Table 3.
End points of the EMPA-REG OUTCOME Trial
Outcome | Hazard Ratio Compared with Placebo (95% CI) |
---|---|
Prespecified | |
Primary MACE (CV death, nonfatal MI, or nonfatal stroke) | 0.86 (0.74 to 0.99) |
CV death | 0.62 (0.49 to 0.77) |
All-cause mortality | 0.68 (0.57 to 0.82) |
Hospitalization for heart failure | 0.65 (0.50 to 0.85) |
Exploratory | |
New onset of macroalbuminuria | 0.62 (0.54 to 0.72) |
New onset or worsening of DKD | 0.61 (0.53 to 0.70) |
Doubling of serum creatininea | 0.56 (0.39 to 0.79) |
Initiation of RRT | 0.45 (0.21 to 0.97) |
Created with data from the supplemental appendix of the Randomized, Placebo-Controlled Cardiovascular Outcome Trial of Empaglifozin (EMPA-REG OUTCOME) (5,6). At baseline, the study population had an average eGFR of approximately 74 ml/min per 1.73 m2. 95% CI, 95% confidence interval; MACE, major adverse cardiovascular event; CV, cardiovascular; MI, myocardial infarction; DKD, diabetic kidney disease.
Accompanied by eGFR≤45 ml/min per 1.73 m2.