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Portal vein thrombosis in cirrhosis: Why a well-known complication is still matter of debate

Portal vein thrombosis (PVT) represents a well-known complication during the natural course of liver cirrhosis (LC), ranging from asymptomatic cases to life-threating conditions related to portal hypertension and hepatic decompensation. Portal flow stasis, complex acquired hypercoagulable disorders...

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Autores principales: Faccia, Mariella, Ainora, Maria Elena, Ponziani, Francesca Romana, Riccardi, Laura, Garcovich, Matteo, Gasbarrini, Antonio, Pompili, Maurizio, Zocco, Maria Assunta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710174/
https://www.ncbi.nlm.nih.gov/pubmed/31496623
http://dx.doi.org/10.3748/wjg.v25.i31.4437
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author Faccia, Mariella
Ainora, Maria Elena
Ponziani, Francesca Romana
Riccardi, Laura
Garcovich, Matteo
Gasbarrini, Antonio
Pompili, Maurizio
Zocco, Maria Assunta
author_facet Faccia, Mariella
Ainora, Maria Elena
Ponziani, Francesca Romana
Riccardi, Laura
Garcovich, Matteo
Gasbarrini, Antonio
Pompili, Maurizio
Zocco, Maria Assunta
author_sort Faccia, Mariella
collection PubMed
description Portal vein thrombosis (PVT) represents a well-known complication during the natural course of liver cirrhosis (LC), ranging from asymptomatic cases to life-threating conditions related to portal hypertension and hepatic decompensation. Portal flow stasis, complex acquired hypercoagulable disorders and exogenous factors leading to endothelial dysfunction have emerged as key factors for PVT development. However, PVT occurrence remains unpredictable and many issues regarding its natural history, prognostic significance and treatment are still elusive. In particular although spontaneous resolution or disease stability occur in most cases of PVT, factors predisposing to disease progression or recurrence after spontaneous recanalization are not clarified as yet. Moreover, PVT impact on LC outcome is still debated, as PVT may represent itself a consequence of liver fibrosis and hepatic dysfunction progression. Anticoagulation and transjugular intrahepatic portosystemic shunt are considered safe and effective in this setting and are recommended in selected cases, even if the safer therapeutic option and the optimal therapy duration are still unknown. Nevertheless, their impact on mortality rates should be addressed more extensively. In this review we present the most debated questions regarding PVT, whose answers should come from prospective cohort studies and large sample-size randomized trials.
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spelling pubmed-67101742019-09-06 Portal vein thrombosis in cirrhosis: Why a well-known complication is still matter of debate Faccia, Mariella Ainora, Maria Elena Ponziani, Francesca Romana Riccardi, Laura Garcovich, Matteo Gasbarrini, Antonio Pompili, Maurizio Zocco, Maria Assunta World J Gastroenterol Minireviews Portal vein thrombosis (PVT) represents a well-known complication during the natural course of liver cirrhosis (LC), ranging from asymptomatic cases to life-threating conditions related to portal hypertension and hepatic decompensation. Portal flow stasis, complex acquired hypercoagulable disorders and exogenous factors leading to endothelial dysfunction have emerged as key factors for PVT development. However, PVT occurrence remains unpredictable and many issues regarding its natural history, prognostic significance and treatment are still elusive. In particular although spontaneous resolution or disease stability occur in most cases of PVT, factors predisposing to disease progression or recurrence after spontaneous recanalization are not clarified as yet. Moreover, PVT impact on LC outcome is still debated, as PVT may represent itself a consequence of liver fibrosis and hepatic dysfunction progression. Anticoagulation and transjugular intrahepatic portosystemic shunt are considered safe and effective in this setting and are recommended in selected cases, even if the safer therapeutic option and the optimal therapy duration are still unknown. Nevertheless, their impact on mortality rates should be addressed more extensively. In this review we present the most debated questions regarding PVT, whose answers should come from prospective cohort studies and large sample-size randomized trials. Baishideng Publishing Group Inc 2019-08-21 2019-08-21 /pmc/articles/PMC6710174/ /pubmed/31496623 http://dx.doi.org/10.3748/wjg.v25.i31.4437 Text en ©The Author(s) 2019. 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 Minireviews
Faccia, Mariella
Ainora, Maria Elena
Ponziani, Francesca Romana
Riccardi, Laura
Garcovich, Matteo
Gasbarrini, Antonio
Pompili, Maurizio
Zocco, Maria Assunta
Portal vein thrombosis in cirrhosis: Why a well-known complication is still matter of debate
title Portal vein thrombosis in cirrhosis: Why a well-known complication is still matter of debate
title_full Portal vein thrombosis in cirrhosis: Why a well-known complication is still matter of debate
title_fullStr Portal vein thrombosis in cirrhosis: Why a well-known complication is still matter of debate
title_full_unstemmed Portal vein thrombosis in cirrhosis: Why a well-known complication is still matter of debate
title_short Portal vein thrombosis in cirrhosis: Why a well-known complication is still matter of debate
title_sort portal vein thrombosis in cirrhosis: why a well-known complication is still matter of debate
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710174/
https://www.ncbi.nlm.nih.gov/pubmed/31496623
http://dx.doi.org/10.3748/wjg.v25.i31.4437
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