4.5 Review

Efficacy and safety of direct oral anticoagulants versus vitamin K antagonist for portal vein thrombosis in cirrhosis: A systematic review and meta-analysis

Journal

DIGESTIVE AND LIVER DISEASE
Volume 54, Issue 1, Pages 56-62

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.dld.2021.07.039

Keywords

Cirrhosis; Direct oral anticoagulation; Portal vein thrombosis

Funding

  1. Nurturing Clinician Scientist Scheme (NCCS) award by SingHealth Duke-NUS Academic Medical center
  2. National Medical Research Council Singapore

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This study aimed to compare the efficacy and safety of DOAC versus VKA in treating non-tumoral PVT in cirrhotic patients. The results showed that DOAC were associated with higher PVT recanalization rate, but had similar bleeding risk compared to VKA.
Introduction and aim: Portal vein thrombosis (PVT) is associated with a higher risk of liver-related com-plications. Recent guidelines recommend direct-acting anticoagulants (DOAC) in patients with cirrhosis and non-tumoral PVT. However, data on the efficacy and safety of DOAC in these patients remain limited. We aim to investigate the efficacy and safety of DOAC compared to vitamin K antagonists (VKA) to treat non-tumoral PVT in patients with cirrhosis. Methods: We performed a systematic search of six electronic databases using MeSH term and free text. We selected all studies comparing the use of DOACs with vitamin K antagonist to treat PVT in cirrho-sis. The primary outcome was PVT recanalization. Secondary outcomes were and PVT progression, major bleeding, variceal bleeding and death. Results: From 944 citations, we included 552 subjects from a total of 11 studies (10 observational and 1 randomized trial) that fulfilled the inclusion criteria. We found that DOAC were associated with a higher pooled rate of PVT recanalization (RR = 1.67, 95%CI: 1.02, 2.74, I 2 = 79%) and lower pooled risk of PVT progression (RR = 0.14, 95%CI: 0.03-0.57, I 2 = 0%). The pooled risk of major bleeding (RR = 0.29, 95%CI: 0.08-1.01, I 2 = 0%), variceal bleeding (RR = 1.29, 95%CI: 0.64-2.59, I 2 = 0%) and death (RR = 0.31, 95%CI: 0.01-9.578, I 2 = 80%) was similar between DOAC and VKA. Conclusion: For the treatment of PVT in patients with cirrhosis, the bleeding risk was comparable be-tween DOAC and VKA. However, DOAC were associated with a higher pooled rate of PVT recanalization. Dedicated randomized studies are needed to confirm these findings. (c) 2021 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.

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