When and How to Use Sodium-Glucose Cotransporter 2 Inhibitors in Patients With Heart Failure With Reduced Ejection

Eileen O'Meara1, Subodh Verma2

  • 1Department of Cardiology, Montréal Heart Institute, Université de Montréal, Montréal, Québec, Canada.

Insights

Sodium-glucose cotransporter 2 (SGLT2) inhibitors significantly reduce heart failure hospitalizations and cardiovascular mortality in patients with heart failure with reduced ejection fraction (HFrEF). These drugs offer a favorable safety profile, even in patients with chronic kidney disease.

Area of Science:

  • Cardiology
  • Endocrinology
  • Nephrology

Background:

  • Sodium-glucose cotransporter 2 (SGLT2) inhibitors are recommended for type 2 diabetes (T2DM) and have shown benefits in heart failure (HF).
  • Recent trials like DAPA-HF and EMPEROR-Reduced confirm SGLT2 inhibitors' efficacy in heart failure with reduced ejection fraction (HFrEF).
  • These benefits extend to patients with or without T2DM and do not interact with existing HF therapies.

Purpose of the Study:

  • To summarize evidence on SGLT2 inhibitors for HFrEF.
  • To provide a practical guide for prescribing SGLT2 inhibitors in HFrEF patients.
  • To discuss the safety and efficacy of SGLT2 inhibitors in HFrEF, including those with chronic kidney disease (CKD).

Main Methods:

  • Review of major clinical trials (DAPA-HF, EMPEROR-Reduced, DAPA-CKD).
  • Analysis of outcome benefits on HF hospitalizations and cardiovascular mortality.
  • Assessment of safety profile and adverse events.

Main Results:

  • SGLT2 inhibitors significantly reduce HF hospitalizations and cardiovascular mortality in HFrEF.
  • Benefits are consistent across patients with and without T2DM.
  • Favorable safety profile observed, with no increased adverse events of concern.
  • Dapagliflozin shows renal and cardiovascular benefits in CKD patients, irrespective of diabetes status.

Conclusions:

  • SGLT2 inhibitors are crucial for managing HFrEF, offering significant outcome improvements.
  • The favorable safety profile supports their use in a broad HFrEF population, including those with CKD.
  • Understanding proposed mechanisms of action may further optimize SGLT2 inhibitor therapy in cardiovascular and renal disease.

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