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Levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study
INTRODUCTION: The purpose of the present study was to investigate microcirculatory blood flow in patients with septic shock treated with levosimendan as compared to an active comparator drug (i.e. dobutamine). The primary end point was a difference of ≥ 20% in the microvascular flow index of small v...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219978/ https://www.ncbi.nlm.nih.gov/pubmed/21182783 http://dx.doi.org/10.1186/cc9387 |
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author | Morelli, Andrea Donati, Abele Ertmer, Christian Rehberg, Sebastian Lange, Matthias Orecchioni, Alessandra Cecchini, Valeria Landoni, Giovanni Pelaia, Paolo Pietropaoli, Paolo Van Aken, Hugo Teboul, Jean-Louis Ince, Can Westphal, Martin |
author_facet | Morelli, Andrea Donati, Abele Ertmer, Christian Rehberg, Sebastian Lange, Matthias Orecchioni, Alessandra Cecchini, Valeria Landoni, Giovanni Pelaia, Paolo Pietropaoli, Paolo Van Aken, Hugo Teboul, Jean-Louis Ince, Can Westphal, Martin |
author_sort | Morelli, Andrea |
collection | PubMed |
description | INTRODUCTION: The purpose of the present study was to investigate microcirculatory blood flow in patients with septic shock treated with levosimendan as compared to an active comparator drug (i.e. dobutamine). The primary end point was a difference of ≥ 20% in the microvascular flow index of small vessels (MFIs) among groups. METHODS: The study was designed as a prospective, randomized, double-blind clinical trial and performed in a multidisciplinary intensive care unit. After achieving normovolemia and a mean arterial pressure of at least 65 mmHg, 40 septic shock patients were randomized to receive either levosimendan 0.2 μg·kg(-1)·min(-1 )(n = 20) or an active comparator (dobutamine 5 μg·kg(-1)·min(-1); control; n = 20) for 24 hours. Sublingual microcirculatory blood flow of small and medium vessels was assessed by sidestream dark-field imaging. Microcirculatory variables and data from right heart catheterization were obtained at baseline and 24 hours after randomization. Baseline and demographic data were compared by means of Mann-Whitney rank sum test or chi-square test, as appropriate. Microvascular and hemodynamic variables were analyzed using the Mann-Whitney rank sum test. RESULTS: Microcirculatory flow indices of small and medium vessels increased over time and were significantly higher in the levosimendan group as compared to the control group (24 hrs: MFIm 3.0 (3.0; 3.0) vs. 2.9 (2.8; 3.0); P = .02; MFIs 2.9 (2.9; 3.0) vs. 2.7 (2.3; 2.8); P < .001). The relative increase of perfused vessel density vs. baseline was significantly higher in the levosimendan group than in the control group (dMFIm 10 (3; 23)% vs. 0 (-1; 9)%; P = .007; dMFIs 47 (26; 83)% vs. 10 (-3; 27); P < .001). In addition, the heterogeneity index decreased only in the levosimendan group (dHI -93 (-100; -84)% vs. 0 (-78; 57)%; P < .001). There was no statistically significant correlation between systemic and microcirculatory flow variables within each group (each P > .05). CONCLUSIONS: Compared to a standard dose of 5 μg·kg(-1)·min(-1 )of dobutamine, levosimendan at 0.2 μg·kg(-1)·min(-1 )improved sublingual microcirculatory blood flow in patients with septic shock, as reflected by changes in microcirculatory flow indices of small and medium vessels. TRIAL REGISTRATION: NCT00800306. |
format | Online Article Text |
id | pubmed-3219978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32199782011-11-18 Levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study Morelli, Andrea Donati, Abele Ertmer, Christian Rehberg, Sebastian Lange, Matthias Orecchioni, Alessandra Cecchini, Valeria Landoni, Giovanni Pelaia, Paolo Pietropaoli, Paolo Van Aken, Hugo Teboul, Jean-Louis Ince, Can Westphal, Martin Crit Care Research INTRODUCTION: The purpose of the present study was to investigate microcirculatory blood flow in patients with septic shock treated with levosimendan as compared to an active comparator drug (i.e. dobutamine). The primary end point was a difference of ≥ 20% in the microvascular flow index of small vessels (MFIs) among groups. METHODS: The study was designed as a prospective, randomized, double-blind clinical trial and performed in a multidisciplinary intensive care unit. After achieving normovolemia and a mean arterial pressure of at least 65 mmHg, 40 septic shock patients were randomized to receive either levosimendan 0.2 μg·kg(-1)·min(-1 )(n = 20) or an active comparator (dobutamine 5 μg·kg(-1)·min(-1); control; n = 20) for 24 hours. Sublingual microcirculatory blood flow of small and medium vessels was assessed by sidestream dark-field imaging. Microcirculatory variables and data from right heart catheterization were obtained at baseline and 24 hours after randomization. Baseline and demographic data were compared by means of Mann-Whitney rank sum test or chi-square test, as appropriate. Microvascular and hemodynamic variables were analyzed using the Mann-Whitney rank sum test. RESULTS: Microcirculatory flow indices of small and medium vessels increased over time and were significantly higher in the levosimendan group as compared to the control group (24 hrs: MFIm 3.0 (3.0; 3.0) vs. 2.9 (2.8; 3.0); P = .02; MFIs 2.9 (2.9; 3.0) vs. 2.7 (2.3; 2.8); P < .001). The relative increase of perfused vessel density vs. baseline was significantly higher in the levosimendan group than in the control group (dMFIm 10 (3; 23)% vs. 0 (-1; 9)%; P = .007; dMFIs 47 (26; 83)% vs. 10 (-3; 27); P < .001). In addition, the heterogeneity index decreased only in the levosimendan group (dHI -93 (-100; -84)% vs. 0 (-78; 57)%; P < .001). There was no statistically significant correlation between systemic and microcirculatory flow variables within each group (each P > .05). CONCLUSIONS: Compared to a standard dose of 5 μg·kg(-1)·min(-1 )of dobutamine, levosimendan at 0.2 μg·kg(-1)·min(-1 )improved sublingual microcirculatory blood flow in patients with septic shock, as reflected by changes in microcirculatory flow indices of small and medium vessels. TRIAL REGISTRATION: NCT00800306. BioMed Central 2010 2010-12-23 /pmc/articles/PMC3219978/ /pubmed/21182783 http://dx.doi.org/10.1186/cc9387 Text en Copyright ©2010 Morelli et al.; licensee BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Morelli, Andrea Donati, Abele Ertmer, Christian Rehberg, Sebastian Lange, Matthias Orecchioni, Alessandra Cecchini, Valeria Landoni, Giovanni Pelaia, Paolo Pietropaoli, Paolo Van Aken, Hugo Teboul, Jean-Louis Ince, Can Westphal, Martin Levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study |
title | Levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study |
title_full | Levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study |
title_fullStr | Levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study |
title_full_unstemmed | Levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study |
title_short | Levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study |
title_sort | levosimendan for resuscitating the microcirculation in patients with septic shock: a randomized controlled study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219978/ https://www.ncbi.nlm.nih.gov/pubmed/21182783 http://dx.doi.org/10.1186/cc9387 |
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