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  3. Antithrombotic treatment with direct-acting oral anticoagulants in patients with splanchnic vein thrombosis and cirrhosis.

Antithrombotic treatment with direct-acting oral anticoagulants in patients with splanchnic vein thrombosis and cirrhosis.

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DOI
10.7892/boris.93571
Publisher DOI
10.1111/liv.13285
PubMed ID
27778440
Abstract
BACKGROUND

Direct-acting oral anticoagulants (DOACs) are used in patients with splanchnic vein thrombosis (SVT) and cirrhosis, but evidence for safety and efficacy in this setting is limited. Our aim was to identify indications and reasons for starting or switching to DOACs and to report adverse effects, complications and short-term outcome.

METHODS

Data collection including demographic information, laboratory values, treatment and complications through the Vascular Liver Disease Interest Group Consortium.

RESULTS

Forty-five centres (90%) of the consortium completed the initial eCRF. We report here a series of 94 patients from 17 centres. Thirty-six patients (38%) had cirrhosis. Child-Pugh score was 6 (range 5-8), and MELD score 10.2 (range 6-19). Indications for anticoagulation were splanchnic vein thrombosis (75%), deep vein thrombosis (5%), atrial fibrillation (14%) and others (6%). DOACs used were rivaroxaban (83%), dabigatran (11%) and apixaban (6%). Patients were followed up for a median duration of 15 months (cirrhotic) and 26.5 months (non-cirrhotic). Adverse events occurred in 17% of patients and included one case of recurrent portal vein thrombosis and five cases of bleeding. Treatment with DOACs was stopped in three cases. The major reasons for choosing DOACs were no need for monitoring or inadequacy of INR to guide anticoagulation in cirrhotic patients. Renal and liver function did not change during treatment.

CONCLUSIONS

A consistent number of patients with SVT and/or cirrhosis are currently treated with DOACs, which seem to be effective and safe. These data provide a basis for performing randomized clinical trials of DOACs vs. low molecular weight heparin or vitamin K antagonists.
Date Issued
2017-05
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Subjects
Budd-Chiari syndrome
•
anticoagulation
•
cirrhosis
•
portal vein thrombosis
Language(s)
en
Author(s)
De Gottardi, Andrea  
Universitätsklinik für Viszerale Chirurgie und Medizin, Hepatologie  
Departement Klinische Forschung, Hepatologie Forschung  
Trebicka, Jonel
Klinger, Christoph
Plessier, Aurélie
Seijo, Susana
Terziroli, Benedetta
Magenta, Lorenzo
Semela, David
Buscarini, Elisabetta
Langlet, Philippe
Görtzen, Jan
Puente, Angela
Müllhaupt, Beat
Navascuès, Carmen
Nery, Filipe
Deltenre, Pierre
Turon, Fanny
Engelmann, Cornelius
Arya, Rupen
Caca, Karel
Peck-Radosavljevic, Markus
Leebeek, Frank W G
Valla, Dominique
Garcia-Pagan, Juan Carlos
Additional Credits
Departement Klinische Forschung, Hepatologie Forschung  
Universitätsklinik für Viszerale Chirurgie und Medizin, Hepatologie  
Journal
Liver international
Publisher
Wiley
ISSN
1478-3223
Access(Rights)
restricted
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