Relative Efficacy of Spironolactone, Eplerenone, and cAnRenone in patients with Chronic Heart failure (RESEARCH): a systematic review and network meta-analysis of randomized controlled trials.


Journal

Heart failure reviews
ISSN: 1573-7322
Titre abrégé: Heart Fail Rev
Pays: United States
ID NLM: 9612481

Informations de publication

Date de publication:
03 2020
Historique:
pubmed: 1 8 2019
medline: 18 3 2021
entrez: 1 8 2019
Statut: ppublish

Résumé

This study aims to assess the comparative benefit and risk profile of treatment with mineralocorticoid receptor antagonists (MRAs) with regard to all-cause mortality (primary endpoint), cardiovascular mortality, or heart failure (HF)-related hospitalization (secondary endpoints) and the safety endpoints hyperkalemia, acute renal failure, and gynecomastia in patients with chronic HF. We conducted a systematic review and network meta-analysis following PRISMA-P and PRISMA-NMA guidelines. From 16 different sources, 14 randomized controlled trials totaling 12,213 patients testing an active treatment of either spironolactone, eplerenone, or canrenone/potassium-canreonate in adults with symptomatic HF due to systolic dysfunction reporting any of the above endpoints were retained. Efficacy in comparison to placebo/standard medical care with respect to all-cause mortality was confirmed for spironolactone and eplerenone while no conclusion could be drawn for canrenone (HR 0.69 (0.62; 0.77), 0.82 (0.75; 0.91), and 0.50 (0.17; 1.45), respectively). Indirect comparisons hint a potential (non-significant) preference of spironolactone over eplerenone (HR 0.84 (0.68; 1.03)). The overall risk of bias was low to intermediate. Results for secondary endpoints as well as sensitivity analyses essentially mirrored these findings. The beta-blocker adjusted meta-analysis for the primary endpoint showed the same tendency as the unadjusted one (HR 0.39 (0.07; 2.03)). Results need to be interpreted with caution, though, as the resultant mix of patient- and study-level covariates produced unstable statistical modeling. We found no significant and systematic superiority of either MRA regarding efficacy toward all endpoints considered in both direct and indirect comparisons.

Identifiants

pubmed: 31364027
doi: 10.1007/s10741-019-09832-y
pii: 10.1007/s10741-019-09832-y
doi:

Substances chimiques

Diuretics 0
Mineralocorticoid Receptor Antagonists 0
Spironolactone 27O7W4T232
Eplerenone 6995V82D0B
Canrenone 78O20X9J0U

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

161-171

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Auteurs

Lutz Frankenstein (L)

Department of Cardiology, Angiology and Pulmology, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany. Lutz.Frankenstein@med.uni-heidelberg.de.

Svenja Seide (S)

Institute of Medical Biometry and Informatics, University Hospital Heidelberg, Heidelberg, Germany.

Tobias Täger (T)

Department of Cardiology, Angiology and Pulmology, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.

Katrin Jensen (K)

Institute of Medical Biometry and Informatics, University Hospital Heidelberg, Heidelberg, Germany.

Hanna Fröhlich (H)

Department of Cardiology, Angiology and Pulmology, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.

Andrew L Clark (AL)

Hull York Medical School at Castle Hill Hospital, Hull, UK.

Mirjam Seiz (M)

Department of Cardiology, Angiology and Pulmology, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.

Hugo A Katus (HA)

Department of Cardiology, Angiology and Pulmology, University Hospital Heidelberg, Im Neuenheimer Feld 410, 69120, Heidelberg, Germany.

Paul Nee (P)

Marketing Group, Gamida-Cell, Cambridge, MA, USA.

Lorenz Uhlmann (L)

Institute of Medical Biometry and Informatics, University Hospital Heidelberg, Heidelberg, Germany.

Huseyin Naci (H)

Department of Health Policy, London School of Economics and Political Science, London, UK.

Dan Atar (D)

Department of Cardiology, Oslo University Hospital, Ulleval and Institute of Clinical Sciences, University of Oslo, Oslo, Norway.

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Classifications MeSH