Procalcitonin Increase Is Associated with the Development of Critical Care-Acquired Infections in COVID-19 ARDS
Secondary bacterial infection in COVID-19 patients is associated with increased mortality and disproportionately affects critically ill patients. This single-centre retrospective observational study investigates the comparative efficacy of change in procalcitonin (PCT) and other commonly available b...
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2021
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oai:doaj.org-article:81e29d712ba44af68bce49b9540bcb3f2021-11-25T16:25:13ZProcalcitonin Increase Is Associated with the Development of Critical Care-Acquired Infections in COVID-19 ARDS10.3390/antibiotics101114252079-6382https://doaj.org/article/81e29d712ba44af68bce49b9540bcb3f2021-11-01T00:00:00Zhttps://www.mdpi.com/2079-6382/10/11/1425https://doaj.org/toc/2079-6382Secondary bacterial infection in COVID-19 patients is associated with increased mortality and disproportionately affects critically ill patients. This single-centre retrospective observational study investigates the comparative efficacy of change in procalcitonin (PCT) and other commonly available biomarkers in revealing or predicting microbiologically proven secondary infection in critical COVID-19 patients. Adult patients admitted to an intensive care unit (ICU) with confirmed SARS-CoV-2 infection between 9 March 2020 and 5 June 2020 were recruited to the study. For daily biomarker and secondary infection, laboratory-confirmed bloodstream infection (LCBI) and ventilator-associated pneumonia/tracheobronchitis (VAP/VAT) data were collected. We observed a PCT rise in 53 (81.5%) of the patients, a C-reactive protein (CRP) rise in 55 (84.6%) and a white blood cell count (WBC) rise in 61 (93.8%). Secondary infection was confirmed in 33 (50.8%) of the patients. A PCT rise was present in 97.0% of patients with at least one confirmed VAP/VAT and/or LCBI event. CRP and WBC rises occurred in 93.9% and 97.0% of patients with confirmed VAP/VAT and/or LCBI, respectively. Logistic regression analysis found that, when including all biomarkers in the same model, there was a significant association between PCT rise and the occurrence of LCBI and/or VAP/VAT (OR = 14.86 95%CI: 2.20, 342.53; <i>p</i> = 0.021). Conversely, no statistically significant relationship was found between either a CRP rise (<i>p</i> = 0.167) or a WBC rise (<i>p</i> = 0.855) and the occurrence of VAP/VAT and/or LCBI. These findings provide a promising insight into the usefulness of PCT measurement in predicting the emergence of secondary bacterial infection in ICU.Owen RichardsPhilip PallmannCharles KingYusuf CheemaCharlotte KillickEmma Thomas-JonesJessica HarrisCatherine BaileyTamas SzakmanyMDPI AGarticleCOVID-19procalcitoninC-reactive proteinsecondary infectionTherapeutics. PharmacologyRM1-950ENAntibiotics, Vol 10, Iss 1425, p 1425 (2021) |
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COVID-19 procalcitonin C-reactive protein secondary infection Therapeutics. Pharmacology RM1-950 |
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COVID-19 procalcitonin C-reactive protein secondary infection Therapeutics. Pharmacology RM1-950 Owen Richards Philip Pallmann Charles King Yusuf Cheema Charlotte Killick Emma Thomas-Jones Jessica Harris Catherine Bailey Tamas Szakmany Procalcitonin Increase Is Associated with the Development of Critical Care-Acquired Infections in COVID-19 ARDS |
description |
Secondary bacterial infection in COVID-19 patients is associated with increased mortality and disproportionately affects critically ill patients. This single-centre retrospective observational study investigates the comparative efficacy of change in procalcitonin (PCT) and other commonly available biomarkers in revealing or predicting microbiologically proven secondary infection in critical COVID-19 patients. Adult patients admitted to an intensive care unit (ICU) with confirmed SARS-CoV-2 infection between 9 March 2020 and 5 June 2020 were recruited to the study. For daily biomarker and secondary infection, laboratory-confirmed bloodstream infection (LCBI) and ventilator-associated pneumonia/tracheobronchitis (VAP/VAT) data were collected. We observed a PCT rise in 53 (81.5%) of the patients, a C-reactive protein (CRP) rise in 55 (84.6%) and a white blood cell count (WBC) rise in 61 (93.8%). Secondary infection was confirmed in 33 (50.8%) of the patients. A PCT rise was present in 97.0% of patients with at least one confirmed VAP/VAT and/or LCBI event. CRP and WBC rises occurred in 93.9% and 97.0% of patients with confirmed VAP/VAT and/or LCBI, respectively. Logistic regression analysis found that, when including all biomarkers in the same model, there was a significant association between PCT rise and the occurrence of LCBI and/or VAP/VAT (OR = 14.86 95%CI: 2.20, 342.53; <i>p</i> = 0.021). Conversely, no statistically significant relationship was found between either a CRP rise (<i>p</i> = 0.167) or a WBC rise (<i>p</i> = 0.855) and the occurrence of VAP/VAT and/or LCBI. These findings provide a promising insight into the usefulness of PCT measurement in predicting the emergence of secondary bacterial infection in ICU. |
format |
article |
author |
Owen Richards Philip Pallmann Charles King Yusuf Cheema Charlotte Killick Emma Thomas-Jones Jessica Harris Catherine Bailey Tamas Szakmany |
author_facet |
Owen Richards Philip Pallmann Charles King Yusuf Cheema Charlotte Killick Emma Thomas-Jones Jessica Harris Catherine Bailey Tamas Szakmany |
author_sort |
Owen Richards |
title |
Procalcitonin Increase Is Associated with the Development of Critical Care-Acquired Infections in COVID-19 ARDS |
title_short |
Procalcitonin Increase Is Associated with the Development of Critical Care-Acquired Infections in COVID-19 ARDS |
title_full |
Procalcitonin Increase Is Associated with the Development of Critical Care-Acquired Infections in COVID-19 ARDS |
title_fullStr |
Procalcitonin Increase Is Associated with the Development of Critical Care-Acquired Infections in COVID-19 ARDS |
title_full_unstemmed |
Procalcitonin Increase Is Associated with the Development of Critical Care-Acquired Infections in COVID-19 ARDS |
title_sort |
procalcitonin increase is associated with the development of critical care-acquired infections in covid-19 ards |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/81e29d712ba44af68bce49b9540bcb3f |
work_keys_str_mv |
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