Anticoagulation for Atrial Fibrillation in Patients with Decompensated Liver Cirrhosis: Bold and Brave?

Author:

Gîrleanu Irina12ORCID,Trifan Anca12ORCID,Huiban Laura12,Muzica Cristina Maria12ORCID,Petrea Oana Cristina12,Sîngeap Ana-Maria12ORCID,Cojocariu Camelia12ORCID,Chiriac Stefan12ORCID,Cuciureanu Tudor12ORCID,Stafie Remus12ORCID,Zenovia Sebastian12ORCID,Stratina Ermina12ORCID,Rotaru Adrian12ORCID,Nastasa Robert12ORCID,Sfarti Catalin12ORCID,Costache Irina Iuliana13,Stanciu Carol12

Affiliation:

1. Department of Gastroenterology, “Grigore T. Popa” University of Medicine and Pharmacy, 700115 Iasi, Romania

2. Institute of Gastroenterology and Hepatology, “Saint Spiridon” University Hospital, 700111 Iasi, Romania

3. Cardiology Department, “Saint Spiridon” University Hospital, 700115 Iasi, Romania

Abstract

Atrial fibrillation is frequently diagnosed in patients with liver cirrhosis, especially in those with non-alcoholic steatohepatitis or alcoholic etiology. Anticoagulant treatment is recommended for thromboembolic protection in patients with atrial fibrillation. Considering the impaired coagulation balance in liver cirrhosis, predisposing patients to bleed or thrombotic events, the anticoagulant treatment is still a matter of debate. Although patients with liver cirrhosis were excluded from the pivotal studies that confirmed the efficacy and safety of the anticoagulant treatment in patients with atrial fibrillation, data from real-life cohorts demonstrated that the anticoagulant treatment in patients with liver cirrhosis could be safe. This review aimed to evaluate the recent data regarding the safety and efficacy of anticoagulant treatment in patients with decompensated liver cirrhosis. Direct oral anticoagulants are safer than warfarin in patients with compensated liver cirrhosis. In Child–Pugh class C liver cirrhosis, direct oral anticoagulants are contraindicated. New bleeding and ischemic risk scores should be developed especially for patients with liver cirrhosis, and biomarkers for bleeding complications should be implemented in clinical practice to personalize this treatment in a very difficult population represented by decompensated liver cirrhosis patients.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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