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.

Related Concept Videos

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...
612
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...
570
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...
58
Heart Failure Drugs: β-Blockers01:22

Heart Failure Drugs: β-Blockers

β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
530
Antianginal Drugs: Calcium Channel Blockers and Ranolazine01:25

Antianginal Drugs: Calcium Channel Blockers and Ranolazine

Angina pectoris, a primary symptom of ischemic heart disease, requires careful pharmacological interventions. In this context, calcium channel blockers (CCBs) and ranolazine have emerged as crucial pharmacotherapeutic agents, providing deep insights into the complexities of angina management.
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
854
Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers01:24

Antiarrhythmic Drugs: Class II Agents as β-Adrenergic Blockers

Adrenergic stimulation generally impacts cardiac rate and rhythm. Specifically, stimulation of the β-adrenoceptors triggers an increase in intracellular calcium ion influx and pacemaker currents, which may cause arrhythmias. Catecholamines like adrenaline also demonstrate β2-adrenoceptor-mediated hypokalemia, impacting cardiac action potential and disrupting the normal cardiac rhythm. Class II antiarrhythmic drugs are β-adrenoceptor antagonists or β-blockers, which...
1.1K