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Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients

BACKGROUND: Multiple organ dysfunction is a common cause of morbidity and mortality in intensive care units (ICUs). Original development of the Sequential Organ Failure Assessment (SOFA) score was not to predict outcome, but to describe temporal changes in organ dysfunction in critically ill patient...

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Autores principales: Soo, Andrea, Zuege, Danny J., Fick, Gordon H., Niven, Daniel J., Berthiaume, Luc R., Stelfox, Henry T., Doig, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533687/
https://www.ncbi.nlm.nih.gov/pubmed/31122276
http://dx.doi.org/10.1186/s13054-019-2459-9
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author Soo, Andrea
Zuege, Danny J.
Fick, Gordon H.
Niven, Daniel J.
Berthiaume, Luc R.
Stelfox, Henry T.
Doig, Christopher J.
author_facet Soo, Andrea
Zuege, Danny J.
Fick, Gordon H.
Niven, Daniel J.
Berthiaume, Luc R.
Stelfox, Henry T.
Doig, Christopher J.
author_sort Soo, Andrea
collection PubMed
description BACKGROUND: Multiple organ dysfunction is a common cause of morbidity and mortality in intensive care units (ICUs). Original development of the Sequential Organ Failure Assessment (SOFA) score was not to predict outcome, but to describe temporal changes in organ dysfunction in critically ill patients. Organ dysfunction scoring may be a reasonable surrogate outcome in clinical trials but further exploration of the impact of case mix on the temporal sequence of organ dysfunction is required. Our aim was to compare temporal changes in SOFA scores between hospital survivors and non-survivors. METHODS: We performed a population-based observational retrospective cohort study of critically ill patients admitted from January 1, 2004, to December 31, 2013, to 4 multisystem adult intensive care units (ICUs) in Calgary, Canada. The primary outcome was temporal changes in daily SOFA scores during the first 14 days of ICU admission. SOFA scores were modeled between hospital survivors and non-survivors using generalized estimating equations (GEE) and were also stratified by admission SOFA (≤ 11 versus > 11). RESULTS: The cohort consisted of 20,007 patients with at least one SOFA score and was mostly male (58.2%) with a median age of 59 (interquartile range [IQR] 44–72). Median ICU length of stay was 3.5 (IQR 1.7–7.5) days. ICU and hospital mortality were 18.5% and 25.5%, respectively. Temporal change in SOFA scores varied by survival and admission SOFA score in a complicated relationship. Area under the receiver operating characteristic (ROC) curve using admission SOFA as a predictor of hospital mortality was 0.77. The hospital mortality rate was 5.6% for patients with an admission SOFA of 0–2 and 94.4% with an admission SOFA of 20–24. There was an approximately linear increase in hospital mortality for SOFA scores of 3–19 (range 8.7–84.7%). CONCLUSIONS: Examining the clinical course of organ dysfunction in a large non-selective cohort of patients provides insight into the utility of SOFA. We have demonstrated that hospital outcome is associated with both admission SOFA and the temporal rate of change in SOFA after admission. It is necessary to further explore the impact of additional clinical factors on the clinical course of SOFA with large datasets. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2459-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-65336872019-05-29 Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients Soo, Andrea Zuege, Danny J. Fick, Gordon H. Niven, Daniel J. Berthiaume, Luc R. Stelfox, Henry T. Doig, Christopher J. Crit Care Research BACKGROUND: Multiple organ dysfunction is a common cause of morbidity and mortality in intensive care units (ICUs). Original development of the Sequential Organ Failure Assessment (SOFA) score was not to predict outcome, but to describe temporal changes in organ dysfunction in critically ill patients. Organ dysfunction scoring may be a reasonable surrogate outcome in clinical trials but further exploration of the impact of case mix on the temporal sequence of organ dysfunction is required. Our aim was to compare temporal changes in SOFA scores between hospital survivors and non-survivors. METHODS: We performed a population-based observational retrospective cohort study of critically ill patients admitted from January 1, 2004, to December 31, 2013, to 4 multisystem adult intensive care units (ICUs) in Calgary, Canada. The primary outcome was temporal changes in daily SOFA scores during the first 14 days of ICU admission. SOFA scores were modeled between hospital survivors and non-survivors using generalized estimating equations (GEE) and were also stratified by admission SOFA (≤ 11 versus > 11). RESULTS: The cohort consisted of 20,007 patients with at least one SOFA score and was mostly male (58.2%) with a median age of 59 (interquartile range [IQR] 44–72). Median ICU length of stay was 3.5 (IQR 1.7–7.5) days. ICU and hospital mortality were 18.5% and 25.5%, respectively. Temporal change in SOFA scores varied by survival and admission SOFA score in a complicated relationship. Area under the receiver operating characteristic (ROC) curve using admission SOFA as a predictor of hospital mortality was 0.77. The hospital mortality rate was 5.6% for patients with an admission SOFA of 0–2 and 94.4% with an admission SOFA of 20–24. There was an approximately linear increase in hospital mortality for SOFA scores of 3–19 (range 8.7–84.7%). CONCLUSIONS: Examining the clinical course of organ dysfunction in a large non-selective cohort of patients provides insight into the utility of SOFA. We have demonstrated that hospital outcome is associated with both admission SOFA and the temporal rate of change in SOFA after admission. It is necessary to further explore the impact of additional clinical factors on the clinical course of SOFA with large datasets. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2459-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-23 /pmc/articles/PMC6533687/ /pubmed/31122276 http://dx.doi.org/10.1186/s13054-019-2459-9 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 Research
Soo, Andrea
Zuege, Danny J.
Fick, Gordon H.
Niven, Daniel J.
Berthiaume, Luc R.
Stelfox, Henry T.
Doig, Christopher J.
Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients
title Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients
title_full Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients
title_fullStr Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients
title_full_unstemmed Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients
title_short Describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients
title_sort describing organ dysfunction in the intensive care unit: a cohort study of 20,000 patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6533687/
https://www.ncbi.nlm.nih.gov/pubmed/31122276
http://dx.doi.org/10.1186/s13054-019-2459-9
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