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Current Vascular Pharmacology

Editor-in-Chief

ISSN (Print): 1570-1611
ISSN (Online): 1875-6212

Review Article

Effect of Mineralocorticoid Receptor Antagonists in Heart Failure with Preserved Ejection Fraction and with Reduced Ejection Fraction - A Narrative Review

Author(s): Adriana Mares, Tayana Rodriguez, Abhizith Deoker, Angelica Lehker and Debabrata Mukherjee*

Volume 20, Issue 1, 2022

Published on: 20 July, 2021

Page: [46 - 51] Pages: 6

DOI: 10.2174/1570161119666210720120439

Price: $65

Abstract

Background: Heart failure is a major cause of morbidity and mortality globally. By the end of this decade, ~8 million Americans will have heart failure with an expenditure of $69.8 billion.

Objective: In this narrative review, we evaluate the benefits, potential risks and the role of Mineralocorticoid Receptor Antagonists (MRAs) in the management of both Heart Failure with Preserved Ejection Fraction (HFpEF) and Heart Failure with Reduced Ejection Fraction (HFrEF).

Methods: We performed a comprehensive literature review to assess the available evidence on the role of MRAs in heart failure using the online databases (PubMed, Embase, Scopus, CINAHL and Google Scholar).

Results: Clinical evidence shows that MRAs such as spironolactone and eplerenone reduce mortality and readmissions for patients with HFrEF compared with placebo. Furthermore, one trial reported that MRAs reduce heart failure hospitalization in patients with HFpEF. The American College of Cardiology/American Heart Association Guidelines strongly recommend using MRA in patients with reduced Left Ventricular Ejection Fraction (LVEF) with Class II-IV symptoms, estimated glomerular filtration rate >30 ml/min/1.73 m2, and absence of hyperkalemia. Despite this, MRAs are underutilized in the management of heart failure.

Conclusions: MRAs improve outcomes in patients with both HFpEF and HFrEF but remain underutilized.

Keywords: Heart failure with preserved ejection fraction, heart failure with reduced ejection fraction, mineralocorticoid receptor antagonists, heart failure, left ventricular ejection fraction, readmission.

Graphical Abstract

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