A decade on: Follow-up findings of indigenous children with bronchiectasis.

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dc.contributor.author McCallum, Gabrielle B
dc.contributor.author Singleton, Rosalyn J
dc.contributor.author Redding, Gregory J
dc.contributor.author Grimwood, Keith
dc.contributor.author Byrnes, Catherine A
dc.contributor.author Valery, Patricia C
dc.contributor.author Mobberley, Charmaine
dc.contributor.author Oguoma, Victor M
dc.contributor.author Eg, Kah Peng
dc.contributor.author Morris, Peter S
dc.contributor.author Chang, Anne B
dc.coverage.spatial United States
dc.date.accessioned 2022-06-27T00:28:41Z
dc.date.available 2022-06-27T00:28:41Z
dc.date.issued 2020-04
dc.identifier.citation (2020). Pediatric Pulmonology, 55(4), 975-985.
dc.identifier.issn 8755-6863
dc.identifier.uri https://hdl.handle.net/2292/60149
dc.description.abstract OBJECTIVE:The sole prospective longitudinal study of children with either chronic suppurative lung disease (CSLD) or bronchiectasis published in the current era was limited to a single center. We sought to extend this study by evaluating the longer-term clinical and lung function outcomes and their associated risk factors in Indigenous children of adolescents from Australia, Alaska, and New Zealand who participated in our previous CSLD or bronchiectasis studies during 2004-2010. METHODS:Between 2015 and 2018, we evaluated 131 out of 180 (72.8%) children of adolescents from the original studies at a single follow-up visit. We administered standardized questionnaires, reviewed medical records, undertook clinical examinations, performed spirometry, and scored available chest computed tomography scans. RESULTS:Participants were seen at a mean age of 12.3 years (standard deviation: 2.6) and a median of 9.0 years (range: 5.0-13.0) after their original recruitment. With increasing age, rates of acute lower respiratory infections (ALRI) declined, while lung function was mostly within population norms (median forced expiry volume in one-second = 90% predicted, interquartile range [IQR]: 81-105; forced vital capacity [FVC] = 98% predicted, IQR: 85-114). However, 43 out of 111 (38.7%) reported chronic cough episodes. Their overall global rating judged by symptoms, including ALRI frequency, examination findings, and spirometry was well (20.3%), stable (43.9%), or improved (35.8%). Multivariable regression identified household tobacco exposure and age at first ALRI-episode as independent risk factors associated with lower FVC% predicted values. CONCLUSION:Under our clinical care, the respiratory outcomes in late childhood or early adolescence are encouraging for these patient populations at high-risk of premature mortality. Prospective studies to further inform management throughout the life course into adulthood are now needed.
dc.format.medium Print-Electronic
dc.language eng
dc.publisher Wiley
dc.relation.ispartofseries Pediatric pulmonology
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher.
dc.rights.uri https://researchspace.auckland.ac.nz/docs/uoa-docs/rights.htm
dc.subject Humans
dc.subject Respiratory Tract Infections
dc.subject Suppuration
dc.subject Bronchiectasis
dc.subject Lung Diseases
dc.subject Cough
dc.subject Chronic Disease
dc.subject Vital Capacity
dc.subject Spirometry
dc.subject Risk Factors
dc.subject Longitudinal Studies
dc.subject Follow-Up Studies
dc.subject Prospective Studies
dc.subject Adolescent
dc.subject Adult
dc.subject Child
dc.subject Alaska
dc.subject Australia
dc.subject New Zealand
dc.subject Female
dc.subject Male
dc.subject Indigenous Peoples
dc.subject Indigenous
dc.subject children
dc.subject chronic suppurative lung disease
dc.subject Clinical Research
dc.subject Pediatric
dc.subject Vaccine Related
dc.subject Prevention
dc.subject Pediatric Research Initiative
dc.subject Lung
dc.subject Respiratory
dc.subject 3 Good Health and Well Being
dc.subject Science & Technology
dc.subject Life Sciences & Biomedicine
dc.subject Pediatrics
dc.subject Respiratory System
dc.subject CYSTIC-FIBROSIS BRONCHIECTASIS
dc.subject QUALITY-OF-LIFE
dc.subject LUNG-FUNCTION
dc.subject PEDIATRIC BRONCHIECTASIS
dc.subject VALIDATION
dc.subject CHILDHOOD
dc.subject 1117 Public Health and Health Services
dc.subject Clinical
dc.subject Public Health
dc.subject 1114 Paediatrics and Reproductive Medicine
dc.title A decade on: Follow-up findings of indigenous children with bronchiectasis.
dc.type Journal Article
dc.identifier.doi 10.1002/ppul.24696
pubs.issue 4
pubs.begin-page 975
pubs.volume 55
dc.date.updated 2022-05-26T02:48:07Z
dc.rights.holder Copyright: The author en
dc.identifier.pmid 32096916 (pubmed)
pubs.author-url https://www.ncbi.nlm.nih.gov/pubmed/32096916
pubs.end-page 985
pubs.publication-status Published
dc.rights.accessrights http://purl.org/eprint/accessRights/RestrictedAccess en
pubs.subtype Research Support, Non-U.S. Gov't
pubs.subtype Journal Article
pubs.subtype Research Support, N.I.H., Extramural
pubs.elements-id 795841
pubs.org-id Medical and Health Sciences
pubs.org-id School of Medicine
pubs.org-id Paediatrics Child & Youth Hlth
dc.identifier.eissn 1099-0496
pubs.record-created-at-source-date 2022-05-26
pubs.online-publication-date 2020-02-25


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