Why the study?
Patients with AF and decompensated cirrhosis have limited evidence to guide DOAC drug selection or dosing due to exclusion from pivotal trials and uncertain safety and effectiveness.
Observational
Propensity-matched study evaluates bleeding and thromboembolic outcomes in atrial fibrillation with decompensated cirrhosis, indicating the impact of DOAC selection and dosing.
Patients with atrial fibrillation (AF) and decompensated cirrhosis represent a high-risk population for anticoagulation, characterized by simultaneous susceptibility to thromboembolic and bleeding complications due to a rebalanced but unstable hemostatic state. These patients have been largely excluded from pivotal randomized trials of direct oral anticoagulants (DOACs), leaving limited evidence to guide drug selection or dosing in advanced liver disease.1,2 Although observational studies in the general AF population consistently demonstrate lower rates of major bleeding with apixaban compared with rivaroxaban, it remains unclear whether this advantage extends to patients with decompensated cirrhosis or whether reduced-dose DOAC regimens offer comparable safety and effectiveness to standard dosing in this setting.
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Zanco et al. (2026) conducted an observational in Atrial fibrillation with decompensated cirrhosis. Direct oral anticoagulants was evaluated.
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