Prescribing patterns of SGLT-2 inhibitors for patients with heart failure: A two-center analysis

Teja Chakrala1, Roshni O Prakash1, Justin Kim1

  • 1Department of Medicine, University of Florida, Gainesville, FL, United States of America.

Insights

Sodium glucose co-transporter 2 inhibitors (SGLT2i) show low prescription rates in heart failure patients despite proven benefits. This study identifies barriers to SGLT2i implementation in clinical practice.

Area of Science:

  • Cardiology
  • Pharmacology
  • Clinical Practice

Background:

  • Sodium glucose co-transporter 2 inhibitors (SGLT2i) reduce cardiovascular death and hospitalizations in heart failure (HF) patients, regardless of diabetes status.
  • Despite strong recommendations, SGLT2i prescription rates for heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction (HFpEF) remain low.

Purpose of the Study:

  • To analyze SGLT2i prescription patterns at two academic institutions.
  • To identify barriers hindering the implementation of SGLT2i in heart failure management.

Main Methods:

  • Retrospective analysis of patients (≥18 years) diagnosed with heart failure admitted between May 2021 and May 2022.
  • Inclusion criteria: eGFR ≥20 mL/min/1.73m², BNP ≥100 pg/mL.
  • Data collected on SGLT2i prescription rates and associated factors.

Main Results:

  • SGLT2i prescribed in only 1.8% of HFpEF and 3.2% of HFrEF patients.
  • Cardiologist approval was required for most HFpEF SGLT2i prescriptions from general medicine.
  • No significant association found between SGLT2i use and adverse events like hypoglycemia or UTIs.

Conclusions:

  • Implementation of SGLT2i in heart failure management is significantly low despite established efficacy.
  • Barriers to SGLT2i uptake in clinical practice require further investigation and intervention.
Abstract

Related Concept Videos

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
428
Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
584
Heart Failure Drugs: Diuretics01:22

Heart Failure Drugs: Diuretics

Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
370
Heart Failure Drugs: β-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
338
Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
184