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Haemodynamic Effects of Sacubitril/Valsartan Initiation in Outpatients with Chronic Heart Failure
BACKGROUND: Sacubitril/valsartan (S/V) improves outcomes in patients with heart failure with reduced ejection fraction (HFrEF). Data about the immediate, short-, and intermediate-term hemodynamic effects of S/V are limited. METHODS: In this prospective observational study, 37 outpatients with chroni...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493168/ https://www.ncbi.nlm.nih.gov/pubmed/36136241 http://dx.doi.org/10.1007/s40256-022-00549-2 |
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author | Fröhlich, Hanna Frey, Norbert Estler, Bent Mäck, Mirjam Schlegel, Philipp Beckendorf, Jan Frankenstein, Lutz Täger, Tobias |
author_facet | Fröhlich, Hanna Frey, Norbert Estler, Bent Mäck, Mirjam Schlegel, Philipp Beckendorf, Jan Frankenstein, Lutz Täger, Tobias |
author_sort | Fröhlich, Hanna |
collection | PubMed |
description | BACKGROUND: Sacubitril/valsartan (S/V) improves outcomes in patients with heart failure with reduced ejection fraction (HFrEF). Data about the immediate, short-, and intermediate-term hemodynamic effects of S/V are limited. METHODS: In this prospective observational study, 37 outpatients with chronic HFrEF were treated with S/V according to current guideline recommendations. Next to clinical, laboratory and echocardiographic parameters, haemodynamic variables were assessed non-invasively by use of inert gas rebreathing and bioimpedance cardiography at baseline and at 2-week, 3-month and 6-month follow-up. The course of variables throughout the study and the relationship between variables were analysed using fractional polynomials. RESULTS: S/V treatment resulted in short- and intermediate-term improvements in NYHA functional class (2.3 ± 0.6 at baseline vs. 1.9 ± 0.5 at 6-month follow-up, p = 0.14), 6-min walk test (453 ± 110 vs. 528 ± 98 m, p = 0.02), ejection fraction (31 ± 9 vs. 36 ± 12%, p = 0.13), pulmonary artery pressure (39 ± 10 vs. 31 ± 10 mmHg, p = 0.02), and NT-proBNP values (1702 (782–2897 vs. 1004 (599–1627) ng/L, p = 0.03). In addition, S/V caused immediate decreases in systemic vascular resistance index (SVRI) and systolic blood pressure (SBP), which were associated with a simultaneous drop in stroke volume (SV) and cardiac index (CI). However, while SVRI and SBP remained at low levels during further treatment, SV and CI restored rapidly and increased to slightly higher levels thereafter. CONCLUSION: The vasodilative effects of S/V result in immediate reductions in SVRI, SBP, SV and CI. However, S/V induces reverse cardiac remodelling, which is apparent shortly after treatment initiation and leads to improvements of clinical, functional, echocardiographic, laboratory and haemodynamic variables. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40256-022-00549-2. |
format | Online Article Text |
id | pubmed-9493168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-94931682022-09-22 Haemodynamic Effects of Sacubitril/Valsartan Initiation in Outpatients with Chronic Heart Failure Fröhlich, Hanna Frey, Norbert Estler, Bent Mäck, Mirjam Schlegel, Philipp Beckendorf, Jan Frankenstein, Lutz Täger, Tobias Am J Cardiovasc Drugs Original Research Article BACKGROUND: Sacubitril/valsartan (S/V) improves outcomes in patients with heart failure with reduced ejection fraction (HFrEF). Data about the immediate, short-, and intermediate-term hemodynamic effects of S/V are limited. METHODS: In this prospective observational study, 37 outpatients with chronic HFrEF were treated with S/V according to current guideline recommendations. Next to clinical, laboratory and echocardiographic parameters, haemodynamic variables were assessed non-invasively by use of inert gas rebreathing and bioimpedance cardiography at baseline and at 2-week, 3-month and 6-month follow-up. The course of variables throughout the study and the relationship between variables were analysed using fractional polynomials. RESULTS: S/V treatment resulted in short- and intermediate-term improvements in NYHA functional class (2.3 ± 0.6 at baseline vs. 1.9 ± 0.5 at 6-month follow-up, p = 0.14), 6-min walk test (453 ± 110 vs. 528 ± 98 m, p = 0.02), ejection fraction (31 ± 9 vs. 36 ± 12%, p = 0.13), pulmonary artery pressure (39 ± 10 vs. 31 ± 10 mmHg, p = 0.02), and NT-proBNP values (1702 (782–2897 vs. 1004 (599–1627) ng/L, p = 0.03). In addition, S/V caused immediate decreases in systemic vascular resistance index (SVRI) and systolic blood pressure (SBP), which were associated with a simultaneous drop in stroke volume (SV) and cardiac index (CI). However, while SVRI and SBP remained at low levels during further treatment, SV and CI restored rapidly and increased to slightly higher levels thereafter. CONCLUSION: The vasodilative effects of S/V result in immediate reductions in SVRI, SBP, SV and CI. However, S/V induces reverse cardiac remodelling, which is apparent shortly after treatment initiation and leads to improvements of clinical, functional, echocardiographic, laboratory and haemodynamic variables. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40256-022-00549-2. Springer International Publishing 2022-09-22 2022 /pmc/articles/PMC9493168/ /pubmed/36136241 http://dx.doi.org/10.1007/s40256-022-00549-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Research Article Fröhlich, Hanna Frey, Norbert Estler, Bent Mäck, Mirjam Schlegel, Philipp Beckendorf, Jan Frankenstein, Lutz Täger, Tobias Haemodynamic Effects of Sacubitril/Valsartan Initiation in Outpatients with Chronic Heart Failure |
title | Haemodynamic Effects of Sacubitril/Valsartan Initiation in Outpatients with Chronic Heart Failure |
title_full | Haemodynamic Effects of Sacubitril/Valsartan Initiation in Outpatients with Chronic Heart Failure |
title_fullStr | Haemodynamic Effects of Sacubitril/Valsartan Initiation in Outpatients with Chronic Heart Failure |
title_full_unstemmed | Haemodynamic Effects of Sacubitril/Valsartan Initiation in Outpatients with Chronic Heart Failure |
title_short | Haemodynamic Effects of Sacubitril/Valsartan Initiation in Outpatients with Chronic Heart Failure |
title_sort | haemodynamic effects of sacubitril/valsartan initiation in outpatients with chronic heart failure |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9493168/ https://www.ncbi.nlm.nih.gov/pubmed/36136241 http://dx.doi.org/10.1007/s40256-022-00549-2 |
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