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Effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension

A relevant number of patients with resistant hypertension do not achieve blood pressure (BP) dipping during nighttime. This inadequate nocturnal BP reduction is associated with elevated cardiovascular risks. The aim of this study was to evaluate whether a nighttime intensification of BAT might impro...

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Autores principales: Wallbach, Manuel, Born, Ellen, Schäfer, Ann‐Kathrin, Koziolek, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832236/
https://www.ncbi.nlm.nih.gov/pubmed/36545753
http://dx.doi.org/10.1111/jch.14620
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author Wallbach, Manuel
Born, Ellen
Schäfer, Ann‐Kathrin
Koziolek, Michael J.
author_facet Wallbach, Manuel
Born, Ellen
Schäfer, Ann‐Kathrin
Koziolek, Michael J.
author_sort Wallbach, Manuel
collection PubMed
description A relevant number of patients with resistant hypertension do not achieve blood pressure (BP) dipping during nighttime. This inadequate nocturnal BP reduction is associated with elevated cardiovascular risks. The aim of this study was to evaluate whether a nighttime intensification of BAT might improve nocturnal BP dipping. In this prospective observational study, non‐dippers treated with BAT for at least 6 months were included. BAT programming was modified in a two‐step intensification of nighttime stimulation at baseline and week 6. Twenty‐four hours ambulatory BP (ABP) was measured at inclusion and after 3 months. A number of 24 patients with non‐ or inverted dipping pattern, treated with BAT for a median of 44 months (IQR 25–52) were included. At baseline of the study, patients were 66 ± 9 years old, had a BMI of 33 ± 6 kg/m(2), showed an office BP of 135 ± 22/72 ± 10 mmHg, and took a median number of antihypertensives of 6 (IQR 4–9). Nighttime stimulation of BAT was adapted by an intensification of pulse width from 237 ± 161 to 267 ± 170 μs (p = .003) while frequency (p = .10) and amplitude (p = .95) remained unchanged. Uptitration of BAT programming resulted in an increase of systolic dipping from 2 ± 6 to 6 ± 8% (p = .03) accompanied with a significant improvement of dipping pattern (p = .02). Twenty four hours ABP, day‐ and nighttime ABP remained unchanged. Programming of an intensified nighttime BAT interval improved dipping profile in patients treated with BAT, while the overall 24 h ABP did not change. Whether the improved dipping response contributes to a reduction of cardiovascular risk beyond the BP‐lowering effects of BAT, however, remains to be shown.
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spelling pubmed-98322362023-01-12 Effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension Wallbach, Manuel Born, Ellen Schäfer, Ann‐Kathrin Koziolek, Michael J. J Clin Hypertens (Greenwich) Clinical Trial A relevant number of patients with resistant hypertension do not achieve blood pressure (BP) dipping during nighttime. This inadequate nocturnal BP reduction is associated with elevated cardiovascular risks. The aim of this study was to evaluate whether a nighttime intensification of BAT might improve nocturnal BP dipping. In this prospective observational study, non‐dippers treated with BAT for at least 6 months were included. BAT programming was modified in a two‐step intensification of nighttime stimulation at baseline and week 6. Twenty‐four hours ambulatory BP (ABP) was measured at inclusion and after 3 months. A number of 24 patients with non‐ or inverted dipping pattern, treated with BAT for a median of 44 months (IQR 25–52) were included. At baseline of the study, patients were 66 ± 9 years old, had a BMI of 33 ± 6 kg/m(2), showed an office BP of 135 ± 22/72 ± 10 mmHg, and took a median number of antihypertensives of 6 (IQR 4–9). Nighttime stimulation of BAT was adapted by an intensification of pulse width from 237 ± 161 to 267 ± 170 μs (p = .003) while frequency (p = .10) and amplitude (p = .95) remained unchanged. Uptitration of BAT programming resulted in an increase of systolic dipping from 2 ± 6 to 6 ± 8% (p = .03) accompanied with a significant improvement of dipping pattern (p = .02). Twenty four hours ABP, day‐ and nighttime ABP remained unchanged. Programming of an intensified nighttime BAT interval improved dipping profile in patients treated with BAT, while the overall 24 h ABP did not change. Whether the improved dipping response contributes to a reduction of cardiovascular risk beyond the BP‐lowering effects of BAT, however, remains to be shown. John Wiley and Sons Inc. 2022-12-21 /pmc/articles/PMC9832236/ /pubmed/36545753 http://dx.doi.org/10.1111/jch.14620 Text en © 2022 The Authors. The Journal of Clinical Hypertension published by Wiley Periodicals LLC. 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 Clinical Trial
Wallbach, Manuel
Born, Ellen
Schäfer, Ann‐Kathrin
Koziolek, Michael J.
Effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension
title Effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension
title_full Effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension
title_fullStr Effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension
title_full_unstemmed Effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension
title_short Effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension
title_sort effect of baroreflex activation therapy on dipping pattern in patients with resistant hypertension
topic Clinical Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832236/
https://www.ncbi.nlm.nih.gov/pubmed/36545753
http://dx.doi.org/10.1111/jch.14620
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