Abstract | OBJECTIVES: BACKGROUND: MRAs are greatly underused in patients with HFrEF, often because of fear of adverse events. Concern about hypotension has been raised by the demonstration that MRAs are particularly effective treatment for resistant hypertension. METHODS: The effect of MRA therapy was studied in 4,396 patients with HFrEF randomized in the RALES (Randomized Aldactone Evaluation Study) and EMPHASIS-HF ( Eplerenone in Mild Patients Hospitalization and Survival Study in Heart Failure) trials. RESULTS: Mean SBP change from baseline to 6 months was +1.4 ± 18.1 mm Hg in the placebo group and -1.2 ± 17.9 mm Hg in the MRA group. The between-treatment difference was 2.6 mm Hg (95% confidence interval [CI]: 1.5 to 3.6; p < 0.001). All outcomes were reduced by MRA therapy overall, with consistent effects across SBP categories (e.g., all-cause mortality, overall hazard ratio [HR] of 0.72; 95% CI: 0.64 to 0.82; p < 0.001; SBP ≤105 mm Hg; HR: 0.72; 95% CI: 0.56 to 0.94; SBP >105 to ≤115 mm Hg; HR: 0.78; 95% CI: 0.60 to 1.02; SBP >115 to ≤125 mm Hg; HR: 0.71; 95% CI: 0.53 to 0.94; SBP >125 to ≤135 mm Hg; HR: 0.79; 95% CI: 0.57 to 1.10; and SBP > 135 mm Hg; HR: 0.67; 95% CI: 0.50 to 0.90; p for interaction = 0.95). Hypotension was infrequent and not more common with MRA therapy than with placebo, overall (4.6% vs. 3.9%; p = 0.25) or in any SBP category. CONCLUSIONS: MRA treatment had little effect on SBP in patients with HFrEF, and the clinical benefits were not modified by baseline SBP. MRA treatment infrequently caused hypotension, even when the baseline SBP was low. The treatment discontinuation rates between MRA and placebo therapy were similar. Low SBP is not a reason to withhold MRA therapy in patients with HFrEF.
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Authors | Matteo Serenelli, Alice Jackson, Pooja Dewan, Pardeep S Jhund, Mark C Petrie, Patrick Rossignol, Gianluca Campo, Bertram Pitt, Faiez Zannad, João Pedro Ferreira, John J V McMurray |
Journal | JACC. Heart failure
(JACC Heart Fail)
Vol. 8
Issue 3
Pg. 188-198
(03 2020)
ISSN: 2213-1787 [Electronic] United States |
PMID | 31926854
(Publication Type: Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2020 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Mineralocorticoid Receptor Antagonists
- Spironolactone
- Eplerenone
|
Topics |
- Aged
- Blood Pressure
(drug effects, physiology)
- Eplerenone
(therapeutic use)
- Female
- Heart Failure
(drug therapy, physiopathology)
- Humans
- Male
- Mineralocorticoid Receptor Antagonists
(therapeutic use)
- Spironolactone
(therapeutic use)
- Stroke Volume
(drug effects, physiology)
- Treatment Outcome
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