which occurred in 130 patients in the edoxaban group(3.2%) and 146 patients in the warfarin group (3.5%) (hazard ratio, 0.89; 95% confidenceinterval [CI], 0.70 to 1.13; P<0.001 for noninferiority). The safety outcomeoccurred in 349 patients (8.5%) in the edoxaban group and 423 patients (10.3%) inthe warfarin group (hazard ratio, 0.81; 95% CI, 0.71 to 0.94; P = 0.004 for superiority).The rates of other adverse events were similar in the two groups. A total of 938 patientswith pulmonary embolism had right ventricular dysfunction, as assessed bymeasurement of N-terminal pro–brain natriuretic peptide levels; the rate of recurrentvenous thromboembolism in this subgroup was 3.3% in the edoxaban groupand 6.2% in the warfarin group (hazard ratio, 0.52; 95% CI, 0.28 to 0.98).
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