# EASL postgraduate course report: Vascular biology in chronic liver disease and clinical management implications

**Authors:** Pierre-Emmanuel Rautou, Ton Lisman, Virginia Hernandez-Gea, Cristina Ripoll

PMC · DOI: 10.1016/j.jhepr.2025.101399 · 2025-03-19

## TL;DR

This paper summarizes a postgraduate course on vascular biology in chronic liver disease, focusing on hemostasis, vascular disorders, and complications like portal hypertension.

## Contribution

The paper provides updated insights into managing vascular complications in cirrhosis and introduces the redefined concept of porto-sinusoidal vascular disorder.

## Key findings

- Haemostatic changes in cirrhosis require careful management to avoid bleeding without routinely correcting lab abnormalities.
- Porto-sinusoidal vascular disorder is a newly redefined condition encompassing multiple histological and clinical patterns.
- Non-invasive identification of clinically significant portal hypertension is now possible, and TIPS indications have expanded.

## Abstract

This article reviews the content of the EASL Congress 2024 postgraduate course on vascular biology in chronic liver disease and its clinical management. It focuses on haemostasis in patients with cirrhosis, vascular liver diseases including porto-sinusoidal vascular disorder and portal vein thrombosis, and portal hypertension and its extrahepatic complications in cirrhosis. Haemostatic changes in cirrhosis coincide with complex shifts between the risks of bleeding and thrombosis, making management decisions challenging. Importantly, laboratory test abnormalities should not be routinely corrected to avoid bleeding. Regarding vascular liver diseases, the term porto-sinusoidal vascular disorder is a recently redefined entity encompassing various overlapping histological patterns (e.g. nodular regenerative hyperplasia, obliterative portal venopathy) and clinical entities (e.g. idiopathic portal hypertension). These disorders have in common the absence of cirrhosis together with vascular alterations in the porto-sinusoidal region and/or feature(s) of portal hypertension. The management of portal vein thrombosis varies according to the presence or absence of cirrhosis. Anticoagulation is increasingly used in this setting and portal vein recanalisation using interventional radiology techniques is an attractive approach. Paradigms on cirrhosis-associated portal hypertension have evolved in recent years: prevention of decompensation in compensated patients has become a prime objective, non-invasive identification of patients with clinically significant portal hypertension has become possible, the concept of “recompensation” in decompensated patients has been proposed, and indications for TIPS (transjugular intrahepatic portosystemic shunts) have been progressively expanded. Extrahepatic vascular complications of cirrhosis include portopulmonary hypertension, hepatopulmonary syndrome, hepatorenal syndrome, and cirrhotic cardiomyopathy. Each of these complications poses unique challenges that affect liver disease management and transplant eligibility, underscoring the need for specialised care.

## Linked entities

- **Diseases:** cirrhosis (MONDO:0005155), portal vein thrombosis (MONDO:0001339), portal hypertension (MONDO:0005080), portopulmonary hypertension (MONDO:0017154), hepatopulmonary syndrome (MONDO:0004694), hepatorenal syndrome (MONDO:0001382), cirrhotic cardiomyopathy (MONDO:0018932)

## Full-text entities

- **Diseases:** obliterative portal venopathy (MESH:C538011), hepatopulmonary syndrome (MESH:D020065), vascular complications (MESH:D003925), portopulmonary hypertension (MESH:D006973), chronic liver disease (MESH:D008107), portal hypertension (MESH:D006975), nodular regenerative hyperplasia (MESH:D020518), portal vein thrombosis (MESH:D012170), cirrhotic cardiomyopathy (MESH:D009202), idiopathic portal hypertension (MESH:D000094724), bleeding (MESH:D006470), hepatorenal syndrome (MESH:D006530), cirrhosis (MESH:D005355), thrombosis (MESH:D013927)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12284368/full.md

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Source: https://tomesphere.com/paper/PMC12284368