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Early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients

BACKGROUND: Sepsis is a major risk factor for acute respiratory distress syndrome (ARDS). However, there remains a paucity of literature examining risk factors for ARDS in septic patients early in their course. This study examined the role of early fluid administration and identified other risk fact...

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Autores principales: Seethala, Raghu R., Hou, Peter C., Aisiku, Imoigele P., Frendl, Gyorgy, Park, Pauline K., Mikkelsen, Mark E., Chang, Steven Y., Gajic, Ognjen, Sevransky, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Paris 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256622/
https://www.ncbi.nlm.nih.gov/pubmed/28116595
http://dx.doi.org/10.1186/s13613-017-0233-1
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author Seethala, Raghu R.
Hou, Peter C.
Aisiku, Imoigele P.
Frendl, Gyorgy
Park, Pauline K.
Mikkelsen, Mark E.
Chang, Steven Y.
Gajic, Ognjen
Sevransky, Jonathan
author_facet Seethala, Raghu R.
Hou, Peter C.
Aisiku, Imoigele P.
Frendl, Gyorgy
Park, Pauline K.
Mikkelsen, Mark E.
Chang, Steven Y.
Gajic, Ognjen
Sevransky, Jonathan
author_sort Seethala, Raghu R.
collection PubMed
description BACKGROUND: Sepsis is a major risk factor for acute respiratory distress syndrome (ARDS). However, there remains a paucity of literature examining risk factors for ARDS in septic patients early in their course. This study examined the role of early fluid administration and identified other risk factors within the first 6 h of hospital presentation associated with developing ARDS in septic patients. METHODS: This was a secondary analysis of septic adult patients presenting to the Emergency Department or being admitted for high-risk elective surgery from the multicenter observational cohort study, US Critical Injury and Illness trial Group-Lung Injury Prevention Study 1 (USCIITG-LIPS 1, NCT00889772). Multivariable logistic regression was performed to identify potential early risk factors for ARDS. Stratified analysis by shock status was performed to examine the association between early fluid administration and ARDS. RESULTS: Of the 5584 patients in the original study cohort, 2534 (45.4%) met our criteria for sepsis. One hundred and fifty-six (6.2%) of these patients developed ARDS during the hospital stay. In multivariable analyses, Acute Physiology and Chronic Health Evaluation (APACHE) II score (OR 1.10, 95% CI 1.07–1.13), age (OR 0.97, 95% CI 0.96–0.98), total fluid infused in the first 6 h (in liters) (OR 1.15, 95% CI 1.03–1.29), shock (OR 2.57, 95% CI 1.62–4.08), pneumonia as a site of infection (OR 2.31, 95% CI 1.59–3.36), pancreatitis (OR 3.86, 95% CI 1.33–11.24), and acute abdomen (OR 3.77, 95% CI 1.37–10.41) were associated with developing ARDS. In the stratified analysis, total fluid infused in the first 6 h (in liters) (OR 1.05, 95% CI 0.87–1.28) was not associated with the development of ARDS in the shock group, while there was an association in the non-shock group (OR 1.21, 95% CI 1.05–1.38). CONCLUSIONS: In septic patients, the following risk factors identified within the first 6 h of hospital presentation were associated with ARDS: APACHE II score, presence of shock, pulmonary source of infection, pancreatitis, and presence of an acute abdomen. In septic patients without shock, the amount of fluid infused during the first 6 h of hospital presentation was associated with developing ARDS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13613-017-0233-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-52566222017-01-25 Early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients Seethala, Raghu R. Hou, Peter C. Aisiku, Imoigele P. Frendl, Gyorgy Park, Pauline K. Mikkelsen, Mark E. Chang, Steven Y. Gajic, Ognjen Sevransky, Jonathan Ann Intensive Care Research BACKGROUND: Sepsis is a major risk factor for acute respiratory distress syndrome (ARDS). However, there remains a paucity of literature examining risk factors for ARDS in septic patients early in their course. This study examined the role of early fluid administration and identified other risk factors within the first 6 h of hospital presentation associated with developing ARDS in septic patients. METHODS: This was a secondary analysis of septic adult patients presenting to the Emergency Department or being admitted for high-risk elective surgery from the multicenter observational cohort study, US Critical Injury and Illness trial Group-Lung Injury Prevention Study 1 (USCIITG-LIPS 1, NCT00889772). Multivariable logistic regression was performed to identify potential early risk factors for ARDS. Stratified analysis by shock status was performed to examine the association between early fluid administration and ARDS. RESULTS: Of the 5584 patients in the original study cohort, 2534 (45.4%) met our criteria for sepsis. One hundred and fifty-six (6.2%) of these patients developed ARDS during the hospital stay. In multivariable analyses, Acute Physiology and Chronic Health Evaluation (APACHE) II score (OR 1.10, 95% CI 1.07–1.13), age (OR 0.97, 95% CI 0.96–0.98), total fluid infused in the first 6 h (in liters) (OR 1.15, 95% CI 1.03–1.29), shock (OR 2.57, 95% CI 1.62–4.08), pneumonia as a site of infection (OR 2.31, 95% CI 1.59–3.36), pancreatitis (OR 3.86, 95% CI 1.33–11.24), and acute abdomen (OR 3.77, 95% CI 1.37–10.41) were associated with developing ARDS. In the stratified analysis, total fluid infused in the first 6 h (in liters) (OR 1.05, 95% CI 0.87–1.28) was not associated with the development of ARDS in the shock group, while there was an association in the non-shock group (OR 1.21, 95% CI 1.05–1.38). CONCLUSIONS: In septic patients, the following risk factors identified within the first 6 h of hospital presentation were associated with ARDS: APACHE II score, presence of shock, pulmonary source of infection, pancreatitis, and presence of an acute abdomen. In septic patients without shock, the amount of fluid infused during the first 6 h of hospital presentation was associated with developing ARDS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13613-017-0233-1) contains supplementary material, which is available to authorized users. Springer Paris 2017-01-23 /pmc/articles/PMC5256622/ /pubmed/28116595 http://dx.doi.org/10.1186/s13613-017-0233-1 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.
spellingShingle Research
Seethala, Raghu R.
Hou, Peter C.
Aisiku, Imoigele P.
Frendl, Gyorgy
Park, Pauline K.
Mikkelsen, Mark E.
Chang, Steven Y.
Gajic, Ognjen
Sevransky, Jonathan
Early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients
title Early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients
title_full Early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients
title_fullStr Early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients
title_full_unstemmed Early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients
title_short Early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients
title_sort early risk factors and the role of fluid administration in developing acute respiratory distress syndrome in septic patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256622/
https://www.ncbi.nlm.nih.gov/pubmed/28116595
http://dx.doi.org/10.1186/s13613-017-0233-1
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