Congestive heart failure Sodium-glucose co-transporter 2 inhibitors

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Editor(s)-In-Chief: C. Michael Gibson, M.S., M.D.; Associate Editor(s)-In-Chief: Mitra Chitsazan, M.D.[1]

Overview

Sodium-glucose co-transporter 2 (SGLT2) inhibitors (dapagliflozin or empagliflozin) are recommended for patients with HFrEF regardless of the presence or absence of diabetes, in addition to optimal medical therapy with an ACE-I/ARNI, a beta-blocker, and an aldosterone antagonist.

Sodium-glucose co-transporter 2 inhibitors

Indications for Sodium-glucose co-transporter 2 inhibitors

According to the 2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure, all patients should be on a Sodium-glucose co-transporter 2 inhibitors if: [1]

1. The left ventricular ejection fraction (LVEF) is ≤ 40%

AND

2. The patient is already taking an ACE-I/ARNI, a beta-blocker, and an aldosterone antagonist.

  • SGLT2 inhibitors should be administered for all patients with HFrEF regardless of diabetes status.

Background

  • In DAPA-HF trial- a phase 3, placebo-controlled trial- 4744 patients with NYHA class II–IV, and an LVEF ≤40% despite optimal medical therapy (OMT) were randomly assigned to receive dapagliflozin (10 mg once daily) or placebo, in addition to OMT [2]. The primary outcome was a composite of worsening HF (hospitalization or an urgent visit resulting in i.v. therapy for HF) or cardiovascular (CV) death. Results showed that over a median of 18.2 months, dapagliflozin resulted in a 26% reduction in the primary endpoint. Similar benefits were seen in patients with and without diabetes.
  • In the EMPEROR-Reduced trial, 3730 patients with NYHA class II–IV, and an LVEF ≤40% despite optimal medical therapy (OMT) were randomly assigned to receive empagliflozin (10 mg once daily) or placebo, in addition to OMT [3]. The primary outcome was a composite of CV death or hospitalization for worsening HF. Results showed that over a median of 16 months empagliflozin reduced the primary endpoint by 25%.
  • Therefore, dapagliflozin or empagliflozin are recommended for patients with HFrEF regardless of the presence or absence of diabetes, in addition to optimal medical therapy with an ACE-I/ARNI, a beta-blocker, and an MRA [1]

. SGLT2 inhibitors also have diuretic/natriuretic effects which may provide additional benefits in reducing volume overload and congestion and thus may allow a reduction in the need to loop diuretics.

Dosing

SGLT2 inhibitor [1] Starting dose Target dose
Dapagliflozin 10 mg QD 10 mg QD
Empagliflozin 10 mg QD 10 mg QD

Adverse effect

  • The most common side effects of SGLT2 inhibitors results from glucosuria and include: [3]
  • Genital fungal infections (e.g. vaginal candidiasis)
  • Urinary tract infection
  • Osmotic diuresis–related adverse events, such as volume depletion and a small reduction in eGFR following initiation.
    • However, this effect is transient and reversible, and premature discontinuation of the drug is not needed.
  1. 1.0 1.1 1.2 McDonagh TA, Metra M, Adamo M, Gardner RS, Baumbach A, Böhm M; et al. (2021). "2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure". Eur Heart J. 42 (36): 3599–3726. doi:10.1093/eurheartj/ehab368. PMID 34447992 Check |pmid= value (help).
  2. McMurray JJV, Solomon SD, Inzucchi SE, Køber L, Kosiborod MN, Martinez FA; et al. (2019). "Dapagliflozin in Patients with Heart Failure and Reduced Ejection Fraction". N Engl J Med. 381 (21): 1995–2008. doi:10.1056/NEJMoa1911303. PMID 31535829. Review in: Ann Intern Med. 2020 Feb 18;172(4):JC16
  3. 3.0 3.1 Packer M, Anker SD, Butler J, Filippatos G, Pocock SJ, Carson P; et al. (2020). "Cardiovascular and Renal Outcomes with Empagliflozin in Heart Failure". N Engl J Med. 383 (15): 1413–1424. doi:10.1056/NEJMoa2022190. PMID 32865377 Check |pmid= value (help). Review in: Ann Intern Med. 2020 Nov 17;173(10):JC51