In propensity-matched adults with type 2 diabetes, semaglutide and empagliflozin did not differ significantly in the composite of death, MI or stroke (HR 0.89; 95% CI 0.78 to 1.02).
In plain wordsIn adults with type 2 diabetes, semaglutide users and empagliflozin users did not differ clearly in death, heart attack or stroke combined.
- Peptide
- Semaglutide
- Outcome
- No significant changeComposite of death, myocardial infarction or stroke
- Study
n = 15,798
- Comparator
- Empagliflozin
- Analysis
- Primary
- Outcome group
- Cardiovascular events · Cardiovascular
- Studied dose
- Dose not stated
Measurements
- Hazard ratio
- 0.89 HR
- semaglutide versus empagliflozin
Source sentences
Corresponding incidence rates for the composite outcome were 20.99 versus 23.56 per 1000 person-years, with a hazard ratio (HR) of 0.89 (95% CI, 0.78 to 1.02).
3 context sentences(design, population, supporting numbers)
the respective rates of the composite of death, MI, or stroke were 3.7% versus 4.5% at 2 years and 5.9% versus 6.9% at 3 years.
Target trial emulation studies from observational data comparing semaglutide- or dulaglutide-treated patients with propensity score-matched patients treated with empagliflozin.
Patients aged 45 years or older with type 2 diabetes treated from 1 January 2019 to 31 December 2024 with semaglutide, dulaglutide, or empagliflozin.