Abstract
Portal vein thrombosis (PVT) is a well-known complication of liver diseases; however, still much has to be done to improve the knowledge and treatment of this condition. Relevant methodological flaws have led to controversial results and many questions remain unanswered. Prospective, controlled quality studies are strongly required to advance in this field. PVT development prediction using scores, biomarkers or viscoelastic tests are promising emerging topics but a research planning on data collection and validation strategy should be defined. Direct oral anti-coagulants (DOACs) seem to be safe and effective in the treatment of PVT, but prospective randomized controlled data are lacking as well as indication about length of therapy and stopping rules. Future lines of research should focus not only on avoidance of thrombosis but also on exploring the extended role of anticoagulation as anti-inflammatory and antifibrotic intervention.
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Abbreviations
- DOAC:
-
Direct oral anti-coagulants
- HCC:
-
Hepatocellular carcinoma
- LMWH:
-
Low molecular weight heparin
- LT:
-
Liver transplantation
- PVT:
-
Portal vein thrombosis
- TIPS:
-
Transjugular intrahepatic portosystemic shunt
- US:
-
UltraSonography
- VTE:
-
Venous thrombo-embolism
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Bianchini, M., Villa, E. (2021). Future Directions. In: Qi, X., Xie, W. (eds) Portal Vein Thrombosis. Springer, Singapore. https://doi.org/10.1007/978-981-33-6538-4_12
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