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Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia
OBJECTIVES: SARS-CoV-2 may cause acute lung injury, and secondary infections are thus relevant complications in patients with COVID-19 pneumonia. However, detailed information on community- and hospital-acquired infections among patients with COVID-19 pneumonia is scarce. METHODS: We identified 220...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812551/ https://www.ncbi.nlm.nih.gov/pubmed/33461613 http://dx.doi.org/10.1186/s40560-021-00526-y |
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author | Søgaard, Kirstine K. Baettig, Veronika Osthoff, Michael Marsch, Stephan Leuzinger, Karoline Schweitzer, Michael Meier, Julian Bassetti, Stefano Bingisser, Roland Nickel, Christian H. Khanna, Nina Tschudin-Sutter, Sarah Weisser, Maja Battegay, Manuel Hirsch, Hans H. Pargger, Hans Siegemund, Martin Egli, Adrian |
author_facet | Søgaard, Kirstine K. Baettig, Veronika Osthoff, Michael Marsch, Stephan Leuzinger, Karoline Schweitzer, Michael Meier, Julian Bassetti, Stefano Bingisser, Roland Nickel, Christian H. Khanna, Nina Tschudin-Sutter, Sarah Weisser, Maja Battegay, Manuel Hirsch, Hans H. Pargger, Hans Siegemund, Martin Egli, Adrian |
author_sort | Søgaard, Kirstine K. |
collection | PubMed |
description | OBJECTIVES: SARS-CoV-2 may cause acute lung injury, and secondary infections are thus relevant complications in patients with COVID-19 pneumonia. However, detailed information on community- and hospital-acquired infections among patients with COVID-19 pneumonia is scarce. METHODS: We identified 220 SARS-CoV-2-positive patients hospitalized at the University Hospital Basel, Switzerland (between 25 February and 31 May 2020). We excluded patients who declined the general consent (n = 12), patients without clinical evidence of pneumonia (n = 29), and patients hospitalized for < 24 h (n = 17). We evaluated the frequency of community- and hospital-acquired infections using respiratory and blood culture materials with antigen, culture-based, and molecular diagnostics. For ICU patients, all clinical and microbial findings were re-evaluated interdisciplinary (intensive care, infectious disease, and clinical microbiology), and agreement reached to classify patients with infections. RESULTS: In the final cohort of 162 hospitalized patients (median age 64.4 years (IQR, 50.4–74.2); 61.1% male), 41 (25.3%) patients were admitted to the intensive care unit, 34/41 (82.9%) required mechanical ventilation, and 17 (10.5%) of all hospitalized patients died. In total, 31 infections were diagnosed including five viral co-infections, 24 bacterial infections, and three fungal infections (ventilator-associated pneumonia, n = 5; tracheobronchitis, n = 13; pneumonia, n = 1; and bloodstream infection, n = 6). Median time to respiratory tract infection was 12.5 days (IQR, 8–18) and time to bloodstream infection 14 days (IQR, 6–30). Hospital-acquired bacterial and fungal infections were more frequent among ICU patients than other patients (36.6% vs. 1.7%). Antibiotic or antifungal treatment was administered in 71 (43.8%) patients. CONCLUSIONS: Community-acquired viral and bacterial infections were rare among COVID-19 pneumonia patients. By contrast, hospital-acquired bacterial or fungal infections were frequently complicating the course among ICU patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40560-021-00526-y. |
format | Online Article Text |
id | pubmed-7812551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78125512021-01-18 Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia Søgaard, Kirstine K. Baettig, Veronika Osthoff, Michael Marsch, Stephan Leuzinger, Karoline Schweitzer, Michael Meier, Julian Bassetti, Stefano Bingisser, Roland Nickel, Christian H. Khanna, Nina Tschudin-Sutter, Sarah Weisser, Maja Battegay, Manuel Hirsch, Hans H. Pargger, Hans Siegemund, Martin Egli, Adrian J Intensive Care Research OBJECTIVES: SARS-CoV-2 may cause acute lung injury, and secondary infections are thus relevant complications in patients with COVID-19 pneumonia. However, detailed information on community- and hospital-acquired infections among patients with COVID-19 pneumonia is scarce. METHODS: We identified 220 SARS-CoV-2-positive patients hospitalized at the University Hospital Basel, Switzerland (between 25 February and 31 May 2020). We excluded patients who declined the general consent (n = 12), patients without clinical evidence of pneumonia (n = 29), and patients hospitalized for < 24 h (n = 17). We evaluated the frequency of community- and hospital-acquired infections using respiratory and blood culture materials with antigen, culture-based, and molecular diagnostics. For ICU patients, all clinical and microbial findings were re-evaluated interdisciplinary (intensive care, infectious disease, and clinical microbiology), and agreement reached to classify patients with infections. RESULTS: In the final cohort of 162 hospitalized patients (median age 64.4 years (IQR, 50.4–74.2); 61.1% male), 41 (25.3%) patients were admitted to the intensive care unit, 34/41 (82.9%) required mechanical ventilation, and 17 (10.5%) of all hospitalized patients died. In total, 31 infections were diagnosed including five viral co-infections, 24 bacterial infections, and three fungal infections (ventilator-associated pneumonia, n = 5; tracheobronchitis, n = 13; pneumonia, n = 1; and bloodstream infection, n = 6). Median time to respiratory tract infection was 12.5 days (IQR, 8–18) and time to bloodstream infection 14 days (IQR, 6–30). Hospital-acquired bacterial and fungal infections were more frequent among ICU patients than other patients (36.6% vs. 1.7%). Antibiotic or antifungal treatment was administered in 71 (43.8%) patients. CONCLUSIONS: Community-acquired viral and bacterial infections were rare among COVID-19 pneumonia patients. By contrast, hospital-acquired bacterial or fungal infections were frequently complicating the course among ICU patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40560-021-00526-y. BioMed Central 2021-01-18 /pmc/articles/PMC7812551/ /pubmed/33461613 http://dx.doi.org/10.1186/s40560-021-00526-y Text en © The Author(s) 2021 Open AccessThis 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/. 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 in a credit line to the data. |
spellingShingle | Research Søgaard, Kirstine K. Baettig, Veronika Osthoff, Michael Marsch, Stephan Leuzinger, Karoline Schweitzer, Michael Meier, Julian Bassetti, Stefano Bingisser, Roland Nickel, Christian H. Khanna, Nina Tschudin-Sutter, Sarah Weisser, Maja Battegay, Manuel Hirsch, Hans H. Pargger, Hans Siegemund, Martin Egli, Adrian Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia |
title | Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia |
title_full | Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia |
title_fullStr | Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia |
title_full_unstemmed | Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia |
title_short | Community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with COVID-19 pneumonia |
title_sort | community-acquired and hospital-acquired respiratory tract infection and bloodstream infection in patients hospitalized with covid-19 pneumonia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7812551/ https://www.ncbi.nlm.nih.gov/pubmed/33461613 http://dx.doi.org/10.1186/s40560-021-00526-y |
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