Portal vein thrombosis: diagnosis, management, and endpoints for future clinical studies

ERN RARE-LIVER and VALDIG, an EASL consortium, Laure Elkrief, Virginia Hernandez-Gea, Marco Senzolo, Agustin Albillos, Anna Baiges, Annalisa Berzigotti, Christophe Bureau, Sarwa Darwish Murad, Andrea De Gottardi, François Durand, Juan Carlos Garcia-Pagan, Ton Lisman, Mattias Mandorfer, Valérie McLin, Lucile Moga, Filipe Nery, Patrick Northup, Alexandre Nuzzo, Valérie ParadisDavid Patch, Audrey Payancé, Vincent Plaforet, Aurélie Plessier, Johanne Poisson, Lara Roberts, Riad Salem, Shiv Sarin, Akash Shukla, Christian Toso, Dhiraj Tripathi, Dominique Valla, Maxime Ronot, Pierre Emmanuel Rautou*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

8 Citations (Scopus)

Abstract

Portal vein thrombosis (PVT) refers to the development of a non-malignant obstruction of the portal vein, its branches, its radicles, or a combination. This Review first provides a comprehensive overview of all aspects of PVT, namely the specifics of the portal venous system, the risk factors for PVT, the pathophysiology of portal hypertension in PVT, the interest in non-invasive tests, as well as therapeutic approaches including the effect of treating risk factors for PVT or cause of cirrhosis, anticoagulation, portal vein recanalisation by interventional radiology, and prevention and management of variceal bleeding in patients with PVT. Specific issues are also addressed including portal cholangiopathy, mesenteric ischaemia and intestinal necrosis, quality of life, fertility, contraception and pregnancy, and PVT in children. This Review will then present endpoints for future clinical studies in PVT, both in patients with and without cirrhosis, agreed by a large panel of experts through a Delphi consensus process. These endpoints include classification of portal vein thrombus extension, classification of PVT evolution, timing of assessment of PVT, and global endpoints for studies on PVT including clinical outcomes. These endpoints will help homogenise studies on PVT and thus facilitate reporting, comparison between studies, and validation of future studies and trials on PVT.

Original languageEnglish
Pages (from-to)859-883
Number of pages25
JournalThe Lancet Gastroenterology and Hepatology
Volume9
Issue number9
DOIs
Publication statusPublished - Sept-2024

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