Why the study?
The utilization and long-term treatment persistence of DOACs among patients with nonvalvular atrial fibrillation and liver disease needed characterization.
Are direct oral anticoagulants associated with higher long-term treatment persistence compared to vitamin K antagonists in patients with nonvalvular atrial fibrillation and liver disease?
Are direct oral anticoagulants associated with higher long-term treatment persistence compared to vitamin K antagonists in patients with nonvalvular atrial fibrillation and liver disease?
In patients with NVAF and liver disease, DOACs are more frequently initiated than VKAs and are associated with higher, though still relatively low, 5-year treatment persistence.
Low DOAC persistence in NVAF with liver disease warrants monitoring; leaves open need for adherence interventions in this population.
AIMS: We characterized the utilization and long-term treatment persistence of direct oral anticoagulants (DOACs) in patients with nonvalvular atrial fibrillation (NVAF) and liver disease. METHOD: Using the UK Clinical Practice Research Datalink, we assembled a population-based cohort of NVAF patients with liver disease initiating oral anticoagulants between 2011 and 2020. Logistic regression estimated odds ratios (ORs) and 95% confidence intervals (CIs) of the association between patient characteristics and initiation of DOACs vs vitamin K antagonists (VKAs). Cox proportional hazards models estimated hazard ratios (HRs) and 95% CIs of the association between patient characteristics and the switch from VKAs to DOACs vs remaining on VKAs. We also assessed the 5-year treatment persistence with DOACs vs VKAs, and whether ischemic stroke or bleeding preceded treatment discontinuation. RESULTS: Our cohort included 3167 NVAF patients with liver disease initiating DOACs (n = 2247, 71%) or VKAs (n = 920, 29%). Initiators of DOACs were more likely to have prior ischemic stroke (OR 1.44, 95% CI 1.12-1.85) than VKA initiators but less likely to have used antiplatelet agents (OR 0.66, 95% CI 0.53-0.82). Patients switching to DOACs were more likely to have used selective serotonin reuptake inhibitors (HR 1.64, 95% CI 1.13-2.37) than those remaining on VKAs. At 5 years, 31% of DOAC initiators and 9% of VKA initiators remained persistent. Only few patients were diagnosed with ischemic stroke or bleeding prior to treatment discontinuation. CONCLUSION: Most NVAF patients with liver disease initiated treatment with DOACs. Long-term persistence with DOACs was higher than with VKAs but remained relatively low.
No takes yet. Share an insight, caveat, or question.
Douros et al. (2021) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: