Bleeding in anticoagulated patients with AF: practical considerations 47 controlled trials (RCTs), NOACs reduced the risk of stroke or SE by 19% compared with warfarin (relative risk [RR], 0.81; 95% CI, 0.73-0.91), large ly due to a markedly lower rate of hemorrhagic strokes (RR 0.49, 95% CI, 0.38-0.64) and intracra nial bleeding (ICB) (RR, 0.48; 95% CI, 0.39-0.59). 9 However, the use of NOACs (in particular, full dose dabigatran and rivaroxaban) was signifi cantly associated with an increased risk of gas trointestinal (GI) bleeding (RR, 1.25; 95% CI, 1.01-1.55). 7 Of note, the differences between baseline stroke and bleeding risks among differ ent NOAC trials could have affected the report ed bleeding rates (FIguRE 1). Residual incidence of stroke or SE despite NOAC use among pa tients with AF is estimated at 1.5% to 2.5% per year and that of major bleeding at 2% to 4% per year. 9 As compared with warfarin, NOACs slight ly reduced all cause mortality (RR, 0.89; 95% CI, 0.85-0.94), vascular mortality (RR, 0.88; 95% CI, 0.82-0.94), and bleeding related mortality (RR, 0.54; 95% CI, 0.44-0.67). 10 Importantly, in the phase 3 AF trials, NOACs were more effective than warfarin in the prevention of stroke or SE among patients with AF aged 75 years or older.