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Editorial
. 2024 Aug;12(8):1487-1493.
doi: 10.1016/j.jchf.2024.03.022. Epub 2024 Jun 5.

Novel Initiative Increasing GDMT Use Among Patients With Heart Failure With Reduced Ejection Fraction

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Free article
Editorial

Novel Initiative Increasing GDMT Use Among Patients With Heart Failure With Reduced Ejection Fraction

Andrei Minciunescu et al. JACC Heart Fail. 2024 Aug.
Free article

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.

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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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