Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs

<p>Indigenous Australian children have high (up to 90%) rates of nasopharyngeal microbial colonisation and of hospitalisation for pneumonia. In Indigenous children hospitalised with pneumonia in Central Australia, we describe the nasopharyngeal detection of viruses and bacteria and assessed wh...

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Main Authors: Anne B Chang, Heidi Smith-Vaughan, Theo Sloots, Patricia C Valery, David Whiley, Jemima Beissbarth, Paul J Torzillo
Format: Article
Language:English
Published: BMC 2015-01-01
Series:Pneumonia
Subjects:
Online Access:https://pneumonia.org.au/index.php/pneumonia/article/view/636
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spelling doaj-d669a03c86724214a9690243757e1f6b2020-11-24T21:50:01ZengBMCPneumonia2200-61332015-01-0160485610.15172/pneu.2015.6/636517Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signsAnne B Chang0Heidi Smith-Vaughan1Theo Sloots2Patricia C Valery3David Whiley4Jemima Beissbarth5Paul J Torzillo6Menzies School of Health ResearchMenzies School of Health Research, Charles Darwin University, Casuarina, AustraliaQueensland Paediatric Infectious Diseases Laboratory, Sir Albert Sakzewksi Virus Research Centre, Queensland Children’s Health Services, Herston, Australia; Child Health Research Centre, The University of Queensland, Herston, AustraliaMenzies School of Health Research, Charles Darwin University, Casuarina, AustraliaQueensland Paediatric Infectious Diseases Laboratory, Sir Albert Sakzewksi Virus Research Centre, Queensland Children’s Health Services, Herston, Australia; Child Health Research Centre, The University of Queensland, Herston, AustraliaMenzies School of Health Research, Charles Darwin University, Casuarina, AustraliaSydney Medical School, University of Sydney, Sydney, Australia; Royal Prince Alfred Hospital, Sydney, Australia<p>Indigenous Australian children have high (up to 90%) rates of nasopharyngeal microbial colonisation and of hospitalisation for pneumonia. In Indigenous children hospitalised with pneumonia in Central Australia, we describe the nasopharyngeal detection of viruses and bacteria and assessed whether their presence related to signs of pneumonia (tachypnoea and/or chest in-drawing) on hospital admission and during subsequent days. Nasopharyngeal swabs (NPS) and data were prospectively collected from 145 children (median age = 23.5 months, interquartile range [IQR] 8.7–50) hospitalised with pneumonia at Alice Springs Hospital, Australia, between April 2001 and July 2002. The cohort was enrolled in a randomised controlled study using zinc and/or vitamin A supplementation. NPS were taken within 24 hours of hospitalisation and kept frozen at -80<sup>o</sup>C until analysed in 2014. Polymerase chain reaction (PCR) was used to detect <em>Moraxella catarrhalis</em>, <em>Haemophilus influenzae</em>, <em>Streptococcus pneumoniae</em>, <em>Staphylococcus aureus</em>, <em>Chlamydophila pneumoniae</em>, <em>Mycoplasma pneumoniae</em>, and 16 respiratory viruses. Uni- and multi-variate analyses were used to examine the relationships. One or more organisms were present in 137(94.5%) NPS; 133(91.7%) detected ³1 bacterium, 34(37.2%) for ³1 virus and 50(34.5%) were positive for both viruses and bacteria. <em>C. pneumoniae</em> (<em>n</em> = 3) and <em>M. pneumoniae</em> (<em>n</em> = 2) were rare. In multi-variate analyses, age &lt;12 months (odds ratio [OR] 6.6 [95% confidence interval {CI} 1.7–25.4]) and fever (OR 4.1 [95% CI 1.7–10.4]) were associated with tachypnoea and chest in-drawing. However the presence of bacteria and/or virus type was not associated with tachypnoea and/or chest in-drawing on admission or during recovery. In children with high nasopharyngeal microbial colonisation rates, the utility of NPS in determining the diagnosis of clinical pneumonia or duration of tachypnoea or in-drawing is likely limited. Larger cohort and case-control studies are required to confirm our findings.</p>https://pneumonia.org.au/index.php/pneumonia/article/view/636microbiology, pneumonia, radiology, Aboriginal, child, symptoms, hospitalised
collection DOAJ
language English
format Article
sources DOAJ
author Anne B Chang
Heidi Smith-Vaughan
Theo Sloots
Patricia C Valery
David Whiley
Jemima Beissbarth
Paul J Torzillo
spellingShingle Anne B Chang
Heidi Smith-Vaughan
Theo Sloots
Patricia C Valery
David Whiley
Jemima Beissbarth
Paul J Torzillo
Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs
Pneumonia
microbiology, pneumonia, radiology, Aboriginal, child, symptoms, hospitalised
author_facet Anne B Chang
Heidi Smith-Vaughan
Theo Sloots
Patricia C Valery
David Whiley
Jemima Beissbarth
Paul J Torzillo
author_sort Anne B Chang
title Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs
title_short Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs
title_full Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs
title_fullStr Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs
title_full_unstemmed Upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs
title_sort upper airway viruses and bacteria detection in clinical pneumonia in a population with high nasal colonisation do not relate to clinical signs
publisher BMC
series Pneumonia
issn 2200-6133
publishDate 2015-01-01
description <p>Indigenous Australian children have high (up to 90%) rates of nasopharyngeal microbial colonisation and of hospitalisation for pneumonia. In Indigenous children hospitalised with pneumonia in Central Australia, we describe the nasopharyngeal detection of viruses and bacteria and assessed whether their presence related to signs of pneumonia (tachypnoea and/or chest in-drawing) on hospital admission and during subsequent days. Nasopharyngeal swabs (NPS) and data were prospectively collected from 145 children (median age = 23.5 months, interquartile range [IQR] 8.7–50) hospitalised with pneumonia at Alice Springs Hospital, Australia, between April 2001 and July 2002. The cohort was enrolled in a randomised controlled study using zinc and/or vitamin A supplementation. NPS were taken within 24 hours of hospitalisation and kept frozen at -80<sup>o</sup>C until analysed in 2014. Polymerase chain reaction (PCR) was used to detect <em>Moraxella catarrhalis</em>, <em>Haemophilus influenzae</em>, <em>Streptococcus pneumoniae</em>, <em>Staphylococcus aureus</em>, <em>Chlamydophila pneumoniae</em>, <em>Mycoplasma pneumoniae</em>, and 16 respiratory viruses. Uni- and multi-variate analyses were used to examine the relationships. One or more organisms were present in 137(94.5%) NPS; 133(91.7%) detected ³1 bacterium, 34(37.2%) for ³1 virus and 50(34.5%) were positive for both viruses and bacteria. <em>C. pneumoniae</em> (<em>n</em> = 3) and <em>M. pneumoniae</em> (<em>n</em> = 2) were rare. In multi-variate analyses, age &lt;12 months (odds ratio [OR] 6.6 [95% confidence interval {CI} 1.7–25.4]) and fever (OR 4.1 [95% CI 1.7–10.4]) were associated with tachypnoea and chest in-drawing. However the presence of bacteria and/or virus type was not associated with tachypnoea and/or chest in-drawing on admission or during recovery. In children with high nasopharyngeal microbial colonisation rates, the utility of NPS in determining the diagnosis of clinical pneumonia or duration of tachypnoea or in-drawing is likely limited. Larger cohort and case-control studies are required to confirm our findings.</p>
topic microbiology, pneumonia, radiology, Aboriginal, child, symptoms, hospitalised
url https://pneumonia.org.au/index.php/pneumonia/article/view/636
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