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Daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial

BACKGROUND: In adult patients who are critically ill and mechanically ventilated, daily interruption of sedation (DSI) is an effective method of improving sedation management, resulting in a decrease of the duration of mechanical ventilation, the length of stay in the intensive care unit (ICU) and t...

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Autores principales: Vet, Nienke J, de Wildt, Saskia N, Verlaat, Carin WM, Knibbe, Catherijne AJ, Mooij, Miriam G, Hop, Wim CJ, van Rosmalen, Joost, Tibboel, Dick, de Hoog, Matthijs
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928607/
https://www.ncbi.nlm.nih.gov/pubmed/24524204
http://dx.doi.org/10.1186/1745-6215-15-55
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author Vet, Nienke J
de Wildt, Saskia N
Verlaat, Carin WM
Knibbe, Catherijne AJ
Mooij, Miriam G
Hop, Wim CJ
van Rosmalen, Joost
Tibboel, Dick
de Hoog, Matthijs
author_facet Vet, Nienke J
de Wildt, Saskia N
Verlaat, Carin WM
Knibbe, Catherijne AJ
Mooij, Miriam G
Hop, Wim CJ
van Rosmalen, Joost
Tibboel, Dick
de Hoog, Matthijs
author_sort Vet, Nienke J
collection PubMed
description BACKGROUND: In adult patients who are critically ill and mechanically ventilated, daily interruption of sedation (DSI) is an effective method of improving sedation management, resulting in a decrease of the duration of mechanical ventilation, the length of stay in the intensive care unit (ICU) and the length of stay in the hospital. It is a safe and effective approach and is common practice in adult ICUs. For critically ill children it is unknown if DSI is effective and feasible. The aim of this multicenter randomized controlled trial is to evaluate the safety and efficacy of daily sedation interruption in critically ill children. METHODS/DESIGN: Children between 0 and 18 years of age who require mechanical ventilation, with an expected duration of at least 48 h and need for sedative infusion, will be included. After enrollment patients will be randomly assigned to DSI in combination with protocolized sedation (intervention group) or protocolized continuous sedation (control group). A sedation protocol that contains an algorithm for increasing and weaning of sedatives and analgesics will be used. The sedative infusion will be restarted if the patient becomes uncomfortable or agitated according to the sedation protocol. The primary endpoint is the number of ventilator-free days at 28 days. TRIAL REGISTRATION: NTR2030
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spelling pubmed-39286072014-02-20 Daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial Vet, Nienke J de Wildt, Saskia N Verlaat, Carin WM Knibbe, Catherijne AJ Mooij, Miriam G Hop, Wim CJ van Rosmalen, Joost Tibboel, Dick de Hoog, Matthijs Trials Study Protocol BACKGROUND: In adult patients who are critically ill and mechanically ventilated, daily interruption of sedation (DSI) is an effective method of improving sedation management, resulting in a decrease of the duration of mechanical ventilation, the length of stay in the intensive care unit (ICU) and the length of stay in the hospital. It is a safe and effective approach and is common practice in adult ICUs. For critically ill children it is unknown if DSI is effective and feasible. The aim of this multicenter randomized controlled trial is to evaluate the safety and efficacy of daily sedation interruption in critically ill children. METHODS/DESIGN: Children between 0 and 18 years of age who require mechanical ventilation, with an expected duration of at least 48 h and need for sedative infusion, will be included. After enrollment patients will be randomly assigned to DSI in combination with protocolized sedation (intervention group) or protocolized continuous sedation (control group). A sedation protocol that contains an algorithm for increasing and weaning of sedatives and analgesics will be used. The sedative infusion will be restarted if the patient becomes uncomfortable or agitated according to the sedation protocol. The primary endpoint is the number of ventilator-free days at 28 days. TRIAL REGISTRATION: NTR2030 BioMed Central 2014-02-13 /pmc/articles/PMC3928607/ /pubmed/24524204 http://dx.doi.org/10.1186/1745-6215-15-55 Text en Copyright © 2014 Vet 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 credited.
spellingShingle Study Protocol
Vet, Nienke J
de Wildt, Saskia N
Verlaat, Carin WM
Knibbe, Catherijne AJ
Mooij, Miriam G
Hop, Wim CJ
van Rosmalen, Joost
Tibboel, Dick
de Hoog, Matthijs
Daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial
title Daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial
title_full Daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial
title_fullStr Daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial
title_full_unstemmed Daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial
title_short Daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial
title_sort daily interruption of sedation in critically ill children: study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928607/
https://www.ncbi.nlm.nih.gov/pubmed/24524204
http://dx.doi.org/10.1186/1745-6215-15-55
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