinolytic system. Various circumstances including infection, trauma, or surgery may disrupt this balance and predispose an individual to bleeding or thrombosis. The prothrombin time, international normalised ratio, and activated partial thromboplastin time are conventional coagulation screening tests that are routinely employed by clinicians to investigate unexplained bleeding, monitor anticoagulation, and inform preoperative assessments of bleeding risk. These standard coagulation tests assess quantitative defects in procoagulant clotting factors and are insensitive to levels of natural anticoagulants, which together with procoagulant factors, are often perturbed in liver disease. Therefore, the prolongation of clotting times measured by these tests often does not reflect the multifaceted alterations of haemostasis in these patients. Viscoelastic testing (VET) provides a more encompassing assessment of clotting function by recording real-time viscoelastic changes in whole blood and includes parameters that provide information on coagulation factor function, platelet contribution to clot formation, as well as fibrinolysis. To date, VET has been employed to predict and inform transfusion support in obstetric, trauma, and cardiac surgical fields, and its use in patients undergoing liver transplantation is well established. The ability of VET to accurately predict bleeding risk and precisely guide transfusion algorithms for patients with liver disease undergoing other invasive procedures or experiencing bleeding complications has been the topic of research over the last decade. This review is a critical summary of this data and provides a detailed snapshot of the position of VET as a clinical tool in patients with liver disease.
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spelling pubmed-104026542023-08-05 Viscoelastometry to Manage Bleeding in Liver Disease Wilson, Samantha Joseph, Joanne Danta, Mark Rabbolini, David J Cureus Gastroenterology A state of “re-balanced haemostasis” describes complex coagulation changes that arise in patients with liver disease. Changes include alterations in procoagulant and anticoagulant proteins, platelets and von Willebrand factor, as well as the fibrinolytic system. Various circumstances including infection, trauma, or surgery may disrupt this balance and predispose an individual to bleeding or thrombosis. The prothrombin time, international normalised ratio, and activated partial thromboplastin time are conventional coagulation screening tests that are routinely employed by clinicians to investigate unexplained bleeding, monitor anticoagulation, and inform preoperative assessments of bleeding risk. These standard coagulation tests assess quantitative defects in procoagulant clotting factors and are insensitive to levels of natural anticoagulants, which together with procoagulant factors, are often perturbed in liver disease. Therefore, the prolongation of clotting times measured by these tests often does not reflect the multifaceted alterations of haemostasis in these patients. Viscoelastic testing (VET) provides a more encompassing assessment of clotting function by recording real-time viscoelastic changes in whole blood and includes parameters that provide information on coagulation factor function, platelet contribution to clot formation, as well as fibrinolysis. To date, VET has been employed to predict and inform transfusion support in obstetric, trauma, and cardiac surgical fields, and its use in patients undergoing liver transplantation is well established. The ability of VET to accurately predict bleeding risk and precisely guide transfusion algorithms for patients with liver disease undergoing other invasive procedures or experiencing bleeding complications has been the topic of research over the last decade. This review is a critical summary of this data and provides a detailed snapshot of the position of VET as a clinical tool in patients with liver disease. Cureus 2023-07-05 /pmc/articles/PMC10402654/ /pubmed/37546051 http://dx.doi.org/10.7759/cureus.41401 Text en Copyright © 2023, Wilson et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Gastroenterology
Wilson, Samantha
Joseph, Joanne
Danta, Mark
Rabbolini, David J
Viscoelastometry to Manage Bleeding in Liver Disease
title Viscoelastometry to Manage Bleeding in Liver Disease
title_full Viscoelastometry to Manage Bleeding in Liver Disease
title_fullStr Viscoelastometry to Manage Bleeding in Liver Disease
title_full_unstemmed Viscoelastometry to Manage Bleeding in Liver Disease
title_short Viscoelastometry to Manage Bleeding in Liver Disease
title_sort viscoelastometry to manage bleeding in liver disease
topic Gastroenterology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402654/
https://www.ncbi.nlm.nih.gov/pubmed/37546051
http://dx.doi.org/10.7759/cureus.41401
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