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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
AIMS: 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 specificall...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796660/ https://www.ncbi.nlm.nih.gov/pubmed/35713888 http://dx.doi.org/10.1002/ejhf.2573 |
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author | Coats, Andrew J.S. Abraham, William T. Zile, Michael R. Lindenfeld, Joann A. Weaver, Fred A. Fudim, Marat Bauersachs, Johann Duval, Sue Galle, Elizabeth Zannad, Faiez |
author_facet | Coats, Andrew J.S. Abraham, William T. Zile, Michael R. Lindenfeld, Joann A. Weaver, Fred A. Fudim, Marat Bauersachs, Johann Duval, Sue Galle, Elizabeth Zannad, Faiez |
author_sort | Coats, Andrew J.S. |
collection | PubMed |
description | AIMS: 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. METHODS AND RESULTS: 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. CONCLUSION: 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. |
format | Online Article Text |
id | pubmed-9796660 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97966602023-01-04 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 Coats, Andrew J.S. Abraham, William T. Zile, Michael R. Lindenfeld, Joann A. Weaver, Fred A. Fudim, Marat Bauersachs, Johann Duval, Sue Galle, Elizabeth Zannad, Faiez Eur J Heart Fail Devices AIMS: 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. METHODS AND RESULTS: 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. CONCLUSION: 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. John Wiley & Sons, Ltd. 2022-07-03 2022-09 /pmc/articles/PMC9796660/ /pubmed/35713888 http://dx.doi.org/10.1002/ejhf.2573 Text en © 2022 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Devices Coats, Andrew J.S. Abraham, William T. Zile, Michael R. Lindenfeld, Joann A. Weaver, Fred A. Fudim, Marat Bauersachs, Johann Duval, Sue Galle, Elizabeth Zannad, Faiez 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 |
title | 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 |
title_full | 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 |
title_fullStr | 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 |
title_full_unstemmed | 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 |
title_short | 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 |
title_sort | 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 |
topic | Devices |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9796660/ https://www.ncbi.nlm.nih.gov/pubmed/35713888 http://dx.doi.org/10.1002/ejhf.2573 |
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