Type 2 & other diabetes

Empagliflozin in Patients With Type 2 Diabetes Undergoing On-Pump Coronary Artery Bypass Grafting (CABG): The POST-CABGDM Randomized Clinical Trial

Diabetes CarePublished Randomised controlled trial

Primary result · Postoperative AKIResult — go to the resultRelative risk 0.57 95% CI 0.34–0.96

Authors' conclusion

Empagliflozin use before on-pump CABG in patients with T2DM was associated with a reduced incidence of postoperative AKI without an increase in safety events. These findings warrant confirmation in larger clinical trials.

Study context

Population
Patients with T2D scheduled for elective on-pump CABG, Brazilrandomized
Participants
145 patients
Comparison
Empagliflozin 25 mg daily plus standard care vs standard care alone
  • Empagliflozinn = 71
  • Standard caren = 74reference
Primary endpoint
Postoperative acute kidney injury (AKI) by creatinine-based criteria (AKIN, RIFLE or KDIGO)
Follow-up
Within 7 days of surgery
Methodological detailsinvestigator-initiated, pragmatic, single-centre, open-label, blinded outcome adjudication
  • Investigator-initiated
  • Pragmatic
  • Single-centre
  • Open-label
  • Blinded outcome adjudication

Primary result

Postoperative AKI

Relative risk

0.57

95% CI 0.34–0.96

P = 0.03

By group

Empagliflozinvs Standard care
RR 0.57 (95% CI 0.34–0.96); P = 0.03

As reported in the abstract

Secondary outcomes

30-day postoperative AF

Rates of AF similar between groups (15.4% vs. 13.5%)
RR 1.15 (95% CI 0.52-2.53); P = 0.73

30-day type 5 myocardial infarction (MI)

Rates of type 5 MI similar between groups (1.4% vs. 4.1%)
RR 0.35 (95% CI 0.04-3.26); P = 0.62

Deaths

Deaths, all in the control group
3

Safety

Safety events (ketoacidosis, UTI, hospital-acquired pneumonia, wound infection) · within 30 days after CABG

No statistically significant differences between groups for safety events

Original publication

Empagliflozin in Patients With Type 2 Diabetes Undergoing On-Pump CABG: The POST-CABGDM Randomized Clinical Trial. Diabetes Care. Published 15 April 2025. doi:10.2337/dc24-2807

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