Association between early bacterial carriage and otitis media in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia: a cohort study

<p>Abstract</p> <p>Background</p> <p><it>Streptococcus pneumoniae</it> (Pnc), nontypeable <it>Haemophilus influenzae</it> (NTHi) and <it>Moraxella catarrhalis</it> (Mcat) are the most important bacterial pathogens associated with otit...

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Main Authors: Sun Wenxing, Jacoby Peter, Riley Thomas V, Bowman Jacinta, Leach Amanda Jane, Coates Harvey, Weeks Sharon, Cripps Allan, Lehmann Deborah
Format: Article
Language:English
Published: BMC 2012-12-01
Series:BMC Infectious Diseases
Subjects:
Online Access:http://www.biomedcentral.com/1471-2334/12/366
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spelling doaj-2831cfd078c243e7b38503db96b6b5482020-11-25T02:58:05ZengBMCBMC Infectious Diseases1471-23342012-12-0112136610.1186/1471-2334-12-366Association between early bacterial carriage and otitis media in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia: a cohort studySun WenxingJacoby PeterRiley Thomas VBowman JacintaLeach Amanda JaneCoates HarveyWeeks SharonCripps AllanLehmann Deborah<p>Abstract</p> <p>Background</p> <p><it>Streptococcus pneumoniae</it> (Pnc), nontypeable <it>Haemophilus influenzae</it> (NTHi) and <it>Moraxella catarrhalis</it> (Mcat) are the most important bacterial pathogens associated with otitis media (OM). Previous studies have suggested that early upper respiratory tract (URT) bacterial carriage may increase risk of subsequent OM. We investigated associations between early onset of URT bacterial carriage and subsequent diagnosis of OM in Aboriginal and non-Aboriginal children living in the Kalgoorlie-Boulder region located in a semi-arid zone of Western Australia.</p> <p>Methods</p> <p>Aboriginal and non-Aboriginal children who had nasopharyngeal aspirates collected at age 1- < 3 months and at least one clinical examination for OM by an ear, nose and throat specialist before age 2 years were included in this analysis. Tympanometry to detect middle ear effusion was also performed at 2- to 6-monthly scheduled field visits from age 3 months. Multivariate regression models were used to investigate the relationship between early carriage and subsequent diagnosis of OM controlling for environmental factors.</p> <p>Results</p> <p>Carriage rates of Pnc, NTHi and Mcat at age 1- < 3 months were 45%, 29% and 48%, respectively, in 66 Aboriginal children and 14%, 5% and 18% in 146 non-Aboriginal children. OM was diagnosed at least once in 71% of Aboriginal children and 43% of non-Aboriginal children. After controlling for age, sex, presence of other bacteria and environmental factors, early nasopharyngeal carriage of NTHi increased the risk of subsequent OM (odds ratio = 3.70, 95% CI 1.22-11.23) in Aboriginal children, while Mcat increased the risk of OM in non-Aboriginal children (odds ratio = 2.63, 95% CI 1.32-5.23). Early carriage of Pnc was not associated with increased risk of OM.</p> <p>Conclusion</p> <p>Early NTHi carriage in Aboriginal children and Mcat in non-Aboriginal children is associated with increased risk of OM independent of environmental factors. In addition to addressing environmental risk factors for carriage such as overcrowding and exposure to environmental tobacco smoke, early administration of pneumococcal-<it>Haemophilus influenzae</it> D protein conjugate vaccine to reduce bacterial carriage in infants, may be beneficial for Aboriginal children; such an approach is currently being evaluated in Australia.</p> http://www.biomedcentral.com/1471-2334/12/366Otitis mediaAboriginal<it>Streptococcus pneumoniae</it><it>Haemophilus influenzae</it><it>Moraxella catarrhalis</it>
collection DOAJ
language English
format Article
sources DOAJ
author Sun Wenxing
Jacoby Peter
Riley Thomas V
Bowman Jacinta
Leach Amanda Jane
Coates Harvey
Weeks Sharon
Cripps Allan
Lehmann Deborah
spellingShingle Sun Wenxing
Jacoby Peter
Riley Thomas V
Bowman Jacinta
Leach Amanda Jane
Coates Harvey
Weeks Sharon
Cripps Allan
Lehmann Deborah
