Your browser doesn't support javascript.
loading
Temporal airway microbiome changes related to ventilator-associated pneumonia in children.
Mourani, Peter M; Sontag, Marci K; Williamson, Kayla M; Harris, J Kirk; Reeder, Ron; Locandro, Chris; Carpenter, Todd C; Maddux, Aline B; Ziegler, Katherine; Simões, Eric A F; Osborne, Christina M; Ambroggio, Lilliam; Leroue, Matthew K; Robertson, Charles E; Langelier, Charles; DeRisi, Joseph L; Kamm, Jack; Hall, Mark W; Zuppa, Athena F; Carcillo, Joseph; Meert, Kathleen; Sapru, Anil; Pollack, Murray M; McQuillen, Patrick; Notterman, Daniel A; Dean, J Michael; Wagner, Brandie D.
Affiliation
  • Mourani PM; Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • Sontag MK; Epidemiology, University of Colorado, Colorado School of Public Health, Aurora, CO, USA.
  • Williamson KM; Biostatistics and Informatics, University of Colorado, Colorado School of Public Health, Aurora, CO, USA.
  • Harris JK; Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • Reeder R; Pediatrics, University of Utah, Salt Lake City, UT, USA.
  • Locandro C; Pediatrics, University of Utah, Salt Lake City, UT, USA.
  • Carpenter TC; Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • Maddux AB; Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • Ziegler K; Epidemiology, University of Colorado, Colorado School of Public Health, Aurora, CO, USA.
  • Simões EAF; Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • Osborne CM; Epidemiology, University of Colorado, Colorado School of Public Health, Aurora, CO, USA.
  • Ambroggio L; Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • Leroue MK; Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • Robertson CE; Epidemiology, University of Colorado, Colorado School of Public Health, Aurora, CO, USA.
  • Langelier C; Pediatrics, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • DeRisi JL; Medicine, Division of Infectious Diseases, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA.
  • Kamm J; Medicine, Division of Infectious Diseases, University of California San Francisco, San Francisco, CA, USA.
  • Hall MW; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Zuppa AF; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Carcillo J; Dept of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA, USA.
  • Meert K; Chan Zuckerberg Biohub, San Francisco, CA, USA.
  • Sapru A; Dept of Pediatrics, Nationwide Children's Hospital, Columbus, OH, USA.
  • Pollack MM; Anesthesiology and Critical Care Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • McQuillen P; Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
  • Notterman DA; Pediatrics, Children's Hospital of Michigan, Detroit, MI, USA.
  • Dean JM; Pediatrics, University of California Los Angeles, Los Angeles, CA, USA.
  • Wagner BD; Pediatrics, Children's National Medical Center and George Washington School of Medicine and Health Sciences, Washington, DC, USA.
Eur Respir J ; 57(3)2021 03.
Article in En | MEDLINE | ID: mdl-33008935
ABSTRACT
We sought to determine whether temporal changes in the lower airway microbiome are associated with ventilator-associated pneumonia (VAP) in children.Using a multicentre prospective study of children aged 31 days to 18 years requiring mechanical ventilation support for >72 h, daily tracheal aspirates were collected and analysed by sequencing of the 16S rRNA gene. VAP was assessed using 2008 Centers for Disease Control and Prevention paediatric criteria. The association between microbial factors and VAP was evaluated using joint longitudinal time-to-event modelling, matched case-control comparisons and unsupervised clustering.Out of 366 eligible subjects, 66 (15%) developed VAP at a median of 5 (interquartile range 3-5) days post intubation. At intubation, there was no difference in total bacterial load (TBL), but Shannon diversity and the relative abundance of Streptococcus, Lactobacillales and Prevotella were lower for VAP subjects versus non-VAP subjects. However, higher TBL on each sequential day was associated with a lower hazard (hazard ratio 0.39, 95% CI 0.23-0.64) for developing VAP, but sequential values of diversity were not associated with VAP. Similar findings were observed from the matched analysis and unsupervised clustering. The most common dominant VAP pathogens included Prevotella species (19%), Pseudomonas aeruginosa (14%) and Streptococcus mitis/pneumoniae (10%). Mycoplasma and Ureaplasma were also identified as dominant organisms in several subjects.In mechanically ventilated children, changes over time in microbial factors were marginally associated with VAP risk, although these changes were not suitable for predicting VAP in individual patients. These findings suggest that focusing exclusively on pathogen burden may not adequately inform VAP diagnosis.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia, Ventilator-Associated / Microbiota Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Eur Respir J Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia, Ventilator-Associated / Microbiota Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Child / Humans Language: En Journal: Eur Respir J Year: 2021 Type: Article Affiliation country: United States