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The impact of comorbidities and COVID-19 on the evolution of community onset sepsis

Sepsis is a disease with high mortality and morbidity despite advances in diagnostic procedures and therapeutic strategies. The aim of this study was to evaluate the profile and outcomes of community-onset sepsis. This retrospective, multicenter study included five 24-h health care units and was con...

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Autores principales: de Araújo, Giovanna Colantuono, Pardini, Andrea, Lima, Camila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313672/
https://www.ncbi.nlm.nih.gov/pubmed/37391466
http://dx.doi.org/10.1038/s41598-023-37709-6
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author de Araújo, Giovanna Colantuono
Pardini, Andrea
Lima, Camila
author_facet de Araújo, Giovanna Colantuono
Pardini, Andrea
Lima, Camila
author_sort de Araújo, Giovanna Colantuono
collection PubMed
description Sepsis is a disease with high mortality and morbidity despite advances in diagnostic procedures and therapeutic strategies. The aim of this study was to evaluate the profile and outcomes of community-onset sepsis. This retrospective, multicenter study included five 24-h health care units and was conducted from January 2018 to December 2021. Patients were diagnosed with sepsis or septic shock according to the Sepsis 3.0 criterion. A total of 2630 patients diagnosed as having sepsis (68.4%, 1800) or septic shock (31.6%, 830) in the 24-h health care unit were included; 43.76% of the patients were admitted to the intensive care unit, 12.2% died, 4.1% had sepsis and 30% had septic shock. The comorbidities that were independent predictors of septic shock were chronic kidney disease on dialysis (CKD-d), bone marrow transplantation and neoplasia. CKD and neoplasia were also independent predictors of mortality, with ORs of 2.00 (CI 1.10–3.68) p = 0.023 and 1.74 (CI 1.319–2.298) p =  < 0.0001, respectively. Mortality according to the focus of primary infection was as follows: pulmonary 40.1%; COVID-19 35.7%; abdominal 8.1% and urinary 6.2%. Mortality due to the COVID-19 outbreak had an OR of 4.94 (CI 3.08–8.13) p ≤ 0.0001. Even though community-onset sepsis can be potentially fatal, this study revealed that some comorbidities lead to an increased risk of septic shock (d-CKD and neoplasia) and mortality. COVID-19 infection as the primary focus was an independent predictor of mortality in patients with sepsis when compared to other foci.
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spelling pubmed-103136722023-07-02 The impact of comorbidities and COVID-19 on the evolution of community onset sepsis de Araújo, Giovanna Colantuono Pardini, Andrea Lima, Camila Sci Rep Article Sepsis is a disease with high mortality and morbidity despite advances in diagnostic procedures and therapeutic strategies. The aim of this study was to evaluate the profile and outcomes of community-onset sepsis. This retrospective, multicenter study included five 24-h health care units and was conducted from January 2018 to December 2021. Patients were diagnosed with sepsis or septic shock according to the Sepsis 3.0 criterion. A total of 2630 patients diagnosed as having sepsis (68.4%, 1800) or septic shock (31.6%, 830) in the 24-h health care unit were included; 43.76% of the patients were admitted to the intensive care unit, 12.2% died, 4.1% had sepsis and 30% had septic shock. The comorbidities that were independent predictors of septic shock were chronic kidney disease on dialysis (CKD-d), bone marrow transplantation and neoplasia. CKD and neoplasia were also independent predictors of mortality, with ORs of 2.00 (CI 1.10–3.68) p = 0.023 and 1.74 (CI 1.319–2.298) p =  < 0.0001, respectively. Mortality according to the focus of primary infection was as follows: pulmonary 40.1%; COVID-19 35.7%; abdominal 8.1% and urinary 6.2%. Mortality due to the COVID-19 outbreak had an OR of 4.94 (CI 3.08–8.13) p ≤ 0.0001. Even though community-onset sepsis can be potentially fatal, this study revealed that some comorbidities lead to an increased risk of septic shock (d-CKD and neoplasia) and mortality. COVID-19 infection as the primary focus was an independent predictor of mortality in patients with sepsis when compared to other foci. Nature Publishing Group UK 2023-06-30 /pmc/articles/PMC10313672/ /pubmed/37391466 http://dx.doi.org/10.1038/s41598-023-37709-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
de Araújo, Giovanna Colantuono
Pardini, Andrea
Lima, Camila
The impact of comorbidities and COVID-19 on the evolution of community onset sepsis
title The impact of comorbidities and COVID-19 on the evolution of community onset sepsis
title_full The impact of comorbidities and COVID-19 on the evolution of community onset sepsis
title_fullStr The impact of comorbidities and COVID-19 on the evolution of community onset sepsis
title_full_unstemmed The impact of comorbidities and COVID-19 on the evolution of community onset sepsis
title_short The impact of comorbidities and COVID-19 on the evolution of community onset sepsis
title_sort impact of comorbidities and covid-19 on the evolution of community onset sepsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313672/
https://www.ncbi.nlm.nih.gov/pubmed/37391466
http://dx.doi.org/10.1038/s41598-023-37709-6
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