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Sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial

INTRODUCTION: Not sedating critically ill patients reduces the time patients receive mechanical ventilation, decreases the time in the intensive care department and reduces the total hospital length of stay. We hypothesized that no sedation improves hemodynamic stability, decreases the need for vaso...

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Autores principales: Strøm, Thomas, Johansen, Rasmus R, Prahl, Jens O, Toft, Palle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218972/
https://www.ncbi.nlm.nih.gov/pubmed/21542927
http://dx.doi.org/10.1186/cc10218
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author Strøm, Thomas
Johansen, Rasmus R
Prahl, Jens O
Toft, Palle
author_facet Strøm, Thomas
Johansen, Rasmus R
Prahl, Jens O
Toft, Palle
author_sort Strøm, Thomas
collection PubMed
description INTRODUCTION: Not sedating critically ill patients reduces the time patients receive mechanical ventilation, decreases the time in the intensive care department and reduces the total hospital length of stay. We hypothesized that no sedation improves hemodynamic stability, decreases the need for vasoactive drugs, diminishes the need for extra fluids and lowers the risk of acute kidney injury. METHODS: We performed an evaluation on the database from our previous trial of 140 patients randomized to either no sedation vs. sedation with a daily interruption of sedatives. A total of 113 patients were included in the previous statistical analysis. Ten patients had pre-existing renal impairments and were excluded. Data were collected from observational cards and blood samples. RESULTS: A total of 103 patients were included in this retrospective review. We registered an increased urine output in the group receiving no sedation compared to the sedated control group (1.15 ml/kg/hour (0.59 to 1.53) vs. 0.88 ml/kg/hour (0.052 to 1.26), P = 0.03). In addition we saw a decrease in the number of patients with renal impairment according to the RIFLE classification (indicating Risk of renal dysfunction; Injury to the kidney; Failure of kidney function, Loss of kidney function and End-stage kidney disease) in the group receiving no sedation compared to the sedated control group (25 (51%) vs. 41 (76%), P = 0.012). The difference in the two groups with respect to mean arterial blood pressure, fluid balance and use of vasoactive drugs was not significant. CONCLUSIONS: A no sedation strategy to patients undergoing mechanical ventilation increases the urine output and decreases the number of patients with renal impairments. TRIAL REGISTRATION: ClinicalTrials.gov registration number NCT00466492.
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spelling pubmed-32189722011-11-17 Sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial Strøm, Thomas Johansen, Rasmus R Prahl, Jens O Toft, Palle Crit Care Research INTRODUCTION: Not sedating critically ill patients reduces the time patients receive mechanical ventilation, decreases the time in the intensive care department and reduces the total hospital length of stay. We hypothesized that no sedation improves hemodynamic stability, decreases the need for vasoactive drugs, diminishes the need for extra fluids and lowers the risk of acute kidney injury. METHODS: We performed an evaluation on the database from our previous trial of 140 patients randomized to either no sedation vs. sedation with a daily interruption of sedatives. A total of 113 patients were included in the previous statistical analysis. Ten patients had pre-existing renal impairments and were excluded. Data were collected from observational cards and blood samples. RESULTS: A total of 103 patients were included in this retrospective review. We registered an increased urine output in the group receiving no sedation compared to the sedated control group (1.15 ml/kg/hour (0.59 to 1.53) vs. 0.88 ml/kg/hour (0.052 to 1.26), P = 0.03). In addition we saw a decrease in the number of patients with renal impairment according to the RIFLE classification (indicating Risk of renal dysfunction; Injury to the kidney; Failure of kidney function, Loss of kidney function and End-stage kidney disease) in the group receiving no sedation compared to the sedated control group (25 (51%) vs. 41 (76%), P = 0.012). The difference in the two groups with respect to mean arterial blood pressure, fluid balance and use of vasoactive drugs was not significant. CONCLUSIONS: A no sedation strategy to patients undergoing mechanical ventilation increases the urine output and decreases the number of patients with renal impairments. TRIAL REGISTRATION: ClinicalTrials.gov registration number NCT00466492. BioMed Central 2011 2011-05-04 /pmc/articles/PMC3218972/ /pubmed/21542927 http://dx.doi.org/10.1186/cc10218 Text en Copyright ©2011 Strøm et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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.
spellingShingle Research
Strøm, Thomas
Johansen, Rasmus R
Prahl, Jens O
Toft, Palle
Sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial
title Sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial
title_full Sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial
title_fullStr Sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial
title_full_unstemmed Sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial
title_short Sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial
title_sort sedation and renal impairment in critically ill patients: a post hoc analysis of a randomized trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3218972/
https://www.ncbi.nlm.nih.gov/pubmed/21542927
http://dx.doi.org/10.1186/cc10218
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