Management of Portal vein Thrombosis in Cirrhosis

被引:2
作者
Meena, Babu Lal [1 ]
Sarin, Shiv Kumar [1 ]
机构
[1] Inst Liver & Biliary Sci, Dept Hepatol, D-1 Vasant Kunj, New Delhi 110070, India
关键词
thrombosis; EHPVO; portal hypertension; anticoagulants; TIPS; INTRAHEPATIC PORTOSYSTEMIC SHUNT; DIRECT ORAL ANTICOAGULANTS; LIVER-TRANSPLANTATION; RISK-FACTORS; CLINICAL-OUTCOMES; VARICEAL BLEED; EFFICACY; SAFETY; DISEASE; THERAPY;
D O I
10.1055/s-0044-1791247
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Portal vein thrombosis (PVT) is one of the common complications of cirrhosis. The incidence of PVT correlates with liver disease severity-higher incidence in patients with Child-Turcotte-Pugh (CTP) C, large spontaneous portosystemic shunts, hepatofugal portal flow, and in the presence of hepatocellular carcinoma. PVT may worsen ascites, increase the risk and poor control of variceal bleeding. The occurrence of PVT may increase morbidity and lower survival after a liver transplant. Using statins prevents the occurrence of PVT, whereas beta-blockers may aggravate its occurrence. Cross-sectional imaging is mandatory for the precise diagnosis and classification of PVT. Symptomatic, occlusive PVT and candidacy for liver transplantation are the main indications for anticoagulation. Vitamin K antagonists, low-molecular-weight heparin, and newer anticoagulants are effective and safe in cirrhosis. Direct-acting oral anticoagulants are agents of choice in early cirrhosis (CTP A, B). The duration of anticoagulant therapy, predictors of response, and management of complications of cirrhosis while on therapy require in-depth knowledge and individualized treatment. Transjugular intrahepatic porto-systemic shunt can be considered in nonresponsive cases or when anticoagulants are contraindicated. This manuscript reviews the latest updated knowledge about managing PVT in cirrhosis.
引用
收藏
页码:416 / 429
页数:14
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