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Landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated ICU patients
Landiolol is an ultra-short-acting β(1)-selective antagonist developed in Japan that was recently approved for the treatment of tachycardia in intensive care units (ICUs). This study investigated the protective effects of landiolol against the cardiovascular responses during bronchoscopic endotrache...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267460/ https://www.ncbi.nlm.nih.gov/pubmed/25520823 http://dx.doi.org/10.1186/2052-0492-2-6 |
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author | Tochikubo, Junpei Adachi, Yushi U Ejima, Tadashi Numaguchi, Atsushi Matsuda, Naoyuki Sato, Shigehito Shiiya, Norihiko |
author_facet | Tochikubo, Junpei Adachi, Yushi U Ejima, Tadashi Numaguchi, Atsushi Matsuda, Naoyuki Sato, Shigehito Shiiya, Norihiko |
author_sort | Tochikubo, Junpei |
collection | PubMed |
description | Landiolol is an ultra-short-acting β(1)-selective antagonist developed in Japan that was recently approved for the treatment of tachycardia in intensive care units (ICUs). This study investigated the protective effects of landiolol against the cardiovascular responses during bronchoscopic endotracheal suctioning. This study enrolled 15 patients requiring orotracheal intubation in an ICU. All of the patients required endotracheal suctioning using fiber bronchoscopy while sedated at a Ramsay Scale of 2–3. All subsequent suctioning procedures were assigned randomly to three groups using a cross-over design: saline as a placebo (group C) or 20 or 40 μg kg(-1) min(-1) landiolol, respectively (groups L20 and L40). The infusion was started 3 min before bronchoscopy and continued for 6 min. The central venous pressure (CVP) heart rate (HR) and arterial blood pressure (BP) were recorded. Fourteen patients completed the investigation, and 30 procedures (n = 10/group) were analyzed. The suctioning significantly increased the CVP, HR, and BP in groups C and L20, although the changes in BP were of shorter duration in group L20. No significant increase in the hemodynamic parameters was observed in group L40. The administration of landiolol 40 μg kg(-1) min(-1) prevented a harmful hyperdynamic circulatory response to bronchoscopic endotracheal suctioning, without obvious decreases in HR or BP after the intervention. |
format | Online Article Text |
id | pubmed-4267460 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42674602014-12-17 Landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated ICU patients Tochikubo, Junpei Adachi, Yushi U Ejima, Tadashi Numaguchi, Atsushi Matsuda, Naoyuki Sato, Shigehito Shiiya, Norihiko J Intensive Care Letter to the Editor Landiolol is an ultra-short-acting β(1)-selective antagonist developed in Japan that was recently approved for the treatment of tachycardia in intensive care units (ICUs). This study investigated the protective effects of landiolol against the cardiovascular responses during bronchoscopic endotracheal suctioning. This study enrolled 15 patients requiring orotracheal intubation in an ICU. All of the patients required endotracheal suctioning using fiber bronchoscopy while sedated at a Ramsay Scale of 2–3. All subsequent suctioning procedures were assigned randomly to three groups using a cross-over design: saline as a placebo (group C) or 20 or 40 μg kg(-1) min(-1) landiolol, respectively (groups L20 and L40). The infusion was started 3 min before bronchoscopy and continued for 6 min. The central venous pressure (CVP) heart rate (HR) and arterial blood pressure (BP) were recorded. Fourteen patients completed the investigation, and 30 procedures (n = 10/group) were analyzed. The suctioning significantly increased the CVP, HR, and BP in groups C and L20, although the changes in BP were of shorter duration in group L20. No significant increase in the hemodynamic parameters was observed in group L40. The administration of landiolol 40 μg kg(-1) min(-1) prevented a harmful hyperdynamic circulatory response to bronchoscopic endotracheal suctioning, without obvious decreases in HR or BP after the intervention. BioMed Central 2014-01-23 /pmc/articles/PMC4267460/ /pubmed/25520823 http://dx.doi.org/10.1186/2052-0492-2-6 Text en © Tochikubo et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Letter to the Editor Tochikubo, Junpei Adachi, Yushi U Ejima, Tadashi Numaguchi, Atsushi Matsuda, Naoyuki Sato, Shigehito Shiiya, Norihiko Landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated ICU patients |
title | Landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated ICU patients |
title_full | Landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated ICU patients |
title_fullStr | Landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated ICU patients |
title_full_unstemmed | Landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated ICU patients |
title_short | Landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated ICU patients |
title_sort | landiolol reduces hemodynamic responses to bronchoscopy-assisted suctioning in intubated icu patients |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267460/ https://www.ncbi.nlm.nih.gov/pubmed/25520823 http://dx.doi.org/10.1186/2052-0492-2-6 |
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