Key result
Warfarin shows conflicting mortality associations vs DOACs across UK and Hong Kong cohorts.
Why the study?
Differences in the hazard of all-cause mortality associated with warfarin compared with DOAC may depend in part on anticoagulation control in warfarin users.
Does warfarin alter the risk of all-cause mortality compared to DOACs in adults with non-valvular atrial fibrillation?
Cohort
Yes
Does warfarin alter the risk of all-cause mortality compared to DOACs in adults with non-valvular atrial fibrillation?
The comparative mortality risk between warfarin and DOACs in non-valvular atrial fibrillation is highly dependent on the quality of warfarin anticoagulation control (time in therapeutic range).
TTR may modify mortality differences between warfarin and DOACs; hypothesis-generating and should not yet change practice.
BACKGROUND: Direct oral anticoagulants (DOACs) have been reported to be associated with a higher risk of mortality compared with an older alternative, warfarin using primary care data in the United Kingdom (UK). However, other studies observed contradictory findings. We therefore aimed to investigate the association between mortality and warfarin, compared with DOACs. METHODS: We conducted cohort studies using UK Clinical Practice Research Datalink (CPRD) Aurum and Hong Kong Clinical Data Analysis and Reporting System (CDARS) to identify the association between warfarin and hazard of mortality, compared to DOACs. Individuals with non-valvular atrial fibrillation aged ≥ 18 years who had first anticoagulant therapy (warfarin or DOAC) during 1/1/2011-31/12/2019 were included. RESULTS: Compared with DOAC use, a lower hazard of all-cause mortality was found in warfarin users (hazard ratio (HR) = 0.81, 95% confidence interval (CI) = 0.77-0.86) in CPRD; while a higher hazard was observed in warfarin users (HR = 1.31, 95% CI = 1.24-1.39) in CDARS, versus DOAC users. In our exploratory analysis, consistent results were seen in both databases when stratified warfarin users by time in therapeutic range (TTR) using post-baseline measurements: a lower hazard of all-cause mortality in warfarin users with TTR ≥ 65% (CPRD: HR = 0.68, 95% CI = 0.65-0.72; CDARS: HR = 0.86, 95% CI = 0.77-0.96) and increased hazard in warfarin users with TTR < 65% (CPRD: HR = 1.14, 95% CI = 1.05-1.23; CDARS: HR = 1.59, 95% CI = 1.50-1.69), versus DOAC users. CONCLUSIONS: The differences in hazard of all-cause mortality associated with warfarin compared with DOAC, in part may depend on anticoagulation control in warfarin users. Notably, this study is unable to establish a causal relationship between warfarin and mortality stratified by TTR, versus DOACs, requiring future studies for further investigation.
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Wang et al. (2024) conducted a cohort in non-valvular atrial fibrillation. Warfarin vs. Direct oral anticoagulants (DOACs) was evaluated on all-cause mortality (HR 0.81, 95% CI 0.77-0.86). Compared with DOACs, warfarin was associated with a lower hazard of all-cause mortality in the UK database (HR 0.81; 95% CI 0.77-0.86) but a higher hazard in the Hong Kong database (HR 1.31).
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