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    Impact of lung disease on respiratory impedance in young children with cystic fibrosis

    Access Status
    Open access via publisher
    Authors
    Ramsey, K.
    Ranganathan, S.
    Gangell, C.
    Turkovic, L.
    Park, J.
    Skoric, B.
    Stick, S.
    Sly, P.
    Hall, Graham
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Ramsey, K. and Ranganathan, S. and Gangell, C. and Turkovic, L. and Park, J. and Skoric, B. and Stick, S. et al. 2015. Impact of lung disease on respiratory impedance in young children with cystic fibrosis. European Respiratory Journal. 46 (6): pp. 1672-1679.
    Source Title
    European Respiratory Journal
    DOI
    10.1183/13993003.00156-2015
    ISSN
    0903-1936
    School
    School of Physiotherapy and Exercise Science
    URI
    http://hdl.handle.net/20.500.11937/54512
    Collection
    • Curtin Research Publications
    Abstract

    This study aimed to evaluate the ability of the forced oscillation technique (FOT) to detect underlying lung disease in preschool children with cystic fibrosis (CF) diagnosed following newborn screening. 184 children (aged 3–6 years) with CF underwent lung function testing on 422 occasions using the FOT to assess respiratory resistance and reactance at the time of their annual bronchoalveolar lavage collection and chest computed tomography scan. We examined associations between FOT outcomes and the presence and progression of respiratory inflammation, infection and structural lung disease. Children with CF who had pronounced respiratory disease, including free neutrophil elastase activity, infection with pro-inflammatory pathogens and structural lung abnormalities had similar FOT outcomes to those children without detectable lung disease. In addition, the progression of lung disease over 1 year was not associated with worsening FOT outcomes. We conclude that the forced oscillation technique is relatively insensitive to detect underlying lung disease in preschool children with CF. However, FOT may still be of value in improving our understanding of the physiological changes associated with early CF lung disease.

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