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CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices

BACKGROUND: Continuous renal replacement therapy (CRRT) is the recommended modality of dialysis for critically ill patients with hemodynamic instability. Yet there remains significant variability in how CRRT is prescribed and delivered, and limited evidence-basis to guide practice. METHODS: This is...

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Autores principales: Heung, Michael, Bagshaw, Sean M., House, Andrew A., Juncos, Luis A., Piazza, Robin, Goldstein, Stuart L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501006/
https://www.ncbi.nlm.nih.gov/pubmed/28683729
http://dx.doi.org/10.1186/s12882-017-0650-2
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author Heung, Michael
Bagshaw, Sean M.
House, Andrew A.
Juncos, Luis A.
Piazza, Robin
Goldstein, Stuart L.
author_facet Heung, Michael
Bagshaw, Sean M.
House, Andrew A.
Juncos, Luis A.
Piazza, Robin
Goldstein, Stuart L.
author_sort Heung, Michael
collection PubMed
description BACKGROUND: Continuous renal replacement therapy (CRRT) is the recommended modality of dialysis for critically ill patients with hemodynamic instability. Yet there remains significant variability in how CRRT is prescribed and delivered, and limited evidence-basis to guide practice. METHODS: This is a prospective, multi-center observational study of patients undergoing CRRT. Initial enrollment phase will occur at 4 academic medical centers in North America over 5 years, with a target enrollment of 2000 patients. All adult patients (18–89 years of age) receiving CRRT will be eligible for inclusion; patients who undergo CRRT for less than 24 h will be excluded from analysis. Data collection will include patient characteristics at baseline and at time of CRRT initiation; details of CRRT prescription and delivery, including machine-generated treatment data; and patient outcomes. DISCUSSION: The goal of this study is to establish a large comprehensive registry of critically ill adults receiving CRRT. Specific aims include describing variations in CRRT prescription and delivery across quality domains; validating quality measures for CRRT care by correlating processes and outcomes; and establishing a large registry for use in quality improvement and benchmarking efforts. For initial analyses, some particular areas of interest are anticoagulation protocols; approach to fluid overload; CRRT-related workload; and patient safety. TRIAL REGISTRATION: Registered on ClinicalTrials.gov 1/10/2014: NCT02034448.
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spelling pubmed-55010062017-07-10 CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices Heung, Michael Bagshaw, Sean M. House, Andrew A. Juncos, Luis A. Piazza, Robin Goldstein, Stuart L. BMC Nephrol Study Protocol BACKGROUND: Continuous renal replacement therapy (CRRT) is the recommended modality of dialysis for critically ill patients with hemodynamic instability. Yet there remains significant variability in how CRRT is prescribed and delivered, and limited evidence-basis to guide practice. METHODS: This is a prospective, multi-center observational study of patients undergoing CRRT. Initial enrollment phase will occur at 4 academic medical centers in North America over 5 years, with a target enrollment of 2000 patients. All adult patients (18–89 years of age) receiving CRRT will be eligible for inclusion; patients who undergo CRRT for less than 24 h will be excluded from analysis. Data collection will include patient characteristics at baseline and at time of CRRT initiation; details of CRRT prescription and delivery, including machine-generated treatment data; and patient outcomes. DISCUSSION: The goal of this study is to establish a large comprehensive registry of critically ill adults receiving CRRT. Specific aims include describing variations in CRRT prescription and delivery across quality domains; validating quality measures for CRRT care by correlating processes and outcomes; and establishing a large registry for use in quality improvement and benchmarking efforts. For initial analyses, some particular areas of interest are anticoagulation protocols; approach to fluid overload; CRRT-related workload; and patient safety. TRIAL REGISTRATION: Registered on ClinicalTrials.gov 1/10/2014: NCT02034448. BioMed Central 2017-07-06 /pmc/articles/PMC5501006/ /pubmed/28683729 http://dx.doi.org/10.1186/s12882-017-0650-2 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
Heung, Michael
Bagshaw, Sean M.
House, Andrew A.
Juncos, Luis A.
Piazza, Robin
Goldstein, Stuart L.
CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices
title CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices
title_full CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices
title_fullStr CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices
title_full_unstemmed CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices
title_short CRRTnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices
title_sort crrtnet: a prospective, multi-national, observational study of continuous renal replacement therapy practices
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501006/
https://www.ncbi.nlm.nih.gov/pubmed/28683729
http://dx.doi.org/10.1186/s12882-017-0650-2
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