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Lung Ultrasound Guided Fluid Management Protocol for the Critically Ill Patient: study protocol for a multi-centre randomized controlled trial
BACKGROUND: In routine intensive care unit (ICU) practice, fluids are often administered without a safety limit, which may lead to fluid overload and decreased survival. Recently, B-lines score (BLS) has been validated as a lung ultrasound (LUS) quantification of pulmonary congestion. This suggests...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482502/ https://www.ncbi.nlm.nih.gov/pubmed/31023358 http://dx.doi.org/10.1186/s13063-019-3345-0 |
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author | Rusu, Daniel-Mihai Siriopol, Ianis Grigoras, Ioana Blaj, Mihaela Ciumanghel, Adi-Ionut Siriopol, Dimitrie Nistor, Ionut Onofriescu, Mihai Sandu, Gigel Cobzaru, Beatrice Scripcariu, Dragos Viorel Diaconu, Olguta Covic, Adrian Constantin |
author_facet | Rusu, Daniel-Mihai Siriopol, Ianis Grigoras, Ioana Blaj, Mihaela Ciumanghel, Adi-Ionut Siriopol, Dimitrie Nistor, Ionut Onofriescu, Mihai Sandu, Gigel Cobzaru, Beatrice Scripcariu, Dragos Viorel Diaconu, Olguta Covic, Adrian Constantin |
author_sort | Rusu, Daniel-Mihai |
collection | PubMed |
description | BACKGROUND: In routine intensive care unit (ICU) practice, fluids are often administered without a safety limit, which may lead to fluid overload and decreased survival. Recently, B-lines score (BLS) has been validated as a lung ultrasound (LUS) quantification of pulmonary congestion. This suggests that LUS may provide a safety threshold to conduct fluid therapy and to avoid overhydration. However, there is no randomized study to test the utility of LUS in guiding fluid management in ICU patients by using a pre-specified BLS cut-off value as a threshold for fluid removal. METHODS: LUS Guided Fluid Management Protocol for the Critically Ill Patient is a prospective, multi-centre, randomized controlled trial. Five hundred ICU patients will be randomly assigned in a 1:1 ratio, to protocolized LUS-based fluid management or usual care. The trial intervention will start on ICU admission and will consist in daily assessment of BLS and triggered evacuation of excessive fluids with loop diuretics (Furosemide) when BLS ≥ 15. If rebalancing volume status with diuretics fails, forced evacuation by ultrafiltration will be used. The main endpoint is death from all causes at 28 days from randomization. The secondary outcomes are presence and time-course evolution of organ dysfunctions, ICU- and hospital length of stay, all-cause mortality at 90 days, and health economics data. DISCUSSION: If study results will show that LUS guided fluid management protocol improves outcome in ICU patients, it will be the base for other studies to refine this protocol or track those categories of critically ill patients to whom it may bring maximum benefits. TRIAL REGISTRATION: ClinicalTrials.gov, NCT03393065. Registered on 8 January 2018. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-019-3345-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6482502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64825022019-05-02 Lung Ultrasound Guided Fluid Management Protocol for the Critically Ill Patient: study protocol for a multi-centre randomized controlled trial Rusu, Daniel-Mihai Siriopol, Ianis Grigoras, Ioana Blaj, Mihaela Ciumanghel, Adi-Ionut Siriopol, Dimitrie Nistor, Ionut Onofriescu, Mihai Sandu, Gigel Cobzaru, Beatrice Scripcariu, Dragos Viorel Diaconu, Olguta Covic, Adrian Constantin Trials Study Protocol BACKGROUND: In routine intensive care unit (ICU) practice, fluids are often administered without a safety limit, which may lead to fluid overload and decreased survival. Recently, B-lines score (BLS) has been validated as a lung ultrasound (LUS) quantification of pulmonary congestion. This suggests that LUS may provide a safety threshold to conduct fluid therapy and to avoid overhydration. However, there is no randomized study to test the utility of LUS in guiding fluid management in ICU patients by using a pre-specified BLS cut-off value as a threshold for fluid removal. METHODS: LUS Guided Fluid Management Protocol for the Critically Ill Patient is a prospective, multi-centre, randomized controlled trial. Five hundred ICU patients will be randomly assigned in a 1:1 ratio, to protocolized LUS-based fluid management or usual care. The trial intervention will start on ICU admission and will consist in daily assessment of BLS and triggered evacuation of excessive fluids with loop diuretics (Furosemide) when BLS ≥ 15. If rebalancing volume status with diuretics fails, forced evacuation by ultrafiltration will be used. The main endpoint is death from all causes at 28 days from randomization. The secondary outcomes are presence and time-course evolution of organ dysfunctions, ICU- and hospital length of stay, all-cause mortality at 90 days, and health economics data. DISCUSSION: If study results will show that LUS guided fluid management protocol improves outcome in ICU patients, it will be the base for other studies to refine this protocol or track those categories of critically ill patients to whom it may bring maximum benefits. TRIAL REGISTRATION: ClinicalTrials.gov, NCT03393065. Registered on 8 January 2018. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13063-019-3345-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-25 /pmc/articles/PMC6482502/ /pubmed/31023358 http://dx.doi.org/10.1186/s13063-019-3345-0 Text en © The Author(s). 2019 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 Rusu, Daniel-Mihai Siriopol, Ianis Grigoras, Ioana Blaj, Mihaela Ciumanghel, Adi-Ionut Siriopol, Dimitrie Nistor, Ionut Onofriescu, Mihai Sandu, Gigel Cobzaru, Beatrice Scripcariu, Dragos Viorel Diaconu, Olguta Covic, Adrian Constantin Lung Ultrasound Guided Fluid Management Protocol for the Critically Ill Patient: study protocol for a multi-centre randomized controlled trial |
title | Lung Ultrasound Guided Fluid Management Protocol for the Critically Ill Patient: study protocol for a multi-centre randomized controlled trial |
title_full | Lung Ultrasound Guided Fluid Management Protocol for the Critically Ill Patient: study protocol for a multi-centre randomized controlled trial |
title_fullStr | Lung Ultrasound Guided Fluid Management Protocol for the Critically Ill Patient: study protocol for a multi-centre randomized controlled trial |
title_full_unstemmed | Lung Ultrasound Guided Fluid Management Protocol for the Critically Ill Patient: study protocol for a multi-centre randomized controlled trial |
title_short | Lung Ultrasound Guided Fluid Management Protocol for the Critically Ill Patient: study protocol for a multi-centre randomized controlled trial |
title_sort | lung ultrasound guided fluid management protocol for the critically ill patient: study protocol for a multi-centre randomized controlled trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6482502/ https://www.ncbi.nlm.nih.gov/pubmed/31023358 http://dx.doi.org/10.1186/s13063-019-3345-0 |
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