In REWIND participants, dulaglutide did not significantly reduce heart failure events versus placebo.
In plain wordsDulaglutide did not significantly reduce heart failure events compared with placebo.
- Peptide
- Dulaglutide (Trulicity)
- Outcome
- No significant changeHeart failure events
- Study
n = 9,901
- Comparator
- Placebo
- Outcome group
- Heart function · Cardiovascular
- Studied dose
- Dose not stated · Median 5.4 yearsAs given in this study (human).
Measurements
- HF events
- 213 participants
- dulaglutide
- HF event proportion
- 4.3%
- dulaglutide
- HF events
- 226 participants
- placebo
- HF event proportion
- 4.6%
- placebo
- Hazard ratio
- 0.93 ratio
- dulaglutide versus placebo
- 95% CI lower
- 0.77 ratio
- HF hazard ratio
- 95% CI upper
- 1.12 ratio
- HF hazard ratio
Source sentences
Of the 9901 participants studied over a median follow-up of 5.4 years, 213/4949 (4.3%) randomly assigned to dulaglutide and 226/4952 (4.6%) participants assigned to placebo experienced a HF event (hazard ratio [HR] 0.93, 95% confidence interval [CI] 0.77-1.12; p = 0.456).
2 context sentences(design, population, supporting numbers)
We examined the effect of the glucagon-like peptide 1 agonist dulaglutide on incident HF events and other cardiovascular outcomes in those with or without prior HF in the randomized placebo-controlled Researching Cardiovascular Events with a Weekly Incretin in Diabetes (REWIND) trial.
In this post-hoc analysis, a HF event was defined as an adjudication-confirmed hospitalization or urgent evaluation for HF.