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Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial

INTRODUCTION: The aim of this study was to assess the effect of low-dose corticosteroid therapy in reducing shock duration after severe burn. METHODS: A placebo-controlled, double-blind, randomized clinical trial (RCT) was performed on two parallel groups in the burn intensive care unit (ICU). Patie...

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Autores principales: Venet, Fabienne, Plassais, Jonathan, Textoris, Julien, Cazalis, Marie-Angélique, Pachot, Alexandre, Bertin-Maghit, Marc, Magnin, Christophe, Rimmelé, Thomas, Monneret, Guillaume, Tissot, Sylvie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347659/
https://www.ncbi.nlm.nih.gov/pubmed/25619170
http://dx.doi.org/10.1186/s13054-015-0740-0
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author Venet, Fabienne
Plassais, Jonathan
Textoris, Julien
Cazalis, Marie-Angélique
Pachot, Alexandre
Bertin-Maghit, Marc
Magnin, Christophe
Rimmelé, Thomas
Monneret, Guillaume
Tissot, Sylvie
author_facet Venet, Fabienne
Plassais, Jonathan
Textoris, Julien
Cazalis, Marie-Angélique
Pachot, Alexandre
Bertin-Maghit, Marc
Magnin, Christophe
Rimmelé, Thomas
Monneret, Guillaume
Tissot, Sylvie
author_sort Venet, Fabienne
collection PubMed
description INTRODUCTION: The aim of this study was to assess the effect of low-dose corticosteroid therapy in reducing shock duration after severe burn. METHODS: A placebo-controlled, double-blind, randomized clinical trial (RCT) was performed on two parallel groups in the burn intensive care unit (ICU). Patients were randomized to receive either low-dose corticosteroid therapy or placebo for seven days. A corticotropin test was performed at the time of randomization, before the administration of the treatment dose. Thirty-two severely burned patients with refractory shock (>0.5 μg/kg/min of norepinephrine) were prospectively included in the study. RESULTS: We included 12 patients in the hydrocortisone-treated group and 15 patients in the placebo group in the final analysis. Among these patients, 21 were nonresponders to the corticotropin test. Median norepinephrine treatment duration (primary objective) was significantly lower in the corticosteroid-treated versus the placebo group (57 hours versus 120 hours, P = 0.035). The number of patients without norepinephrine 72 hours after inclusion was significantly lower in the treated group (P = 0.003, log-rank test analysis). The total quantities of norepinephrine administered to patients were lower in the hydrocortisone-treated versus the placebo group (1,205 μg/kg (1,079 to 2,167) versus 1,971 μg/kg (1,535 to 3,893), P = 0.067). There was no difference in terms of ICU or hospital length of stay, sepsis incidence, cicatrization or mortality. CONCLUSIONS: In this placebo-controlled, randomized, double-blind clinical trial, we show for the first time that the administration of low-dose hydrocortisone in burn patients with severe shock reduces vasopressor administration. TRIAL REGISTRATION: Clinicaltrial.gov NCT00149123. Registered 6 September 2005. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-015-0740-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-43476592015-03-04 Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial Venet, Fabienne Plassais, Jonathan Textoris, Julien Cazalis, Marie-Angélique Pachot, Alexandre Bertin-Maghit, Marc Magnin, Christophe Rimmelé, Thomas Monneret, Guillaume Tissot, Sylvie Crit Care Research INTRODUCTION: The aim of this study was to assess the effect of low-dose corticosteroid therapy in reducing shock duration after severe burn. METHODS: A placebo-controlled, double-blind, randomized clinical trial (RCT) was performed on two parallel groups in the burn intensive care unit (ICU). Patients were randomized to receive either low-dose corticosteroid therapy or placebo for seven days. A corticotropin test was performed at the time of randomization, before the administration of the treatment dose. Thirty-two severely burned patients with refractory shock (>0.5 μg/kg/min of norepinephrine) were prospectively included in the study. RESULTS: We included 12 patients in the hydrocortisone-treated group and 15 patients in the placebo group in the final analysis. Among these patients, 21 were nonresponders to the corticotropin test. Median norepinephrine treatment duration (primary objective) was significantly lower in the corticosteroid-treated versus the placebo group (57 hours versus 120 hours, P = 0.035). The number of patients without norepinephrine 72 hours after inclusion was significantly lower in the treated group (P = 0.003, log-rank test analysis). The total quantities of norepinephrine administered to patients were lower in the hydrocortisone-treated versus the placebo group (1,205 μg/kg (1,079 to 2,167) versus 1,971 μg/kg (1,535 to 3,893), P = 0.067). There was no difference in terms of ICU or hospital length of stay, sepsis incidence, cicatrization or mortality. CONCLUSIONS: In this placebo-controlled, randomized, double-blind clinical trial, we show for the first time that the administration of low-dose hydrocortisone in burn patients with severe shock reduces vasopressor administration. TRIAL REGISTRATION: Clinicaltrial.gov NCT00149123. Registered 6 September 2005. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13054-015-0740-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-26 2015 /pmc/articles/PMC4347659/ /pubmed/25619170 http://dx.doi.org/10.1186/s13054-015-0740-0 Text en © Venet et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Research
Venet, Fabienne
Plassais, Jonathan
Textoris, Julien
Cazalis, Marie-Angélique
Pachot, Alexandre
Bertin-Maghit, Marc
Magnin, Christophe
Rimmelé, Thomas
Monneret, Guillaume
Tissot, Sylvie
Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial
title Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial
title_full Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial
title_fullStr Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial
title_full_unstemmed Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial
title_short Low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial
title_sort low-dose hydrocortisone reduces norepinephrine duration in severe burn patients: a randomized clinical trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347659/
https://www.ncbi.nlm.nih.gov/pubmed/25619170
http://dx.doi.org/10.1186/s13054-015-0740-0
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