Summary
Dabigatran is approved for stroke risk reduction in patients with nonvalvular atrial
fibrillation (NVAF). Data from diverse clinical practice settings will help establish
whether the risk:benefit ratio seen in clinical trials is comparable with routine
clinical care. This study aimed to compare the safety and effectiveness of dabigatran
and warfarin in clinical practice. We undertook a propensity score-matched (PSM) cohort
study (N=12,793 per group; mean age 74) comparing treatment with dabigatran or warfarin
in the US Department of Defense claims database, October 2009 to July 2013. Treatment-naïve
patients with first prescription claim for dabigatran (either FDA-approved dose) or
warfarin between October 2010 and July 2012 (index) and a diagnosis of NVAF during
the 12 months before index date were included. Primary outcomes were stroke and major
bleeding. Secondary outcomes included ischaemic and haemorrhagic stroke, major gastrointestinal
(GI), urogenital or other bleeding, myocardial infarction (MI) and death. Time-to-event
was investigated using Kaplan-Meier survival analyses. Outcomes comparisons were made
utilising Cox-proportional hazards models of PSM groups. Dabigatran users experienced
fewer strokes (adjusted hazard ratio [95 % confidence intervals] 0.73 [0.55–0.97]),
major intracranial (0.49 [0.30–0.79]), urogenital (0.36 [0.18–0.74]) and other (0.38
[0.22–0.66]) bleeding, MI (0.65 [0.45–0.95]) and deaths (0.64 [0.55–0.74]) than the
warfarin group. Major bleeding (0.87 [0.74–1.03]) and major GI bleeding (1.13 [0.94–1.37])
was similar between groups and major lower GI bleeding events were more frequent (1.30
[1.04–1.62]) with dabigatran. In conclusion, compared with warfarin, dabigatran treatment
was associated with a lower risk of stroke and most outcomes measured, but increased
incidence of major lower GI bleeding.
Keywords
Atrial fibrillation - anticoagulant - stroke - stroke prevention - bleeding