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The Impact of COVID-19 on the Profile of Hospital-Acquired Infections in Adult Intensive Care Units

Hospital-acquired infections (HAIs) are a global public health concern. As the COVID-19 pandemic continues, its contribution to mortality and antimicrobial resistance (AMR) grows, particularly in intensive care units (ICUs). A two-year retrospective study from April 2019–April 2021 was conducted in...

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Autores principales: Despotovic, Aleksa, Milosevic, Branko, Cirkovic, Andja, Vujovic, Ankica, Cucanic, Ksenija, Cucanic, Teodora, Stevanovic, Goran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8532680/
https://www.ncbi.nlm.nih.gov/pubmed/34680727
http://dx.doi.org/10.3390/antibiotics10101146
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author Despotovic, Aleksa
Milosevic, Branko
Cirkovic, Andja
Vujovic, Ankica
Cucanic, Ksenija
Cucanic, Teodora
Stevanovic, Goran
author_facet Despotovic, Aleksa
Milosevic, Branko
Cirkovic, Andja
Vujovic, Ankica
Cucanic, Ksenija
Cucanic, Teodora
Stevanovic, Goran
author_sort Despotovic, Aleksa
collection PubMed
description Hospital-acquired infections (HAIs) are a global public health concern. As the COVID-19 pandemic continues, its contribution to mortality and antimicrobial resistance (AMR) grows, particularly in intensive care units (ICUs). A two-year retrospective study from April 2019–April 2021 was conducted in an adult ICU at the Hospital for Infectious and Tropical Diseases, Belgrade, Serbia to assess causative agents of HAIs and AMR rates, with the COVID-19 pandemic ensuing halfway through the study. Resistance rates >80% were observed for the majority of tested antimicrobials. In COVID-19 patients, Acinetobacter spp. was the dominant cause of HAIs and more frequently isolated than in non-COVID-19 patients. (67 vs. 18, p = 0.001). Also, resistance was higher for imipenem (56.8% vs. 24.5%, p < 0.001), meropenem (61.1% vs. 24.3%, p < 0.001) and ciprofloxacin (59.5% vs. 36.9%, p = 0.04). AMR rates were aggregated with findings from our previous study to identify resistance trends and establish empiric treatment recommendations. The increased presence of Acinetobacter spp. and a positive trend in Klebsiella spp. resistance to fluoroquinolones (R(2) = 0.980, p = 0.01) and carbapenems (R(2) = 0.963, p = 0.02) could have contributed to alarming resistance rates across bloodstream infections (BSIs), pneumonia (PN), and urinary tract infections (UTIs). Exceptions were vancomycin (16.0%) and linezolid (2.6%) in BSIs; tigecycline (14.3%) and colistin (0%) in PNs; and colistin (12.0%) and linezolid (0%) in UTIs. COVID-19 has changed the landscape of HAIs in our ICUs. Approval of new drugs and rigorous surveillance is urgently needed.
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spelling pubmed-85326802021-10-23 The Impact of COVID-19 on the Profile of Hospital-Acquired Infections in Adult Intensive Care Units Despotovic, Aleksa Milosevic, Branko Cirkovic, Andja Vujovic, Ankica Cucanic, Ksenija Cucanic, Teodora Stevanovic, Goran Antibiotics (Basel) Article Hospital-acquired infections (HAIs) are a global public health concern. As the COVID-19 pandemic continues, its contribution to mortality and antimicrobial resistance (AMR) grows, particularly in intensive care units (ICUs). A two-year retrospective study from April 2019–April 2021 was conducted in an adult ICU at the Hospital for Infectious and Tropical Diseases, Belgrade, Serbia to assess causative agents of HAIs and AMR rates, with the COVID-19 pandemic ensuing halfway through the study. Resistance rates >80% were observed for the majority of tested antimicrobials. In COVID-19 patients, Acinetobacter spp. was the dominant cause of HAIs and more frequently isolated than in non-COVID-19 patients. (67 vs. 18, p = 0.001). Also, resistance was higher for imipenem (56.8% vs. 24.5%, p < 0.001), meropenem (61.1% vs. 24.3%, p < 0.001) and ciprofloxacin (59.5% vs. 36.9%, p = 0.04). AMR rates were aggregated with findings from our previous study to identify resistance trends and establish empiric treatment recommendations. The increased presence of Acinetobacter spp. and a positive trend in Klebsiella spp. resistance to fluoroquinolones (R(2) = 0.980, p = 0.01) and carbapenems (R(2) = 0.963, p = 0.02) could have contributed to alarming resistance rates across bloodstream infections (BSIs), pneumonia (PN), and urinary tract infections (UTIs). Exceptions were vancomycin (16.0%) and linezolid (2.6%) in BSIs; tigecycline (14.3%) and colistin (0%) in PNs; and colistin (12.0%) and linezolid (0%) in UTIs. COVID-19 has changed the landscape of HAIs in our ICUs. Approval of new drugs and rigorous surveillance is urgently needed. MDPI 2021-09-23 /pmc/articles/PMC8532680/ /pubmed/34680727 http://dx.doi.org/10.3390/antibiotics10101146 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Despotovic, Aleksa
Milosevic, Branko
Cirkovic, Andja
Vujovic, Ankica
Cucanic, Ksenija
Cucanic, Teodora
Stevanovic, Goran
The Impact of COVID-19 on the Profile of Hospital-Acquired Infections in Adult Intensive Care Units
title The Impact of COVID-19 on the Profile of Hospital-Acquired Infections in Adult Intensive Care Units
title_full The Impact of COVID-19 on the Profile of Hospital-Acquired Infections in Adult Intensive Care Units
title_fullStr The Impact of COVID-19 on the Profile of Hospital-Acquired Infections in Adult Intensive Care Units
title_full_unstemmed The Impact of COVID-19 on the Profile of Hospital-Acquired Infections in Adult Intensive Care Units
title_short The Impact of COVID-19 on the Profile of Hospital-Acquired Infections in Adult Intensive Care Units
title_sort impact of covid-19 on the profile of hospital-acquired infections in adult intensive care units
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8532680/
https://www.ncbi.nlm.nih.gov/pubmed/34680727
http://dx.doi.org/10.3390/antibiotics10101146
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