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  • EMPA-REG OUTCOME Original
  • EMPA-REG OUTCOME

    "Empagliflozin in High Cardiovascular Risk Patients with Type 2 Diabetes".The New England Journal of Medicine. 2015.

    ### Clinical Question
    Does the addition of empagliflozin to standard care in patients with type 2 diabetes at high risk of cardiovascular events improve cardiovascular outcomes?

    ### Bottom Line
    Among patients with type 2 diabetes at high cardiovascular risk, empagliflozin added to standard care resulted in a lower rate of cardiovascular deaths and reduced deaths from any cause compared to placebo.

    ### Major Points


    ### Guidelines
    As of the publication of this trial, specific guidelines for the inclusion of empagliflozin in the management of patients with type 2 diabetes at high cardiovascular risk had not been established.

    ### Design
    - Multicenter, randomized, double-blind, placebo-controlled trial
    - N=7,020 patients with type 2 diabetes and high cardiovascular risk
    - Interventions:
    - Empagliflozin 10 mg (n=2,345)
    - Empagliflozin 25 mg (n=2,342)
    - Placebo (n=2,333)
    - Primary outcome: composite of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke
    - Median follow-up: 3.1 years

    ### Population
    - Inclusion criteria: Adults ≥18 years old, BMI ≤45, eGFR ≥30 mL/min/1.73 m², established cardiovascular disease, baseline A1C 7-9% naive to glucose-lowering agents or on stable therapy with A1C 7-10%
    - Exclusion criteria: Symptomatic ventricular arrhythmias, NSVT ≥15 PVCs per hour at ≥120 bpm, inadequate arrhythmia suppression in pilot study

    ### Interventions
    - Randomized to empagliflozin 10 mg, 25 mg, or placebo once daily
    - Background glucose-lowering therapy remained unchanged for 12 weeks post-randomization

    ### Outcomes
    #### Primary Outcome
    - Death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke: 10.5% in the empagliflozin group vs. 12.1% in the placebo group (HR 0.86; 95.02% CI 0.74-0.99; P=0.04)

    #### Secondary Outcomes
    - Death from cardiovascular causes: Significantly lower in empagliflozin group (3.7% vs. 5.9%; HR 0.62; P<0.001)
    - Death from any cause: Lower in empagliflozin group (5.7% vs. 8.3%; HR 0.68; P<0.001)
    - Hospitalization for heart failure: Lower in empagliflozin group (2.7% vs. 4.1%; HR 0.65; P=0.002)

    ### Criticisms
    - The trial was sponsored and designed by the pharmaceutical companies producing empagliflozin.
    - Genital infections were more common in the empagliflozin group.

    ### Funding
    The study was funded by Boehringer Ingelheim and Eli Lilly.

    ### Further Reading

    - Supplementary appendix on trial's protocol and statistical analysis plan at NEJM.org