Evaluation of Loop Diuretic Dosing Following Sodium-Glucose Cotransporter 2 Inhibitor Initiation in Patients With

Brooke M Trudeau1, Larry A Allen2, Sarah J Billups3

  • 1Denver Health and Hospital Authority, Denver, CO, USA.

Insights

Most heart failure patients on loop diuretics did not require dose changes after starting sodium-glucose cotransporter 2 inhibitors (SGLT2is). Dose reductions, when they occurred, typically happened within six months of SGLT2i initiation.

Area of Science:

  • Cardiology
  • Pharmacology

Background:

  • Sodium-glucose cotransporter 2 inhibitors (SGLT2is) show cardiovascular benefits in heart failure patients.
  • Many heart failure patients use loop diuretics concurrently with SGLT2is.
  • Evidence-based guidelines for adjusting loop diuretic doses with SGLT2i initiation are lacking.

Purpose of the Study:

  • To determine the frequency and magnitude of loop diuretic dose adjustments post-SGLT2i initiation in heart failure patients.
  • To analyze loop diuretic dose changes at initiation, 6 months, and 1 year after SGLT2i therapy.
  • To examine de-escalation of hypotensive medications alongside loop diuretic adjustments.

Main Methods:

  • Retrospective analysis of heart failure patients prescribed loop diuretics before SGLT2i initiation.
  • Descriptive statistics used to evaluate loop diuretic dose changes.
  • Assessment of medication changes at specific time points: initiation, 6 months, and 1 year.

Main Results:

  • 100 patients were included in the study.
  • Only 2.0% of patients had empirical loop diuretic dose reduction at SGLT2i initiation.
  • Loop diuretic dose reduction occurred in 8.0% within 6 months and 14.0% within 1 year of SGLT2i initiation.

Conclusions:

  • The majority of heart failure patients did not require loop diuretic dose modification after starting SGLT2is.
  • When loop diuretic dose reduction occurred, it was most common within six months post-SGLT2i initiation, not empirically at the start.

Related Concept Videos

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...
476
Renal Failure: Dose Adjustments01:11

Renal Failure: Dose Adjustments

In patients with renal impairment, drugs undergo significant changes in their pharmacokinetics, which require dosage adjustments to ensure safe and effective therapy.
Reduced renal clearance and elimination rate are common outcomes of renal impairment. These alterations lead to a prolonged elimination half-life and an altered apparent volume of distribution for drugs. As a result, dosage adjustments are typically necessary to maintain optimal drug levels in the body.
However, dosage adjustments...
148
Heart Failure V: Medical Management01:30

Heart Failure V: Medical Management

Medical Management of Acute Decompensated Heart Failure (ADHF)The primary goals of therapy for patients hospitalized with acute decompensated heart failure (ADHF) include:Relieving symptomsOptimizing volume statusSupporting oxygenation and ventilationMaintaining cardiac output (CO) and end-organ perfusionIdentifying and addressing the cause of ADHFPreventing complicationsProviding patient education on factors precipitating HF exacerbationPlanning for dischargeOngoing monitoring and assessment...
23
Antihypertensive Drugs: Potassium-Sparing Diuretics01:28

Antihypertensive Drugs: Potassium-Sparing Diuretics

Liddle syndrome is a genetically inherited form of hypertension characterized by the overactivity of epithelial sodium channels in the nephron, the functional unit of the kidney. This heightened activity leads to increased sodium reabsorption and excessive excretion of potassium. To counteract this, potassium-sparing diuretics such as amiloride are used. They function by blocking these sodium channels, thereby reducing the influx of sodium into the epithelial cells and minimizing the loss of...
732
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...
501
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...
708