Background The ENSURE‐AF study (NCT 02072434) of anticoagulation for electrical cardioversion in nonvalvular atrial fibrillation (NVAF) showed comparable low rates of bleeding and thromboembolism between the edoxaban and the enoxaparin‐warfarin… Click to show full abstract
Background The ENSURE‐AF study (NCT 02072434) of anticoagulation for electrical cardioversion in nonvalvular atrial fibrillation (NVAF) showed comparable low rates of bleeding and thromboembolism between the edoxaban and the enoxaparin‐warfarin treatment arms. This post hoc analysis investigated the relationship between renal function and clinical outcomes. Methods ENSURE‐AF was a multicenter, PROBE evaluation trial of edoxaban 60 mg, or dose reduced to 30 mg/d for weight ≤60 kg, creatinine clearance (CrCl; Cockcroft‐Gault) ≤50 mL/min, or concomitant P‐glycoprotein inhibitors compared with therapeutically monitored enoxaparin‐warfarin in 2,199 NVAF patients undergoing electrical cardioversion. Efficacy and safety outcomes and time in therapeutic range in the warfarin arm were analyzed in relation to CrCl in prespecified ranges ≥15 and ≤30, >30 and ≤50, >50 and <80, and ≥80 mL/min, and an exploratory ≥95‐mL/min analysis. Results A total of 1,095 subjects were randomized to edoxaban and 1,104 to enoxaparin‐warfarin. Mean age was 64.3 ± 10 and 64.2 ± 11 years. Mean time in therapeutic range was progressively lower with reducing CrCl strata, being 66.8% in those with CrCl >30 to ≤50 compared with 71.8% in those with CrCl ≥80. The odds ratios for the primary efficacy and safety end points were comparable for the different predefined renal function strata; given the small numbers, the 95% CI included 1.0. In the subset of those with CrCl ≥95, the odds ratios showed consistency with the other CrCl strata. When CrCl was assessed as a continuous variable, there was a nonsignificant trend toward higher major or clinically relevant nonmajor bleeding with reducing CrCl levels, with no significant differences between the 2 treatment arms. When we assessed CrCl at baseline compared with end of treatment, there were no significant differences in CrCl change between the edoxaban and enoxaparin‐warfarin arms. The proportions with worsening of renal function (defined as a decrease of >20% from baseline) were similar in the 2 treatment arms. Conclusion Given the small number of events in ENSURE‐AF, no effect of renal (dys)function was demonstrated in comparing edoxaban to enoxaparin‐warfarin for cardioversion; efficacy and safety of edoxaban remained consistent even in patients with normal or supranormal renal function.
               
Click one of the above tabs to view related content.