Novel Initiative Increasing GDMT Use Among Patients With Heart Failure With Reduced Ejection Fraction
- PMID: 38934962
- DOI: 10.1016/j.jchf.2024.03.022
Novel Initiative Increasing GDMT Use Among Patients With Heart Failure With Reduced Ejection Fraction
Abstract
Guideline-directed medical therapy utilization in patients with heart failure with reduced ejection fraction (HFrEF) remains low despite benefits in morbidity and mortality. The authors describe a unique quality improvement initiative designed to increase angiotensin receptor-neprilysin inhibitor (ARNI) and mineralocorticoid receptor antagonist (MRA) utilization in outpatients with HFrEF in a large cardiology practice, whereby eligible patients were identified in a standardized review process and medication utilization rates were linked to group quality metrics. Eligible HFrEF patients were defined as having a left ventricular ejection fraction (LVEF) ≤40% and NYHA functional class II to IV level of symptoms. Those with an LVEF >40%, no documented LVEF, or with NYHA functional class I symptoms were excluded. ARNI utilization was defined as any dose of sacubitril/valsartan prescribed, and MRA utilization was defined as any dose of either spironolactone or eplerenone prescribed. Group quality metric targets were set at >25% ARNI prescription and >60% MRA prescription in eligible patients. Following project implementation, ARNI utilization rose from 31% to 67% and MRA increased from 28% to 66%. Establishing clear quality metrics and formulating a proactive evaluation process was associated with a significant increase in prescription rates.
Keywords: angiotensin-neprilysin inhibitor; guideline-directed medical therapy; heart failure with reduced ejection fraction; mineralocorticoid-receptor antagonist.
Copyright © 2024 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Funding Support and Author Disclosures The statistical analysis for this manuscript was supported by grant funding from iTHRIV: National Center for Advancing Translational Sciences of the National Institutes of Health under Award Number UL1TR003015/KL2TR003016. Dr O’Connor served as a consultant for Abiomed and ZealCare; and has received research funding from Merck. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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