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Characteristics and outcomes of patients with community-acquired and hospital-acquired sepsis
OBJECTIVE: To compare the clinical characteristics and outcomes of patients with community-acquired and hospital-acquired sepsis. METHODS: This is a retrospective cohort study that included all patients with a diagnosis of sepsis detected between January 2010 and December 2015 at a private hospital...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação de Medicina Intensiva Brasileira -
AMIB
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443308/ https://www.ncbi.nlm.nih.gov/pubmed/30970093 http://dx.doi.org/10.5935/0103-507X.20190013 |
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author | Westphal, Glauco Adrieno Pereira, Aline Braz Fachin, Silvia Maria Barreto, Ana Carolina Caldara Bornschein, Ana Carolina Gern Junqueira Caldeira Filho, Milton Koenig, Álvaro |
author_facet | Westphal, Glauco Adrieno Pereira, Aline Braz Fachin, Silvia Maria Barreto, Ana Carolina Caldara Bornschein, Ana Carolina Gern Junqueira Caldeira Filho, Milton Koenig, Álvaro |
author_sort | Westphal, Glauco Adrieno |
collection | PubMed |
description | OBJECTIVE: To compare the clinical characteristics and outcomes of patients with community-acquired and hospital-acquired sepsis. METHODS: This is a retrospective cohort study that included all patients with a diagnosis of sepsis detected between January 2010 and December 2015 at a private hospital in southern Brazil. Outcomes (mortality, intensive care unit and hospital lengths of stay) were measured by analyzing electronic records. RESULTS: There were 543 hospitalized patients with a diagnosis of sepsis, with a frequency of 90.5 (85 to 105) cases/year. Of these, 319 (58%) cases were classified as hospital-acquired sepsis. This group exhibited more severe disease and had a larger number of organ dysfunctions, with higher hospital [8 (8 - 10) versus 23 (20 - 27) days; p < 0.001] and intensive care unit [5 (4 - 7) versus 8.5 (7 - 10); p < 0.001] lengths of stay and higher in-hospital mortality (30.7% versus 15.6%; p < 0.001) than those with community-acquired sepsis. After adjusting for age, APACHE II scores, and hemodynamic and respiratory dysfunction, hospital-acquired sepsis remained associated with increased mortality (OR 1.96; 95%CI 1.15 - 3.32, p = 0.013). CONCLUSION: The present results contribute to the definition of the epidemiological profile of sepsis in the sample studied, in which hospital-acquired sepsis was more severe and was associated with higher mortality. |
format | Online Article Text |
id | pubmed-6443308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Associação de Medicina Intensiva Brasileira -
AMIB |
record_format | MEDLINE/PubMed |
spelling | pubmed-64433082019-04-04 Characteristics and outcomes of patients with community-acquired and hospital-acquired sepsis Westphal, Glauco Adrieno Pereira, Aline Braz Fachin, Silvia Maria Barreto, Ana Carolina Caldara Bornschein, Ana Carolina Gern Junqueira Caldeira Filho, Milton Koenig, Álvaro Rev Bras Ter Intensiva Original Articles OBJECTIVE: To compare the clinical characteristics and outcomes of patients with community-acquired and hospital-acquired sepsis. METHODS: This is a retrospective cohort study that included all patients with a diagnosis of sepsis detected between January 2010 and December 2015 at a private hospital in southern Brazil. Outcomes (mortality, intensive care unit and hospital lengths of stay) were measured by analyzing electronic records. RESULTS: There were 543 hospitalized patients with a diagnosis of sepsis, with a frequency of 90.5 (85 to 105) cases/year. Of these, 319 (58%) cases were classified as hospital-acquired sepsis. This group exhibited more severe disease and had a larger number of organ dysfunctions, with higher hospital [8 (8 - 10) versus 23 (20 - 27) days; p < 0.001] and intensive care unit [5 (4 - 7) versus 8.5 (7 - 10); p < 0.001] lengths of stay and higher in-hospital mortality (30.7% versus 15.6%; p < 0.001) than those with community-acquired sepsis. After adjusting for age, APACHE II scores, and hemodynamic and respiratory dysfunction, hospital-acquired sepsis remained associated with increased mortality (OR 1.96; 95%CI 1.15 - 3.32, p = 0.013). CONCLUSION: The present results contribute to the definition of the epidemiological profile of sepsis in the sample studied, in which hospital-acquired sepsis was more severe and was associated with higher mortality. Associação de Medicina Intensiva Brasileira - AMIB 2019 /pmc/articles/PMC6443308/ /pubmed/30970093 http://dx.doi.org/10.5935/0103-507X.20190013 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Westphal, Glauco Adrieno Pereira, Aline Braz Fachin, Silvia Maria Barreto, Ana Carolina Caldara Bornschein, Ana Carolina Gern Junqueira Caldeira Filho, Milton Koenig, Álvaro Characteristics and outcomes of patients with community-acquired and hospital-acquired sepsis |
title | Characteristics and outcomes of patients with community-acquired and
hospital-acquired sepsis |
title_full | Characteristics and outcomes of patients with community-acquired and
hospital-acquired sepsis |
title_fullStr | Characteristics and outcomes of patients with community-acquired and
hospital-acquired sepsis |
title_full_unstemmed | Characteristics and outcomes of patients with community-acquired and
hospital-acquired sepsis |
title_short | Characteristics and outcomes of patients with community-acquired and
hospital-acquired sepsis |
title_sort | characteristics and outcomes of patients with community-acquired and
hospital-acquired sepsis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443308/ https://www.ncbi.nlm.nih.gov/pubmed/30970093 http://dx.doi.org/10.5935/0103-507X.20190013 |
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