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Pediatric intensive care stress ulcer prevention (PIC-UP): a protocol for a pilot randomized trial
BACKGROUND: Despite sparse pediatric data on effectiveness, the majority of critically ill children receive medications to prevent gastrointestinal (GI) bleeding. Stress ulcer prophylaxis may have unintended consequences—increasing the risk of nosocomial infections—which may be more serious and comm...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438532/ https://www.ncbi.nlm.nih.gov/pubmed/28533916 http://dx.doi.org/10.1186/s40814-017-0142-y |
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author | Duffett, Mark Choong, Karen Foster, Jennifer Gilfoyle, Elaine Lacroix, Jacques Pai, Nikhil Thabane, Lehana Cook, Deborah J |
author_facet | Duffett, Mark Choong, Karen Foster, Jennifer Gilfoyle, Elaine Lacroix, Jacques Pai, Nikhil Thabane, Lehana Cook, Deborah J |
author_sort | Duffett, Mark |
collection | PubMed |
description | BACKGROUND: Despite sparse pediatric data on effectiveness, the majority of critically ill children receive medications to prevent gastrointestinal (GI) bleeding. Stress ulcer prophylaxis may have unintended consequences—increasing the risk of nosocomial infections—which may be more serious and common than the bleeding which these drugs are prescribed to prevent. Randomized controlled trials (RCTs) in pediatric critical care are exceptionally challenging to complete, thus a rigorous pilot RCT is crucial. The objective of this pilot RCT is to assess the feasibility of a large multicentre RCT of stress ulcer prophylaxis with pantoprazole to prevent upper GI bleeding vs. placebo. METHODS: A multi-centre blinded pilot RCT of 120 children in six Canadian PICUs. Children expected to require mechanical ventilation for more than 48 h will be randomized to receive intravenous pantoprazole 1 mg/kg or identical placebo once daily until they no longer need mechanical ventilation. We have four feasibility outcomes and will consider the trial successful if we achieve: 1. Effective screening: If >80% of eligible patients are approached for consent. 2. Timely enrollment: if >80% of participants receive their first dose of the assigned study drug within 1 day of becoming eligible. 3. Participant accrual: If the average monthly enrolment is two or more participants per centre per month. 4. Protocol adherence: if >90% of doses are administered according to the protocol. DISCUSSION: There are many uncertainties about the risks and benefits of stress ulcer prophylaxis. In an era of widespread use—where clinicians prescribe prophylaxis to the more severely ill—a large, rigorous RCT is required. A trial to determine if a strategy of withholding stress ulcer prophylaxis is not inferior to a strategy of routine stress ulcer prophylaxis will be challenging. A carefully designed and implemented pilot trial is essential. TRIAL REGISTRATION: ClinicalTrials.gov:NCT02929563 (Registered October 3, 2016). |
format | Online Article Text |
id | pubmed-5438532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54385322017-05-22 Pediatric intensive care stress ulcer prevention (PIC-UP): a protocol for a pilot randomized trial Duffett, Mark Choong, Karen Foster, Jennifer Gilfoyle, Elaine Lacroix, Jacques Pai, Nikhil Thabane, Lehana Cook, Deborah J Pilot Feasibility Stud Study Protocol BACKGROUND: Despite sparse pediatric data on effectiveness, the majority of critically ill children receive medications to prevent gastrointestinal (GI) bleeding. Stress ulcer prophylaxis may have unintended consequences—increasing the risk of nosocomial infections—which may be more serious and common than the bleeding which these drugs are prescribed to prevent. Randomized controlled trials (RCTs) in pediatric critical care are exceptionally challenging to complete, thus a rigorous pilot RCT is crucial. The objective of this pilot RCT is to assess the feasibility of a large multicentre RCT of stress ulcer prophylaxis with pantoprazole to prevent upper GI bleeding vs. placebo. METHODS: A multi-centre blinded pilot RCT of 120 children in six Canadian PICUs. Children expected to require mechanical ventilation for more than 48 h will be randomized to receive intravenous pantoprazole 1 mg/kg or identical placebo once daily until they no longer need mechanical ventilation. We have four feasibility outcomes and will consider the trial successful if we achieve: 1. Effective screening: If >80% of eligible patients are approached for consent. 2. Timely enrollment: if >80% of participants receive their first dose of the assigned study drug within 1 day of becoming eligible. 3. Participant accrual: If the average monthly enrolment is two or more participants per centre per month. 4. Protocol adherence: if >90% of doses are administered according to the protocol. DISCUSSION: There are many uncertainties about the risks and benefits of stress ulcer prophylaxis. In an era of widespread use—where clinicians prescribe prophylaxis to the more severely ill—a large, rigorous RCT is required. A trial to determine if a strategy of withholding stress ulcer prophylaxis is not inferior to a strategy of routine stress ulcer prophylaxis will be challenging. A carefully designed and implemented pilot trial is essential. TRIAL REGISTRATION: ClinicalTrials.gov:NCT02929563 (Registered October 3, 2016). BioMed Central 2017-05-19 /pmc/articles/PMC5438532/ /pubmed/28533916 http://dx.doi.org/10.1186/s40814-017-0142-y Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 | Study Protocol Duffett, Mark Choong, Karen Foster, Jennifer Gilfoyle, Elaine Lacroix, Jacques Pai, Nikhil Thabane, Lehana Cook, Deborah J Pediatric intensive care stress ulcer prevention (PIC-UP): a protocol for a pilot randomized trial |
title | Pediatric intensive care stress ulcer prevention (PIC-UP): a protocol for a pilot randomized trial |
title_full | Pediatric intensive care stress ulcer prevention (PIC-UP): a protocol for a pilot randomized trial |
title_fullStr | Pediatric intensive care stress ulcer prevention (PIC-UP): a protocol for a pilot randomized trial |
title_full_unstemmed | Pediatric intensive care stress ulcer prevention (PIC-UP): a protocol for a pilot randomized trial |
title_short | Pediatric intensive care stress ulcer prevention (PIC-UP): a protocol for a pilot randomized trial |
title_sort | pediatric intensive care stress ulcer prevention (pic-up): a protocol for a pilot randomized trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5438532/ https://www.ncbi.nlm.nih.gov/pubmed/28533916 http://dx.doi.org/10.1186/s40814-017-0142-y |
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