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Deutsches Zentrum für Herzinsuffizienz Würzburg
Comprehensive Heart Failure Center

Am Schwarzenberg 15
Haus A15
97078 Würzburg

Tel.: (+49)931-201-46333
Fax: (+49)931-201-646333
Email: dzhi@ukw.de

Für Patienten: (+49)931-201-46301

BMBF Förderkennzeichen:
bis 1.11.15: 01EO1004
ab  1.11.15: 01EO1504

Publikation des Monats - Januar 2016

Christoph Wanner, David Fitchett, Bernard Zinman et al

>> Heart failure outcomes with empagliflozin in patients with type 2 diabetes at high cardiovascular risk: results of the EMPA-REG OUTCOME® trial

Eur Heart J 2015;37,7

Aims

We previously reported that in the EMPA-REG OUTCOMEw trial, empagliflozin added to standard of care reduced the risk of 3-point major adverse cardiovascular events, cardiovascular and all-cause death, and hospitalization for heart failure in patients with type 2 diabetes and high cardiovascular risk. We have now further investigated heart failure outcomes in all patients and in subgroups, including patients with or without baseline heart failure.

Methods and results

Patients were randomized to receive empagliflozin 10 mg, empagliflozin 25 mg, or placebo. Seven thousand and twenty patients were treated; 706 (10.1%) had heart failure at baseline. Heart failure hospitalization or cardiovascular death occurred in a significantly lower percentage of patients treated with empagliflozin [265/4687 patients (5.7%)] than with placebo [198/2333 patients (8.5%)] [hazard ratio, HR: 0.66 (95% confidence interval: 0.55–0.79); P , 0.001], corresponding to a number needed to treat to prevent one heart failure hospitalization or cardiovascular death of 35 over 3 years. Consistent effects of empagliflozin were observed across subgroups defined by baseline characteristics, including patients with vs. without heart failure, and across categories of medications to treat diabetes and/or heart failure. Empagliflozin improved other heart failure outcomes, including hospitalization for or death from heart failure [2.8 vs. 4.5%; HR: 0.61 (0.47–0.79); P , 0.001] and was associated with a reduction in all-cause hospitalization [36.8 vs. 39.6%; HR: 0.89 (0.82–0.96); P ¼ 0.003]. Serious adverse events and adverse events leading to discontinuation were reported by a higher proportion of patients with vs. without heart failure at baseline in both treatment groups, but were no more common with empagliflozin than with placebo.

Conclusion

In patients with type 2 diabetes and high cardiovascular risk, empagliflozin reduced heart failure hospitalization and cardiovascular death, with a consistent benefit in patients with and without baseline heart failure.

Link: https://eurheartj.oxfordjournals.org/content/ehj/early/2016/01/26/eurheartj.ehv728.full.pdf

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