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Portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture

Portal vein thrombosis (PVT) is a frequent and serious complication in patients with liver cirrhosis (LC). Recently, a new classification of PVT was proposed, although the functional component was not completed included. The status of liver disease (compensated/decompensated) should be added to this...

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Autores principales: Gîrleanu, Irina, Trifan, Anca, Stanciu, Carol, Sfarti, Cătălin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196341/
https://www.ncbi.nlm.nih.gov/pubmed/30356984
http://dx.doi.org/10.3748/wjg.v24.i39.4419
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author Gîrleanu, Irina
Trifan, Anca
Stanciu, Carol
Sfarti, Cătălin
author_facet Gîrleanu, Irina
Trifan, Anca
Stanciu, Carol
Sfarti, Cătălin
author_sort Gîrleanu, Irina
collection PubMed
description Portal vein thrombosis (PVT) is a frequent and serious complication in patients with liver cirrhosis (LC). Recently, a new classification of PVT was proposed, although the functional component was not completed included. The status of liver disease (compensated/decompensated) should be added to this classification. Reduced portal flow velocity and the acquired hypercoagulable status associated with LC are the main risk factors for PVT development, although endothelial dysfunction may play an important role that needs to be further evaluated. The European Association for the Study of the Liver and the American Association for the Study of Liver Disease recommend that the anticoagulant treatment should be consider in cirrhotic patients with PVT. Low molecular weight heparin and vitamin K antagonists proved their efficacy and relatively safety in PVT treatment, although in addition to recanalization rates, more complex end-points such as mortality and decompensation rate should be evaluated. The new oral anticoagulant therapies offers the advantage of oral administration in the absence of laboratory monitoring, however, there are a few reports regarding their use in cirrhotic patients, most of them referring to compensated isolated cases. Transjugular intrahepatic portosystemic shunt could be an alternative if thrombosis progresses despite anticoagulatant therapy and/or when PVT is associated with portal hypertension complications. The aim of this editorial is to discuss the different aspects of pathophysiology, clinical relevance, diagnosis and management of PVT in patients with LC.
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spelling pubmed-61963412018-10-23 Portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture Gîrleanu, Irina Trifan, Anca Stanciu, Carol Sfarti, Cătălin World J Gastroenterol Editorial Portal vein thrombosis (PVT) is a frequent and serious complication in patients with liver cirrhosis (LC). Recently, a new classification of PVT was proposed, although the functional component was not completed included. The status of liver disease (compensated/decompensated) should be added to this classification. Reduced portal flow velocity and the acquired hypercoagulable status associated with LC are the main risk factors for PVT development, although endothelial dysfunction may play an important role that needs to be further evaluated. The European Association for the Study of the Liver and the American Association for the Study of Liver Disease recommend that the anticoagulant treatment should be consider in cirrhotic patients with PVT. Low molecular weight heparin and vitamin K antagonists proved their efficacy and relatively safety in PVT treatment, although in addition to recanalization rates, more complex end-points such as mortality and decompensation rate should be evaluated. The new oral anticoagulant therapies offers the advantage of oral administration in the absence of laboratory monitoring, however, there are a few reports regarding their use in cirrhotic patients, most of them referring to compensated isolated cases. Transjugular intrahepatic portosystemic shunt could be an alternative if thrombosis progresses despite anticoagulatant therapy and/or when PVT is associated with portal hypertension complications. The aim of this editorial is to discuss the different aspects of pathophysiology, clinical relevance, diagnosis and management of PVT in patients with LC. Baishideng Publishing Group Inc 2018-10-21 2018-10-21 /pmc/articles/PMC6196341/ /pubmed/30356984 http://dx.doi.org/10.3748/wjg.v24.i39.4419 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Editorial
Gîrleanu, Irina
Trifan, Anca
Stanciu, Carol
Sfarti, Cătălin
Portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture
title Portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture
title_full Portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture
title_fullStr Portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture
title_full_unstemmed Portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture
title_short Portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture
title_sort portal vein thrombosis in cirrhotic patients - it is always the small pieces that make the big picture
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196341/
https://www.ncbi.nlm.nih.gov/pubmed/30356984
http://dx.doi.org/10.3748/wjg.v24.i39.4419
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