Persistent Bacterial Bronchitis: time to venture beyond the Umbrella
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Published version
Author(s)
Bush, Andrew
Type
Journal Article
Abstract
Chronic cough in children is common and frequently mismanaged. In the past, cough
was diagnosed as asthma and inappropriate asthma therapies prescribed and esca-
lated. It has been realized that persistent bacterial bronchitis (PBB) is a common cause
of wet cough and responds to oral antibiotics. The initial definition comprised a history
of chronic wet cough, positive bronchoalveolar (BAL) cultures for a respiratory pathogen
and response to a 2-week course of oral amoxicillin–clavulanic acid. This is now termed
PBB-micro; PBB-clinical eliminates the need for BAL. PBB-extended is PBB-micro or
PBB-clinical but resolution necessitating 4 weeks of antibiotics; and recurrent PBB is
>
3 attacks of PBB-micro or-clinical/year. However, the airway has only a limited range
of responses to chronic inflammation and infection, and neutrophilic airway disease is
seen in many other conditions, such as cystic fibrosis and primary ciliary dyskinesia,
both chronic suppurative lung disease endotypes, whose recognition has led to huge
scientific and clinical advances. There is an urgent need to extend endotyping into PBB,
especially PBB-recurrent. We need to move from associative studies and, in particular,
deploy sophisticated modern –omics technologies and systems biology, rather as has
been done in the context of asthma in U-BIOPRED. In summary, the use of the term
PBB has done signal service in pointing us away from prescribing asthma therapies to
children with infected airways, but we now need to move beyond a simple description to
teasing out underlying endotypes.
was diagnosed as asthma and inappropriate asthma therapies prescribed and esca-
lated. It has been realized that persistent bacterial bronchitis (PBB) is a common cause
of wet cough and responds to oral antibiotics. The initial definition comprised a history
of chronic wet cough, positive bronchoalveolar (BAL) cultures for a respiratory pathogen
and response to a 2-week course of oral amoxicillin–clavulanic acid. This is now termed
PBB-micro; PBB-clinical eliminates the need for BAL. PBB-extended is PBB-micro or
PBB-clinical but resolution necessitating 4 weeks of antibiotics; and recurrent PBB is
>
3 attacks of PBB-micro or-clinical/year. However, the airway has only a limited range
of responses to chronic inflammation and infection, and neutrophilic airway disease is
seen in many other conditions, such as cystic fibrosis and primary ciliary dyskinesia,
both chronic suppurative lung disease endotypes, whose recognition has led to huge
scientific and clinical advances. There is an urgent need to extend endotyping into PBB,
especially PBB-recurrent. We need to move from associative studies and, in particular,
deploy sophisticated modern –omics technologies and systems biology, rather as has
been done in the context of asthma in U-BIOPRED. In summary, the use of the term
PBB has done signal service in pointing us away from prescribing asthma therapies to
children with infected airways, but we now need to move beyond a simple description to
teasing out underlying endotypes.
Date Issued
2017-12-11
Date Acceptance
2017-11-27
Citation
FRONTIERS IN PEDIATRICS, 2017, 5
ISSN
2296-2360
Publisher
FRONTIERS MEDIA SA
Journal / Book Title
FRONTIERS IN PEDIATRICS
Volume
5
Copyright Statement
© 2017 Bush. This is an open-access article distributed under the terms
of the Creative Commons Attribution License (CC BY https://creativecommons.org/licenses/by/4.0/). The use, distribution or
reproduction in other forums is permitted, provided the original author(s) or licensor
are credited and that the original publication in this journal is cited, in accordance
with accepted academic practice. No use, distribution or reproduction is permitted
which does not comply with these terms.
of the Creative Commons Attribution License (CC BY https://creativecommons.org/licenses/by/4.0/). The use, distribution or
reproduction in other forums is permitted, provided the original author(s) or licensor
are credited and that the original publication in this journal is cited, in accordance
with accepted academic practice. No use, distribution or reproduction is permitted
which does not comply with these terms.
Sponsor
Asthma UK
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000417601400001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Grant Number
R43065
Subjects
Science & Technology
Life Sciences & Biomedicine
Pediatrics
cystic fibrosis
primary ciliary dyskinesia
endotype
airway infection
airway inflammation
bronchoalveolar lavage
PRIMARY CILIARY DYSKINESIA
CYSTIC-FIBROSIS GENE
CHRONIC WET COUGH
INHALED CORTICOSTEROIDS
YOUNG-CHILDREN
INDUCED SPUTUM
RISK-FACTORS
ASTHMA
BRONCHIECTASIS
DISEASE
Publication Status
Published
Article Number
ARTN 264