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Researchers tracked outcomes for a median of just under 18 months. All secondary endpoints related specifically to heart failure outcomes were significantly reduced among patients who received empagliflozin. The study’s primary composite endpoint occurred in 8.2% of those who received empagliflozin and 9.1% of the control group.
Researchers tracked outcomes for a median of just under 18 months. All secondary endpoints related specifically to heart failure outcomes were significantly reduced among patients who received empagliflozin. The study’s primary composite endpoint occurred in 8.2% of those who received empagliflozin and 9.1% of the control group.
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