» Articles » PMID: 26720043

Renin-angiotensin-aldosterone System Blockers for Heart Failure with Reduced Ejection Fraction or Left Ventricular Dysfunction: Network Meta-analysis

Overview
Journal Int J Cardiol
Publisher Elsevier
Date 2016 Jan 1
PMID 26720043
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Renin-angiotensin-aldosterone system (RAAS) blockers are effective therapies for heart failure and reduced ejection fraction (HFrEF) or left ventricular dysfunction (LVD). We aimed to assess the efficacy and safety of RAAS blockers in these patients.

Methods: We searched MEDLINE, EMBASE, and Cochrane Library in May 2015. Twenty-one double-blind randomized controlled trials (RCTs) with 69,229 patients were included this network meta-analysis.

Results: Compared with placebo, an angiotensin receptor-neprilysin inhibitor (ARNI) had the highest probability of reducing all-cause mortality (odds ratio [OR]=0.67, 95% credible interval [CrI]: 0.48-0.86), followed by an aldosterone receptor antagonist (ARA, OR=0.74, 95% CrI: 0.62-0.88) and an angiotensin-converting enzyme inhibitor (ACEI, OR=0.80, 95% CrI: 0.71-0.89). The most efficacious therapy for preventing heart failure hospitalization was ARNI (OR=0.55, 95% CrI: 0.40-0.71), followed by combination therapy with an angiotensin II receptor blocker (ARB) plus an ACEI (OR=0.61, 95% CrI: 0.49-0.75), then an ACEI alone (OR=0.69, 95% CrI: 0.61-0.77). Sensitivity analysis restricted to nine RCTs with a high background use of ACEI and/or ARB (>80%) indicated that adding an ARA to current standard therapy significantly reduced mortality (OR=0.73, 95% CrI: 0.51-0.95) and hospitalization risk (OR=0.67, 95% CrI: 0.47-0.87), but did not significantly increase the discontinuation risk (OR=1.29, 95% CrI: 0.83-2.31).

Conclusions: ARNI has the highest probability of being the most efficacious therapy for HFrEF in reducing death and hospitalization for heart failure. ARA has the most favorable benefit-risk profile as an adjunct to background ACEI and/or ARB therapy.

Citing Articles

Novel Biomarkers as Potential Predictors of Decompensated Advanced Chronic Heart Failure-Single Center Study.

Frohling T, Semo D, Mirna M, Paar V, Shomanova Z, Motloch L J Clin Med. 2024; 13(22).

PMID: 39598008 PMC: 11594948. DOI: 10.3390/jcm13226866.


The contemporary role of sodium-glucose co-transporter 2 inhibitor (SGLT2i) and angiotensin receptor-neprilysin inhibitor (ARNI) in the management of heart failure: State-of-the-art review.

Ezhumalai B, Modi R, Panchanatham M, Kaliyamoorthy D Indian Heart J. 2024; 76(4):229-239.

PMID: 39009078 PMC: 11451353. DOI: 10.1016/j.ihj.2024.07.005.


Comparative cardiovascular outcomes of novel drugs as an addition to conventional triple therapy for heart failure with reduced ejection fraction (HFrEF): a network meta-analysis of randomised controlled trials.

Suebsaicharoen T, Chunekamrai P, Yingchoncharoen T, Tansawet A, Issarawattana T, Numthavaj P Open Heart. 2023; 10(2).

PMID: 37940331 PMC: 10632908. DOI: 10.1136/openhrt-2023-002364.


Effects of Renin-Angiotensin-Aldosterone System Inhibition on Left Ventricular Hypertrophy, Diastolic Function, and Functional Status in Patients With Hypertrophic Cardiomyopathy: A Systematic Review.

Akhtar H, Sudani H, Hussein M, Farhan M, Elkholy K Cureus. 2022; 14(7):e26642.

PMID: 35949750 PMC: 9356743. DOI: 10.7759/cureus.26642.


The prognosis and therapeutic management of patients hospitalized for heart failure in 2010-2020.

Mayer O, Bruthans J, Bilkova S, Seidlerova J, Jirak J, Filipovsky J Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2022; 166(3):312-321.

PMID: 35444330 DOI: 10.5507/bp.2022.020.