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Nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia
BACKGROUND/AIMS: The relationship between nonpulmonary organ failure and the development of acute respiratory distress syndrome (ARDS) in patients with sepsis has not been well studied. METHODS: We retrospectively reviewed the medical records of patients with septic bacteremia admitted to the medica...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Association of Internal Medicine
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325442/ https://www.ncbi.nlm.nih.gov/pubmed/29898577 http://dx.doi.org/10.3904/kjim.2017.204 |
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author | Nam, Hyunseung Jang, Seung Hun Hwang, Yong Il Kim, Joo-Hee Park, Ji Young Park, Sunghoon |
author_facet | Nam, Hyunseung Jang, Seung Hun Hwang, Yong Il Kim, Joo-Hee Park, Ji Young Park, Sunghoon |
author_sort | Nam, Hyunseung |
collection | PubMed |
description | BACKGROUND/AIMS: The relationship between nonpulmonary organ failure and the development of acute respiratory distress syndrome (ARDS) in patients with sepsis has not been well studied. METHODS: We retrospectively reviewed the medical records of patients with septic bacteremia admitted to the medical intensive care unit (ICU) of a tertiary academic hospital between January 2013 and December 2016. RESULTS: The study enrolled 125 patients of median age 73.0 years. Urinary (n = 47), hepatobiliary (n = 30), and pulmonary infections (n = 28) were the most common causes of sepsis; the incidence of ARDS was 17.6%. The total number of nonpulmonary organ failures at the time of ICU admission was higher in patients with ARDS than in those without (p = 0.011), and the cardiovascular, central nervous system (CNS), and coagulation scores were significantly higher in ARDS patients. On multivariate analysis, apart from pneumonia sepsis, the CNS (odds ratio [OR], 1.917; 95% confidence interval [CI], 1.097 to 3.348) and coagulation scores (OR, 2.669; 95% CI, 1.438 to 4.954) were significantly associated with ARDS development. The 28-day and in-hospital mortality rates were higher in those with ARDS than in those without (63.6 vs. 8.7%, p < 0.001; 72.7% vs. 11.7%, p < 0.001), and ARDS development was found to be an independent risk factor for 28-day mortality. CONCLUSIONS: Apart from pneumonia, CNS dysfunction and coagulopathy were significantly associated with ARDS development, which was an independent risk factor for 28-day mortality. |
format | Online Article Text |
id | pubmed-6325442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Korean Association of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-63254422019-01-11 Nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia Nam, Hyunseung Jang, Seung Hun Hwang, Yong Il Kim, Joo-Hee Park, Ji Young Park, Sunghoon Korean J Intern Med Original Article BACKGROUND/AIMS: The relationship between nonpulmonary organ failure and the development of acute respiratory distress syndrome (ARDS) in patients with sepsis has not been well studied. METHODS: We retrospectively reviewed the medical records of patients with septic bacteremia admitted to the medical intensive care unit (ICU) of a tertiary academic hospital between January 2013 and December 2016. RESULTS: The study enrolled 125 patients of median age 73.0 years. Urinary (n = 47), hepatobiliary (n = 30), and pulmonary infections (n = 28) were the most common causes of sepsis; the incidence of ARDS was 17.6%. The total number of nonpulmonary organ failures at the time of ICU admission was higher in patients with ARDS than in those without (p = 0.011), and the cardiovascular, central nervous system (CNS), and coagulation scores were significantly higher in ARDS patients. On multivariate analysis, apart from pneumonia sepsis, the CNS (odds ratio [OR], 1.917; 95% confidence interval [CI], 1.097 to 3.348) and coagulation scores (OR, 2.669; 95% CI, 1.438 to 4.954) were significantly associated with ARDS development. The 28-day and in-hospital mortality rates were higher in those with ARDS than in those without (63.6 vs. 8.7%, p < 0.001; 72.7% vs. 11.7%, p < 0.001), and ARDS development was found to be an independent risk factor for 28-day mortality. CONCLUSIONS: Apart from pneumonia, CNS dysfunction and coagulopathy were significantly associated with ARDS development, which was an independent risk factor for 28-day mortality. The Korean Association of Internal Medicine 2019-01 2018-06-14 /pmc/articles/PMC6325442/ /pubmed/29898577 http://dx.doi.org/10.3904/kjim.2017.204 Text en Copyright © 2019 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nam, Hyunseung Jang, Seung Hun Hwang, Yong Il Kim, Joo-Hee Park, Ji Young Park, Sunghoon Nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia |
title | Nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia |
title_full | Nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia |
title_fullStr | Nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia |
title_full_unstemmed | Nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia |
title_short | Nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia |
title_sort | nonpulmonary risk factors of acute respiratory distress syndrome in patients with septic bacteraemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325442/ https://www.ncbi.nlm.nih.gov/pubmed/29898577 http://dx.doi.org/10.3904/kjim.2017.204 |
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