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Molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit

BACKGROUND: Ventilator-associated pneumonia (VAP) is a known complication of mechanically ventilated children in the pediatric intensive care unit (PICU). Endotracheal tube (ETT) biofilms are often implicated in the development of VAP by providing a conduit for pathogens to the lower respiratory tra...

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Autores principales: Leroue, Matthew K., Harris, J. Kirk, Burgess, Katherine M., Stevens, Mark J., Miller, Joshua I., Sontag, Marci K., Sierra, Yamila L., Wagner, Brandie D., Mourani, Peter M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023549/
https://www.ncbi.nlm.nih.gov/pubmed/29963643
http://dx.doi.org/10.12715/apr.2017.4.14
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author Leroue, Matthew K.
Harris, J. Kirk
Burgess, Katherine M.
Stevens, Mark J.
Miller, Joshua I.
Sontag, Marci K.
Sierra, Yamila L.
Wagner, Brandie D.
Mourani, Peter M.
author_facet Leroue, Matthew K.
Harris, J. Kirk
Burgess, Katherine M.
Stevens, Mark J.
Miller, Joshua I.
Sontag, Marci K.
Sierra, Yamila L.
Wagner, Brandie D.
Mourani, Peter M.
author_sort Leroue, Matthew K.
collection PubMed
description BACKGROUND: Ventilator-associated pneumonia (VAP) is a known complication of mechanically ventilated children in the pediatric intensive care unit (PICU). Endotracheal tube (ETT) biofilms are often implicated in the development of VAP by providing a conduit for pathogens to the lower respiratory tract. METHODS: A prospective cohort study from April 2010–March 2011 of children 4 weeks to 18 years of age ventilated for greater than 72 hours to determine the microbiota of ETT biofilms and tracheal aspirates. RESULTS: Thirty-three patients were included with a mean age of 6.1 years (SD ± 5.1 years) and average length of intubation of 8.8 days (SD ± 5.0 days). Bacterial communities from tracheal aspirates and the proximal and distal ends of ETTs were determined using 16S rRNA gene libraries. Statistical analysis utilized two-part statistics and the Wilcoxon signed rank sum test for comparison of bacterial communities. Sequencing revealed a predominance of oropharyngeal microbiota including Prevotella and Streptococcus spp. Pathogenic bacterial genera including Staphylococcus, Burkholderia, Moraxella, and Haemophilus were also represented. Bacterial load was greatest at the proximal aspect of the ETT. Duration of intubation did not significantly impact bacterial load. Morisita Horn analysis across sites showed similar communities in 24/33 (72%) of patients. CONCLUSIONS: ETT biofilms and tracheal aspirates of intubated patients in the PICU primarily consisted of oropharyngeal microbiota, but had a significant representation of potentially pathogenic genera. While the majority of patients had similar microbiota when comparing their ETT biofilms and tracheal aspirates, a subset of patients showed a divergence between communities that requires further investigation.
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spelling pubmed-60235492018-06-28 Molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit Leroue, Matthew K. Harris, J. Kirk Burgess, Katherine M. Stevens, Mark J. Miller, Joshua I. Sontag, Marci K. Sierra, Yamila L. Wagner, Brandie D. Mourani, Peter M. Adv Pediatr Res Article BACKGROUND: Ventilator-associated pneumonia (VAP) is a known complication of mechanically ventilated children in the pediatric intensive care unit (PICU). Endotracheal tube (ETT) biofilms are often implicated in the development of VAP by providing a conduit for pathogens to the lower respiratory tract. METHODS: A prospective cohort study from April 2010–March 2011 of children 4 weeks to 18 years of age ventilated for greater than 72 hours to determine the microbiota of ETT biofilms and tracheal aspirates. RESULTS: Thirty-three patients were included with a mean age of 6.1 years (SD ± 5.1 years) and average length of intubation of 8.8 days (SD ± 5.0 days). Bacterial communities from tracheal aspirates and the proximal and distal ends of ETTs were determined using 16S rRNA gene libraries. Statistical analysis utilized two-part statistics and the Wilcoxon signed rank sum test for comparison of bacterial communities. Sequencing revealed a predominance of oropharyngeal microbiota including Prevotella and Streptococcus spp. Pathogenic bacterial genera including Staphylococcus, Burkholderia, Moraxella, and Haemophilus were also represented. Bacterial load was greatest at the proximal aspect of the ETT. Duration of intubation did not significantly impact bacterial load. Morisita Horn analysis across sites showed similar communities in 24/33 (72%) of patients. CONCLUSIONS: ETT biofilms and tracheal aspirates of intubated patients in the PICU primarily consisted of oropharyngeal microbiota, but had a significant representation of potentially pathogenic genera. While the majority of patients had similar microbiota when comparing their ETT biofilms and tracheal aspirates, a subset of patients showed a divergence between communities that requires further investigation. 2017-11-10 2017-12 /pmc/articles/PMC6023549/ /pubmed/29963643 http://dx.doi.org/10.12715/apr.2017.4.14 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Leroue, Matthew K.
Harris, J. Kirk
Burgess, Katherine M.
Stevens, Mark J.
Miller, Joshua I.
Sontag, Marci K.
Sierra, Yamila L.
Wagner, Brandie D.
Mourani, Peter M.
Molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit
title Molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit
title_full Molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit
title_fullStr Molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit
title_full_unstemmed Molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit
title_short Molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit
title_sort molecular analysis of endotracheal tube biofilms and tracheal aspirates in the pediatric intensive care unit
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6023549/
https://www.ncbi.nlm.nih.gov/pubmed/29963643
http://dx.doi.org/10.12715/apr.2017.4.14
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