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Bacterial coinfections with coronavirus disease 2019 (COVID-19)
BACKGROUND: The pandemic caused by severe acute respiratory coronavirus virus 2 (SARS-CoV-2) has dramatically increased cheshospitalizations, and it is often difficult to determine whether there is a bacterial or fungal coinfection at time of presentation. In this study, we sought to determine the r...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495532/ https://www.ncbi.nlm.nih.gov/pubmed/36168484 http://dx.doi.org/10.1017/ash.2021.187 |
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author | Huang, Glen Furukawa, Daisuke Yang, Bryant D. Kim, Brian J. Jeng, Arthur C. |
author_facet | Huang, Glen Furukawa, Daisuke Yang, Bryant D. Kim, Brian J. Jeng, Arthur C. |
author_sort | Huang, Glen |
collection | PubMed |
description | BACKGROUND: The pandemic caused by severe acute respiratory coronavirus virus 2 (SARS-CoV-2) has dramatically increased cheshospitalizations, and it is often difficult to determine whether there is a bacterial or fungal coinfection at time of presentation. In this study, we sought to determine the rates of coinfection and utilization of antibiotics in SARS-CoV-2 disease. METHODS: Retrospective chart review of patients hospitalized with COVID-19 pneumonia from April 13, 2020, to July 14, 2020. RESULTS: In total, 277 patients were hospitalized for COVID-19 pneumonia during this period. Patients that received antibiotics within 48 hours of presentation were more likely to be febrile (59.3% vs 41.2%; P = .01) and to have leukocytosis (23.9% vs 5.9%; P < .01) and were less likely to have a procalcitonin level <0.25 ng/mL (58.8% vs 74.5%; P = .04). In total, 45 patients had positive blood cultures collected during hospitalization, 16 of which were clinically significant. Of the clinically significant blood cultures, 5 were collected <48 hours of admission. Moreover, 18 sputum cultures were clinically significant, 2 of which were collected within 48 hours of admission. CONCLUSION: Bacterial and fungal coinfections in COVID-19 appear to be rare on presentation; thus, this factor may be a good target for enhanced antibiotic stewardship. |
format | Online Article Text |
id | pubmed-9495532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-94955322022-09-26 Bacterial coinfections with coronavirus disease 2019 (COVID-19) Huang, Glen Furukawa, Daisuke Yang, Bryant D. Kim, Brian J. Jeng, Arthur C. Antimicrob Steward Healthc Epidemiol Original Article BACKGROUND: The pandemic caused by severe acute respiratory coronavirus virus 2 (SARS-CoV-2) has dramatically increased cheshospitalizations, and it is often difficult to determine whether there is a bacterial or fungal coinfection at time of presentation. In this study, we sought to determine the rates of coinfection and utilization of antibiotics in SARS-CoV-2 disease. METHODS: Retrospective chart review of patients hospitalized with COVID-19 pneumonia from April 13, 2020, to July 14, 2020. RESULTS: In total, 277 patients were hospitalized for COVID-19 pneumonia during this period. Patients that received antibiotics within 48 hours of presentation were more likely to be febrile (59.3% vs 41.2%; P = .01) and to have leukocytosis (23.9% vs 5.9%; P < .01) and were less likely to have a procalcitonin level <0.25 ng/mL (58.8% vs 74.5%; P = .04). In total, 45 patients had positive blood cultures collected during hospitalization, 16 of which were clinically significant. Of the clinically significant blood cultures, 5 were collected <48 hours of admission. Moreover, 18 sputum cultures were clinically significant, 2 of which were collected within 48 hours of admission. CONCLUSION: Bacterial and fungal coinfections in COVID-19 appear to be rare on presentation; thus, this factor may be a good target for enhanced antibiotic stewardship. Cambridge University Press 2021-11-10 /pmc/articles/PMC9495532/ /pubmed/36168484 http://dx.doi.org/10.1017/ash.2021.187 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Huang, Glen Furukawa, Daisuke Yang, Bryant D. Kim, Brian J. Jeng, Arthur C. Bacterial coinfections with coronavirus disease 2019 (COVID-19) |
title | Bacterial coinfections with coronavirus disease 2019 (COVID-19) |
title_full | Bacterial coinfections with coronavirus disease 2019 (COVID-19) |
title_fullStr | Bacterial coinfections with coronavirus disease 2019 (COVID-19) |
title_full_unstemmed | Bacterial coinfections with coronavirus disease 2019 (COVID-19) |
title_short | Bacterial coinfections with coronavirus disease 2019 (COVID-19) |
title_sort | bacterial coinfections with coronavirus disease 2019 (covid-19) |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9495532/ https://www.ncbi.nlm.nih.gov/pubmed/36168484 http://dx.doi.org/10.1017/ash.2021.187 |
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