SGLT2 Inhibitors and AKI Risk in Hospitalized Patients: A Reassessment
New data from a 42,000-patient retrospective cohort challenges prior concerns about perioperative SGLT2 inhibitor use
Dr. Priya Mehta
Associate Professor, Division of Nephrology, Johns Hopkins
◆ CLINICAL BOTTOM LINE
What was studied
Whether SGLT2 inhibitor use in the 30 days prior to hospitalization is independently associated with AKI in a large real-world cohort of 42,318 patients.
What was found
SGLT2 inhibitor use was associated with a 23% reduction in AKI risk (adjusted OR 0.77, 95% CI 0.68–0.87) after controlling for baseline eGFR, diabetes severity, and comorbidities.
What it changes in practice
These data support reconsidering blanket "hold SGLT2i" policies perioperatively, particularly in patients with CKD and preserved eGFR. A risk-stratified approach is warranted.
The perioperative management of SGLT2 inhibitors has been a source of ongoing debate since the emergence of euglycemic DKA as a recognized complication. Current guidelines from the American Diabetes Association recommend holding SGLT2 inhibitors 3–4 days before elective surgery, a recommendation that has been broadly extrapolated to all hospitalizations.
However, a new retrospective cohort study published in the *Journal of the American Society of Nephrology* challenges the assumption that SGLT2 inhibitor use increases AKI risk in hospitalized patients.
Study Design
Investigators analyzed 42,318 patients hospitalized at 14 academic medical centers between 2022 and 2025. Patients were stratified by SGLT2 inhibitor use in the 30 days prior to admission. The primary outcome was AKI stage 1 or higher by KDIGO criteria within 72 hours of admission.
Key Findings
After multivariable adjustment, SGLT2 inhibitor use was associated with a 23% reduction in AKI risk (adjusted OR 0.77, 95% CI 0.68–0.87, p<0.001). This protective association was most pronounced in patients with baseline eGFR 30–60 mL/min/1.73m² and in those admitted for cardiac or infectious indications.
The proposed mechanism involves SGLT2 inhibitor-mediated reduction in tubuloglomerular feedback, leading to afferent arteriolar dilation and improved medullary oxygenation under conditions of hemodynamic stress.
Limitations
As a retrospective study, residual confounding cannot be excluded. Patients who continued SGLT2 inhibitors may represent a healthier, more closely monitored population. Prospective randomized data are needed before practice change can be definitively recommended.
Clinical Implications
These findings add to a growing body of evidence suggesting that the renoprotective effects of SGLT2 inhibitors may extend to the acute setting. Nephrologists should be involved in perioperative medication reconciliation decisions, particularly for patients with CKD where the risk-benefit calculation is most nuanced.
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CME Assessment
According to the featured study, SGLT2 inhibitor use was associated with what change in AKI risk?