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Effects of stress ulcer prophylaxis in adult ICU patients receiving renal replacement therapy (Sup-Icu RENal, SIREN): Study protocol for a pre-planned observational study

BACKGROUND: Proton pump inhibitors are often used in critically ill patients to prevent gastrointestinal bleeding despite limited evidence for benefit. Patients with acute kidney injury requiring renal replacement therapy (RRT) are at high risk of gastrointestinal bleeding as (pre-)uremia induces co...

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Autores principales: Schefold, Joerg C., Perner, Anders, Lange, Theis, Wetterslev, Jørn, Wise, Matt P., Borthwick, Mark, Bendel, Stepani, Keus, Frederik, Guttormsen, Anne Berit, Marker, Søren, Krag, Mette, Møller, Morten Hylander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763643/
https://www.ncbi.nlm.nih.gov/pubmed/29321041
http://dx.doi.org/10.1186/s13063-017-2408-3
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author Schefold, Joerg C.
Perner, Anders
Lange, Theis
Wetterslev, Jørn
Wise, Matt P.
Borthwick, Mark
Bendel, Stepani
Keus, Frederik
Guttormsen, Anne Berit
Marker, Søren
Krag, Mette
Møller, Morten Hylander
author_facet Schefold, Joerg C.
Perner, Anders
Lange, Theis
Wetterslev, Jørn
Wise, Matt P.
Borthwick, Mark
Bendel, Stepani
Keus, Frederik
Guttormsen, Anne Berit
Marker, Søren
Krag, Mette
Møller, Morten Hylander
author_sort Schefold, Joerg C.
collection PubMed
description BACKGROUND: Proton pump inhibitors are often used in critically ill patients to prevent gastrointestinal bleeding despite limited evidence for benefit. Patients with acute kidney injury requiring renal replacement therapy (RRT) are at high risk of gastrointestinal bleeding as (pre-)uremia induces coagulopathy through effects on platelets and coagulation cascades. No high-quality randomized clinical trials have previously assessed the benefits and harms of prophylactic proton pump inhibitor use in this high-risk population of adult critically ill patients. METHODS/DESIGN: Among the 3350 patients included in the Stress Ulcer Prophylaxis in the Intensive Care Unit (SUP-ICU) trial—an investigator-initiated international randomized clinical trial on prophylactic proton pump inhibitor versus placebo in acutely admitted adult ICU patients at risk of gastrointestinal bleeding—we will compare the benefits and harms of prophylactic use of proton pump inhibitor in patients in need of RRT versus those not requiring this treatment. We will determine the proportion of patients with clinically important bleeding, the proportion of patients with adverse events including pneumonia, Clostridium difficile enteritis, or acute myocardial ischemia in the ICU, as well as transfusion requirements. Moreover, 90 day and 365 day mortality post-randomization will be investigated. As a secondary analysis, we will examine the association between acute kidney injury and RRT during ICU stay and gastrointestinal bleeding. DISCUSSION: With the outlined predefined analysis, we will characterize the balance between the benefits and harms of stress ulcer prophylaxis in acutely admitted adult ICU patients in need of RRT, including the potential interaction of allocation to proton pump inhibitor versus placebo. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02718261. Registered on 14 March 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-2408-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-57636432018-01-17 Effects of stress ulcer prophylaxis in adult ICU patients receiving renal replacement therapy (Sup-Icu RENal, SIREN): Study protocol for a pre-planned observational study Schefold, Joerg C. Perner, Anders Lange, Theis Wetterslev, Jørn Wise, Matt P. Borthwick, Mark Bendel, Stepani Keus, Frederik Guttormsen, Anne Berit Marker, Søren Krag, Mette Møller, Morten Hylander Trials Study Protocol BACKGROUND: Proton pump inhibitors are often used in critically ill patients to prevent gastrointestinal bleeding despite limited evidence for benefit. Patients with acute kidney injury requiring renal replacement therapy (RRT) are at high risk of gastrointestinal bleeding as (pre-)uremia induces coagulopathy through effects on platelets and coagulation cascades. No high-quality randomized clinical trials have previously assessed the benefits and harms of prophylactic proton pump inhibitor use in this high-risk population of adult critically ill patients. METHODS/DESIGN: Among the 3350 patients included in the Stress Ulcer Prophylaxis in the Intensive Care Unit (SUP-ICU) trial—an investigator-initiated international randomized clinical trial on prophylactic proton pump inhibitor versus placebo in acutely admitted adult ICU patients at risk of gastrointestinal bleeding—we will compare the benefits and harms of prophylactic use of proton pump inhibitor in patients in need of RRT versus those not requiring this treatment. We will determine the proportion of patients with clinically important bleeding, the proportion of patients with adverse events including pneumonia, Clostridium difficile enteritis, or acute myocardial ischemia in the ICU, as well as transfusion requirements. Moreover, 90 day and 365 day mortality post-randomization will be investigated. As a secondary analysis, we will examine the association between acute kidney injury and RRT during ICU stay and gastrointestinal bleeding. DISCUSSION: With the outlined predefined analysis, we will characterize the balance between the benefits and harms of stress ulcer prophylaxis in acutely admitted adult ICU patients in need of RRT, including the potential interaction of allocation to proton pump inhibitor versus placebo. TRIAL REGISTRATION: ClinicalTrials.gov, NCT02718261. Registered on 14 March 2016. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-2408-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-10 /pmc/articles/PMC5763643/ /pubmed/29321041 http://dx.doi.org/10.1186/s13063-017-2408-3 Text en © The Author(s). 2018 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
Schefold, Joerg C.
Perner, Anders
Lange, Theis
Wetterslev, Jørn
Wise, Matt P.
Borthwick, Mark
Bendel, Stepani
Keus, Frederik
Guttormsen, Anne Berit
Marker, Søren
Krag, Mette
Møller, Morten Hylander
Effects of stress ulcer prophylaxis in adult ICU patients receiving renal replacement therapy (Sup-Icu RENal, SIREN): Study protocol for a pre-planned observational study
title Effects of stress ulcer prophylaxis in adult ICU patients receiving renal replacement therapy (Sup-Icu RENal, SIREN): Study protocol for a pre-planned observational study
title_full Effects of stress ulcer prophylaxis in adult ICU patients receiving renal replacement therapy (Sup-Icu RENal, SIREN): Study protocol for a pre-planned observational study
title_fullStr Effects of stress ulcer prophylaxis in adult ICU patients receiving renal replacement therapy (Sup-Icu RENal, SIREN): Study protocol for a pre-planned observational study
title_full_unstemmed Effects of stress ulcer prophylaxis in adult ICU patients receiving renal replacement therapy (Sup-Icu RENal, SIREN): Study protocol for a pre-planned observational study
title_short Effects of stress ulcer prophylaxis in adult ICU patients receiving renal replacement therapy (Sup-Icu RENal, SIREN): Study protocol for a pre-planned observational study
title_sort effects of stress ulcer prophylaxis in adult icu patients receiving renal replacement therapy (sup-icu renal, siren): study protocol for a pre-planned observational study
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763643/
https://www.ncbi.nlm.nih.gov/pubmed/29321041
http://dx.doi.org/10.1186/s13063-017-2408-3
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