Aldosterone antagonists improve ejection fraction and functional capacity independently of functional class: a meta-analysis of randomised controlled trials

Heart. 2012 Dec;98(23):1693-700. doi: 10.1136/heartjnl-2012-302178. Epub 2012 Jul 12.

Abstract

Context: Current guidelines recommend the use of aldosterone antagonists (AA) in patients with moderately severe to severe symptoms [New York Heart Association (NYHA) class III to IV] and systolic heart failure.

Objective: To determine the efficacy of AA in improving ejection fraction (EF) and functional capacity and to assess whether this effect was influenced by baseline NYHA classification.

Study design: Meta-analysis of randomized controlled trials. Data extraction performed independently by two researchers.

Data sources: MEDLINE and the Cochrane Library.

Study selection: Prospective randomized controlled trials using AA were included if there was a clear description of the baseline NYHA classification and change in EF in patients from study initiation to completion.

Results: Data from 1,575 patients enrolled in fourteen studies were included. Overall, there was a weighted mean improvement in EF of 3.2% and in NYHA classification of 0.13 in subjects treated with AA when compared to controls (p<0.001). A mixed effects meta-regression analysis revealed that baseline NYHA was not predictive of improvement in EF (p=0.67) nor NYHA status (p=0.18).

Conclusions: The results of this meta-analysis suggest that AA is associated with significant improvements in EF and functional class independent of baseline functional capacity. This supports and expands on the recently published EMPHASIS-HF trial and suggests that the current restriction of AA use to patients with NYHA class III-IV symptoms should be reconsidered.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Heart Failure / drug therapy*
  • Heart Failure / physiopathology
  • Humans
  • Mineralocorticoid Receptor Antagonists / therapeutic use*
  • Randomized Controlled Trials as Topic*
  • Stroke Volume / drug effects
  • Stroke Volume / physiology*
  • Treatment Outcome
  • Ventricular Function / drug effects*
  • Ventricular Function / physiology

Substances

  • Mineralocorticoid Receptor Antagonists