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    Multiple-breath washout as a lung function test in cystic fibrosis: A cystic fibrosis foundation workshop report

    Access Status
    Fulltext not available
    Authors
    Subbarao, P.
    Milla, C.
    Aurora, P.
    Davies, J.
    Davis, S.
    Hall, Graham
    Heltshe, S.
    Latzin, P.
    Lindblad, A.
    Pittman, J.
    Robinson, P.
    Rosenfeld, M.
    Singer, F.
    Starner, T.
    Ratjen, F.
    Morgan, W.
    Date
    2015
    Type
    Journal Article
    
    Metadata
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    Citation
    Subbarao, P. and Milla, C. and Aurora, P. and Davies, J. and Davis, S. and Hall, G. and Heltshe, S. et al. 2015. Multiple-breath washout as a lung function test in cystic fibrosis: A cystic fibrosis foundation workshop report. Annals of the American Thoracic Society. 12 (6): pp. 932-939.
    Source Title
    Annals of the American Thoracic Society
    DOI
    10.1513/AnnalsATS.201501-021FR
    ISSN
    2325-6621
    School
    School of Physiotherapy and Exercise Science
    URI
    http://hdl.handle.net/20.500.11937/54367
    Collection
    • Curtin Research Publications
    Abstract

    The lung clearance index (LCI) is a lung function parameter derived from the multiple-breath washout (MBW) test. Although first developed 60 years ago, the technique was not widely used for many years. Recent technological advances in equipment design have produced gains in popularity for this test among cystic fibrosis (CF) researchers and clinicians, particularly for testing preschool-aged children. LCI has been shown to be feasible and sensitive to early CF lung disease in patients of all ages from infancy to adulthood. A workshop was convened in January 2014 by the North American Cystic Fibrosis Foundation to determine the readiness of the LCI for use in multicenter clinical trials as well as clinical care. The workshop concluded that the MBW text is a valuable potential outcome measure for CF clinical trials in preschool-aged patients and in older patients with FEV1 in the normal range. However, gaps in knowledge about the choice of device, gas, and standardization across systems are key issues precluding its use as a clinical trial end point in infants. Based on the current evidence, there are insufficient data to support the use of LCI or MBW parameters in the routine clinical management of patients with CF.

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