Baroreflex activation therapy with the Barostim™ device in patients with heart failure with reduced ejection fraction: a patient level meta-analysis of randomized controlled trials.


Journal

European journal of heart failure
ISSN: 1879-0844
Titre abrégé: Eur J Heart Fail
Pays: England
ID NLM: 100887595

Informations de publication

Date de publication:
09 2022
Historique:
revised: 04 06 2022
received: 07 02 2022
accepted: 06 06 2022
pubmed: 18 6 2022
medline: 12 10 2022
entrez: 17 6 2022
Statut: ppublish

Résumé

Heart failure with reduced ejection fraction (HFrEF) remains associated with high morbidity and mortality, poor quality of life (QoL) and significant exercise limitation. Sympatho-vagal imbalance has been shown to predict adverse prognosis and symptoms in HFrEF, yet it has not been specifically targeted by any guideline-recommended device therapy to date. Barostim™, which directly addresses this imbalance, is the first Food and Drug Administration approved neuromodulation technology for HFrEF. We aimed to analyse all randomized trial evidence to evaluate the effect of baroreflex activation therapy (BAT) on heart failure symptoms, QoL and N-terminal pro-brain natriuretic peptide (NT-proBNP) in HFrEF. An individual patient data (IPD) meta-analysis was performed on all eligible trials that randomized HFrEF patients to BAT + guideline-directed medical therapy (GDMT) or GDMT alone (open label). Endpoints included 6-month changes in 6-min hall walk (6MHW) distance, Minnesota Living With Heart Failure (MLWHF) QoL score, NT-proBNP, and New York Heart Association (NYHA) class in all patients and three subgroups. A total of 554 randomized patients were included. In all patients, BAT provided significant improvement in 6MHW distance of 49 m (95% confidence interval [CI] 33, 64), MLWHF QoL of -13 points (95% CI -17, -10), and 3.4 higher odds of improving at least one NYHA class (95% CI 2.3, 4.9) when comparing from baseline to 6 months. These improvements were similar, or better, in patients who had baseline NT-proBNP <1600 pg/ml, regardless of the cardiac resynchronization therapy indication status. An IPD meta-analysis suggests that BAT improves exercise capacity, NYHA class, and QoL in HFrEF patients receiving GDMT. These clinically meaningful improvements were consistent across the range of patients studies. BAT was also associated with an improvement in NT-proBNP in subjects with a lower baseline NT-proBNP.

Identifiants

pubmed: 35713888
doi: 10.1002/ejhf.2573
pmc: PMC9796660
doi:

Substances chimiques

Peptide Fragments 0
Natriuretic Peptide, Brain 114471-18-0

Types de publication

Journal Article Meta-Analysis Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1665-1673

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL151744
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

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Auteurs

Andrew J S Coats (AJS)

University of Warwick, Coventry, UK.

William T Abraham (WT)

Division of Cardiovascular Medicine, The Ohio State University, Columbus, OH, USA.

Michael R Zile (MR)

The Medical University of South Carolina and the RHJ Department of Veterans Affairs Medical Center, Charleston, SC, USA.

Joann A Lindenfeld (JA)

Vanderbilt Heart and Vascular Institute, Nashville, TN, USA.

Fred A Weaver (FA)

Division of Vascular Surgery and Endovascular Therapy, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.

Marat Fudim (M)

Duke University Medical Center, Durham, NC, USA.
Duke Clinical Research Institute, Durham, NC, USA.

Johann Bauersachs (J)

Department of Cardiology and Angiology, Hannover Medical School, Hannover, Germany.

Sue Duval (S)

Cardiovascular Division, University of Minnesota Medical School, Minneapolis, MN, USA.

Elizabeth Galle (E)

CVRx®, Inc., Minneapolis, MN, USA.

Faiez Zannad (F)

Université de Lorraine, Inserm Centre d'Investigation, CHU, Université de Lorraine, Nancy, France.

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