Effectiveness of Edoxaban in Portal Vein Thrombosis Associated with Liver Cirrhosis

Author:

Tadokoro Tomoko1,Tani Joji1,Manabe Takushi1,Takuma Kei1,Nakahara Mai1,Oura Kyoko1,Mimura Shima1,Fujita Koji1,Nomura Takako2,Morishita Asahiro1,Kobara Hideki1,Himoto Takashi3,Ono Masafumi4,Masaki Tsutomu1

Affiliation:

1. Department of Gastroenterology and Neurology, Kagawa University School of Medicine

2. Gastroenterology and Hepatology, HITO Medical Center

3. Department of Medical Technology, Kagawa Prefectural University of Health Sciences

4. Division of Innovative Medicine for Hepatobiliary and Pancreatology, Faculty of Medicine, Kagawa University School of Medicine

Abstract

Abstract Portal vein thrombosis (PVT) worsens the long-term prognosis of patients with cirrhosis; however, the optimal treatment remains to be determined. Reports on the efficacy of direct oral anticoagulants are increasing, and further evidence is needed. Therefore, we investigated the effectiveness of treatment with edoxaban in patients with PVT. We retrospectively reviewed the outcomes of edoxaban and warfarin as antithrombotic therapies for PVT. The median overall survival time was 4.2 years in patients with PVT, with a 1-year survival rate of 70.7% and a 5-year survival rate of 47.9%. The leading cause of death was hepatocellular carcinoma. Compared to warfarin, edoxaban significantly improved PVT. In addition, edoxaban provided long-term improvement of PVT. Warfarin, on the other hand, was temporarily effective but did not provide long-term benefits. The Child-Pugh and albumin-bilirubin scores did not change after edoxaban or warfarin use. No deaths occurred due to adverse events associated with edoxaban or warfarin. Edoxaban as a single agent can achieve long-term thrombolysis without compromising the hepatic reserves. Edoxaban is easy to initiate, even in an outpatient setting, and could become a major therapeutic agent for the treatment of PVT.

Publisher

Research Square Platform LLC

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