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Predictors of the Use of Mineralocorticoid Receptor Antagonists in Patients With Left Ventricular Dysfunction
Eric C Wong1, Christopher B Fordyce2,3,4, Graham Wong2,4
1Division of General Internal Medicine Department of Medicine University of British Columbia Vancouver British Columbia Canada.
Insights
Mineralocorticoid receptor antagonists (MRAs) are recommended for eligible heart attack patients, but real-world use remains low. Only 22% received MRAs at discharge, highlighting a gap in post-heart attack care and the need for better decision support.
Area of Science:
- Cardiology
- Pharmacotherapy
- Outcomes Research
Background:
- Mineralocorticoid receptor antagonists (MRAs) are guideline-recommended post-myocardial infarction (MI) for patients with heart failure or diabetes mellitus.
- Efficacy and survival benefits are established in trials like EPHESUS, particularly for those with reduced left ventricular ejection fraction (LVEF).
Purpose of the Study:
- To assess the real-world utilization of MRAs in patients who experienced ST-segment-elevation myocardial infarction (STEMI) and developed left ventricular dysfunction.
- To identify factors influencing MRA prescription rates in this high-risk population.
Main Methods:
- A prospective, population-based study linked STEMI registry data with cardiology outpatient records (2007-2018).
- Eligibility for MRAs was defined using EPHESUS criteria: LVEF ≤40% plus clinical heart failure or diabetes mellitus, excluding dialysis-dependent renal dysfunction.
- Primary outcome: MRA prescription at discharge; Secondary outcome: MRA prescription within 3 months post-discharge.
Main Results:
- Of 2691 STEMI patients, 317 (12%) met MRA eligibility criteria.
- Only 70 (22%) eligible patients received an MRA at discharge.
- Among those not prescribed an MRA at discharge, 9.5% received one within 3 months.
- Lower LVEF and later calendar year were associated with increased MRA prescription at discharge.
Conclusions:
- Real-world MRA uptake in eligible STEMI patients remains suboptimal, with only about one-quarter prescribed within 3 months post-hospitalization.
- Significant gaps exist in guideline-directed medical therapy for post-STEMI care.
- Development of decision-support tools is crucial to improve MRA prescribing and address this care gap.
Abstract:
Background Guidelines recommend mineralocorticoid receptor antagonist (MRA) use in patients with left ventricular ejection fraction ≤40% following a myocardial infarction plus heart failure or diabetes mellitus, based on mortality benefit in the EPHESUS (Eplerenone Post-Acute Myocardial Infarction Heart Failure Efficacy and Survival Study) trial. The objective of this study was to evaluate the real-world utilization of MRAs for patients with ST-segment-elevation myocardial infarction (STEMI) with left ventricular dysfunction. Methods and Results The prospective, population-based, Vancouver Coastal Health Authority STEMI database was linked with local outpatient cardiology records from 2007 to 2018. EPHESUS criteria were used to define post-STEMI MRA eligibility (left ventricular ejection fraction ≤40% plus clinical heart failure or diabetes mellitus, and no dialysis-dependent renal dysfunction). The primary outcome was MRA prescription among eligible patients at discharge and the secondary outcome was MRA prescription within 3 months postdischarge. Of 2691 patients with STEMI, 317 (12%) were MRA eligible, and 70 (22%) eligible patients were prescribed an MRA at discharge. Among eligible patients with no MRA at discharge, 12/126 (9.5%) with documented postdischarge follow-up were prescribed an MRA within 3 months. In multivariable analysis, left ventricular ejection fraction (odds ratio [OR], 1.55 per 5% left ventricular ejection fraction decrease; 95% CI, 1.26-1.90) and calendar year (OR, 1.23 per year, 95% CI, 1.11-1.37) were associated with MRA prescription at discharge. Other prespecified variables were not associated with MRA prescription. Conclusions In this contemporary STEMI cohort, only 1 in 4 MRA-eligible patients were prescribed an MRA within 3 months following hospitalization despite high-quality evidence for use. Novel decision-support tools are required to optimize pharmacotherapy decisions during hospitalization and follow-up to target this gap in post-STEMI care.
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