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Elucidating the role of procalcitonin as a biomarker in hospitalized COVID-19 patients
Our objectives were to evaluate the role of procalcitonin in identifying bacterial co-infections in hospitalized COVID-19 patients and quantify antibiotic prescribing during the 2020 pandemic surge. Hospitalized COVID-19 patients with both a procalcitonin test and blood or respiratory culture sent o...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065691/ https://www.ncbi.nlm.nih.gov/pubmed/35635888 http://dx.doi.org/10.1016/j.diagmicrobio.2022.115721 |
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author | Cowman, Kelsie Rossi, James Gendlina, Inessa Guo, Yi Liu, Sichen Szymczak, Wendy Forest, Stefanie K. Wolgast, Lucia Orner, Erika Bao, Hongkai Cervera-Hernandez, Miguel E. Ceniceros, Ashley Thota, Raja Pirofski, Liise-anne Nori, Priya |
author_facet | Cowman, Kelsie Rossi, James Gendlina, Inessa Guo, Yi Liu, Sichen Szymczak, Wendy Forest, Stefanie K. Wolgast, Lucia Orner, Erika Bao, Hongkai Cervera-Hernandez, Miguel E. Ceniceros, Ashley Thota, Raja Pirofski, Liise-anne Nori, Priya |
author_sort | Cowman, Kelsie |
collection | PubMed |
description | Our objectives were to evaluate the role of procalcitonin in identifying bacterial co-infections in hospitalized COVID-19 patients and quantify antibiotic prescribing during the 2020 pandemic surge. Hospitalized COVID-19 patients with both a procalcitonin test and blood or respiratory culture sent on admission were included in this retrospective study. Confirmed co-infection was determined by an infectious diseases specialist. In total, 819 patients were included; 335 (41%) had an elevated procalcitonin (>0.5 ng/mL) and of these, 42 (13%) had an initial bacterial co-infection. Positive predictive value of elevated procalcitonin for co-infection was 13% while the negative predictive value was 94%. Ninety-six percent of patients with an elevated procalcitonin received antibiotics (median 6 days of therapy), compared to 82% with low procalcitonin (median 4 days of therapy) (adjusted OR:3.3, P < 0.001). We observed elevated initial procalcitonin in many COVID patients without concurrent bacterial co-infections which potentially contributed to antibiotic over-prescribing. |
format | Online Article Text |
id | pubmed-9065691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90656912022-05-04 Elucidating the role of procalcitonin as a biomarker in hospitalized COVID-19 patients Cowman, Kelsie Rossi, James Gendlina, Inessa Guo, Yi Liu, Sichen Szymczak, Wendy Forest, Stefanie K. Wolgast, Lucia Orner, Erika Bao, Hongkai Cervera-Hernandez, Miguel E. Ceniceros, Ashley Thota, Raja Pirofski, Liise-anne Nori, Priya Diagn Microbiol Infect Dis Clinical Studies Our objectives were to evaluate the role of procalcitonin in identifying bacterial co-infections in hospitalized COVID-19 patients and quantify antibiotic prescribing during the 2020 pandemic surge. Hospitalized COVID-19 patients with both a procalcitonin test and blood or respiratory culture sent on admission were included in this retrospective study. Confirmed co-infection was determined by an infectious diseases specialist. In total, 819 patients were included; 335 (41%) had an elevated procalcitonin (>0.5 ng/mL) and of these, 42 (13%) had an initial bacterial co-infection. Positive predictive value of elevated procalcitonin for co-infection was 13% while the negative predictive value was 94%. Ninety-six percent of patients with an elevated procalcitonin received antibiotics (median 6 days of therapy), compared to 82% with low procalcitonin (median 4 days of therapy) (adjusted OR:3.3, P < 0.001). We observed elevated initial procalcitonin in many COVID patients without concurrent bacterial co-infections which potentially contributed to antibiotic over-prescribing. Elsevier Inc. 2022-08 2022-05-04 /pmc/articles/PMC9065691/ /pubmed/35635888 http://dx.doi.org/10.1016/j.diagmicrobio.2022.115721 Text en © 2022 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Clinical Studies Cowman, Kelsie Rossi, James Gendlina, Inessa Guo, Yi Liu, Sichen Szymczak, Wendy Forest, Stefanie K. Wolgast, Lucia Orner, Erika Bao, Hongkai Cervera-Hernandez, Miguel E. Ceniceros, Ashley Thota, Raja Pirofski, Liise-anne Nori, Priya Elucidating the role of procalcitonin as a biomarker in hospitalized COVID-19 patients |
title | Elucidating the role of procalcitonin as a biomarker in hospitalized COVID-19 patients |
title_full | Elucidating the role of procalcitonin as a biomarker in hospitalized COVID-19 patients |
title_fullStr | Elucidating the role of procalcitonin as a biomarker in hospitalized COVID-19 patients |
title_full_unstemmed | Elucidating the role of procalcitonin as a biomarker in hospitalized COVID-19 patients |
title_short | Elucidating the role of procalcitonin as a biomarker in hospitalized COVID-19 patients |
title_sort | elucidating the role of procalcitonin as a biomarker in hospitalized covid-19 patients |
topic | Clinical Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9065691/ https://www.ncbi.nlm.nih.gov/pubmed/35635888 http://dx.doi.org/10.1016/j.diagmicrobio.2022.115721 |
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