Comparing Safety and Efficacy of Direct Oral Anticoagulants Versus Warfarin in Extreme Obesity

Background Limited clinical data exists regarding use of direct oral anticoagulants (DOACs) in extreme obesity, specifically those >= 140 kg or having a body mass index (BMI) >= 50 kg/m(2). Objective Evaluate the safety and efficacy of DOACs in extreme obesity. Patients/Methods A retrospective chart review was performed at a single center of patients aged 18-89 years and weight >= 140 kg or BMI >= 50 kg/m(2) receiving warfarin or DOAC therapy. Patients were followed for 1 year from prescribing/study inclusion. The primary outcome was the difference in rates of any bleed (composite of major, nonmajor clinically relevant, or minor bleeding events as defined by International Society of Thrombosis and Haemostasis (ISTH) criteria) between groups. Secondary outcomes included individual components of the composite primary outcome and effectiveness in preventing thrombotic events within 12 months. Post-hoc multivariate analysis evaluated potential predictors of bleeding events within overall patient population. Results Two-hundred eighty-five patients were included, 80 and 205 in the DOAC and warfarin groups, respectively. Rates of any documented bleeding event were comparable in DOAC and warfarin groups (17.5% vs 17.1%, P > .05). No significant difference in rates of minor (P = .067), nonmajor clinically relevant (P = .825), and major (P = 1) bleeding events were observed. Two thrombotic events occurred in the warfarin group compared to none in the DOAC group. Increasing weight was associated with bleeding events in multivariate analysis. Conclusions This data did not demonstrate a difference in safety or efficacy outcomes between DOACs and warfarin when utilized in patients with extreme obesity.