Empagliflozin associated with reduced MACE, heart failure, and mortality versus DPP4 inhibitors in observational Medicare study
Using propensity score-matched Medicare claims data (2014-2020), this real-world analysis compared adults aged ≥65 with type 2 diabetes who initiated empagliflozin versus dipeptidyl peptidase-4 inhibitors or GLP-1 receptor agonists. Empagliflozin was associated with lower rates of major adverse cardiovascular events (HR 0.77), hospitalization for heart failure (HR 0.72), and all-cause mortality (HR 0.66) versus DPP4 inhibitors, with consistent effects across sociodemographic subgroups but greater absolute benefits in those with prevalent cardiovascular disease.
What this changes
The finding has not established an approved change to our evidence assessment.
Source date: Sep 21, 2026 · Discovered: Sep 21, 2026 · Assessed: — · Research update
What it does not prove
- Limitations have not yet been verified. Read the primary source.
Extracted from supplied source material; model confidence is not a measured probability of correctness.
Study details
- Design
- Cohort
- Sample size
- —
- Duration
- —
- Population
- Adults aged ≥65 years with type 2 diabetes from Medicare claims data (2014-2020), propensity score-matched
- Primary outcome
- Major adverse cardiovascular events (MACE), hospitalization for heart failure (HHF), and all-cause mortality (ACM)
- Effect size
- MACE: HR 0.77 (99.9% CI [0.69, 0.85]), IRD = -10.3 [-14.1, -6.4]; HHF vs DPP4is: HR 0.72 (CI [0.67, 0.79]), IRD = -18.3 [-22.9, -13.6]; ACM vs DPP4is: HR 0.66 (CI [0.57, 0.76]), IRD = -8.6 [-11.4, -5.8]; HHF vs GLP-1RAs: HR 0.88 (CI [0.81, 0.95]), IRD = -6.9 [-10.8, -3.1]
- Significance
- Significant
- Journal
- Diabetes Care
- Published
- Sep 21, 2026
Sources
Primary source
- Diabetes care ↗Peer reviewed
Assessment history
9/24/2026 · SUPERSEDED: Source updated; assessment withdrawn pending review.
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