Association between early bacterial carriage and otitis media in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia: a cohort study
BMC Infectious Diseases
Otitis media
Aboriginal
<it>Streptococcus pneumoniae</it>
<it>Haemophilus influenzae</it>
<it>Moraxella catarrhalis</it>
author_facet Sun Wenxing
Jacoby Peter
Riley Thomas V
Bowman Jacinta
Leach Amanda Jane
Coates Harvey
Weeks Sharon
Cripps Allan
Lehmann Deborah
author_sort Sun Wenxing
title Association between early bacterial carriage and otitis media in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia: a cohort study
title_short Association between early bacterial carriage and otitis media in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia: a cohort study
title_full Association between early bacterial carriage and otitis media in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia: a cohort study
title_fullStr Association between early bacterial carriage and otitis media in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia: a cohort study
title_full_unstemmed Association between early bacterial carriage and otitis media in Aboriginal and non-Aboriginal children in a semi-arid area of Western Australia: a cohort study
title_sort association between early bacterial carriage and otitis media in aboriginal and non-aboriginal children in a semi-arid area of western australia: a cohort study
publisher BMC
series BMC Infectious Diseases
issn 1471-2334
publishDate 2012-12-01
description <p>Abstract</p> <p>Background</p> <p><it>Streptococcus pneumoniae</it> (Pnc), nontypeable <it>Haemophilus influenzae</it> (NTHi) and <it>Moraxella catarrhalis</it> (Mcat) are the most important bacterial pathogens associated with otitis media (OM). Previous studies have suggested that early upper respiratory tract (URT) bacterial carriage may increase risk of subsequent OM. We investigated associations between early onset of URT bacterial carriage and subsequent diagnosis of OM in Aboriginal and non-Aboriginal children living in the Kalgoorlie-Boulder region located in a semi-arid zone of Western Australia.</p> <p>Methods</p> <p>Aboriginal and non-Aboriginal children who had nasopharyngeal aspirates collected at age 1- < 3 months and at least one clinical examination for OM by an ear, nose and throat specialist before age 2 years were included in this analysis. Tympanometry to detect middle ear effusion was also performed at 2- to 6-monthly scheduled field visits from age 3 months. Multivariate regression models were used to investigate the relationship between early carriage and subsequent diagnosis of OM controlling for environmental factors.</p> <p>Results</p> <p>Carriage rates of Pnc, NTHi and Mcat at age 1- < 3 months were 45%, 29% and 48%, respectively, in 66 Aboriginal children and 14%, 5% and 18% in 146 non-Aboriginal children. OM was diagnosed at least once in 71% of Aboriginal children and 43% of non-Aboriginal children. After controlling for age, sex, presence of other bacteria and environmental factors, early nasopharyngeal carriage of NTHi increased the risk of subsequent OM (odds ratio = 3.70, 95% CI 1.22-11.23) in Aboriginal children, while Mcat increased the risk of OM in non-Aboriginal children (odds ratio = 2.63, 95% CI 1.32-5.23). Early carriage of Pnc was not associated with increased risk of OM.</p> <p>Conclusion</p> <p>Early NTHi carriage in Aboriginal children and Mcat in non-Aboriginal children is associated with increased risk of OM independent of environmental factors. In addition to addressing environmental risk factors for carriage such as overcrowding and exposure to environmental tobacco smoke, early administration of pneumococcal-<it>Haemophilus influenzae</it> D protein conjugate vaccine to reduce bacterial carriage in infants, may be beneficial for Aboriginal children; such an approach is currently being evaluated in Australia.</p>
topic Otitis media
Aboriginal
<it>Streptococcus pneumoniae</it>
<it>Haemophilus influenzae</it>
<it>Moraxella catarrhalis</it>
url http://www.biomedcentral.com/1471-2334/12/366
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