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Healthcare-associated bacterial infections in the paediatric ICU
BACKGROUND: An estimated 3.2 million patients annually develop healthcare-associated infections (HCAIs) in Europe alone amid the major challenge of increasing antimicrobial resistance. Critically ill children warrant specific evaluation because of differences in epidemiology, causative organisms and...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210264/ https://www.ncbi.nlm.nih.gov/pubmed/34223023 http://dx.doi.org/10.1093/jacamr/dlaa066 |
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author | Akinkugbe, Olugbenga Cooke, Fiona J Pathan, Nazima |
author_facet | Akinkugbe, Olugbenga Cooke, Fiona J Pathan, Nazima |
author_sort | Akinkugbe, Olugbenga |
collection | PubMed |
description | BACKGROUND: An estimated 3.2 million patients annually develop healthcare-associated infections (HCAIs) in Europe alone amid the major challenge of increasing antimicrobial resistance. Critically ill children warrant specific evaluation because of differences in epidemiology, causative organisms and infection sites. OBJECTIVES: To examine the prevalence and antimicrobial susceptibility patterns of three types of HCAI in critically ill children and determine the effect on their disease course. MATERIALS AND METHODS: Retrospective cohort review of critically ill children admitted to a general paediatric ICU (PICU) at a regional academic tertiary referral centre over a 3 year period. RESULTS: There were 1930 admissions with a median age of 38 months. Children with HCAIs had a higher incidence of comorbidities (74% versus 24%) and a longer median length of stay (8 days versus 3 days). We identified 26 positive isolates (blood, lower respiratory and urine) taken 48 h or more after admission. The combined incidence was 1.34%. Hospital-acquired pneumonia accounted for 58% of HCAIs, urinary tract infections for 31% and bloodstream infections for 11%. The majority (61.5%) of HCAIs were caused by Gram-negative organisms. Seven isolates were resistant to antimicrobials used to treat HCAI. All of these were Gram-negative organisms (Pseudomonas aeruginosa, Klebsiella oxytoca and Escherichia coli). CONCLUSIONS: These data revealed a low incidence of HCAIs, 27% of which were resistant Gram-negative organisms. Critically ill children with HCAIs were more likely to have comorbidities and an increased length of stay. These factors may increasingly impact on PICU bed availability, an already limited resource. |
format | Online Article Text |
id | pubmed-8210264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82102642021-07-02 Healthcare-associated bacterial infections in the paediatric ICU Akinkugbe, Olugbenga Cooke, Fiona J Pathan, Nazima JAC Antimicrob Resist Original Article BACKGROUND: An estimated 3.2 million patients annually develop healthcare-associated infections (HCAIs) in Europe alone amid the major challenge of increasing antimicrobial resistance. Critically ill children warrant specific evaluation because of differences in epidemiology, causative organisms and infection sites. OBJECTIVES: To examine the prevalence and antimicrobial susceptibility patterns of three types of HCAI in critically ill children and determine the effect on their disease course. MATERIALS AND METHODS: Retrospective cohort review of critically ill children admitted to a general paediatric ICU (PICU) at a regional academic tertiary referral centre over a 3 year period. RESULTS: There were 1930 admissions with a median age of 38 months. Children with HCAIs had a higher incidence of comorbidities (74% versus 24%) and a longer median length of stay (8 days versus 3 days). We identified 26 positive isolates (blood, lower respiratory and urine) taken 48 h or more after admission. The combined incidence was 1.34%. Hospital-acquired pneumonia accounted for 58% of HCAIs, urinary tract infections for 31% and bloodstream infections for 11%. The majority (61.5%) of HCAIs were caused by Gram-negative organisms. Seven isolates were resistant to antimicrobials used to treat HCAI. All of these were Gram-negative organisms (Pseudomonas aeruginosa, Klebsiella oxytoca and Escherichia coli). CONCLUSIONS: These data revealed a low incidence of HCAIs, 27% of which were resistant Gram-negative organisms. Critically ill children with HCAIs were more likely to have comorbidities and an increased length of stay. These factors may increasingly impact on PICU bed availability, an already limited resource. Oxford University Press 2020-09-14 /pmc/articles/PMC8210264/ /pubmed/34223023 http://dx.doi.org/10.1093/jacamr/dlaa066 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Akinkugbe, Olugbenga Cooke, Fiona J Pathan, Nazima Healthcare-associated bacterial infections in the paediatric ICU |
title | Healthcare-associated bacterial infections in the paediatric ICU |
title_full | Healthcare-associated bacterial infections in the paediatric ICU |
title_fullStr | Healthcare-associated bacterial infections in the paediatric ICU |
title_full_unstemmed | Healthcare-associated bacterial infections in the paediatric ICU |
title_short | Healthcare-associated bacterial infections in the paediatric ICU |
title_sort | healthcare-associated bacterial infections in the paediatric icu |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8210264/ https://www.ncbi.nlm.nih.gov/pubmed/34223023 http://dx.doi.org/10.1093/jacamr/dlaa066 |
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