Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis: A Cystic Fibrosis Foundation Workshop Report

dc.contributor.authorSubbarao, Padmaja
dc.contributor.authorMilla, Carlos
dc.contributor.authorAurora, Paul
dc.contributor.authorDavies, Jane C.
dc.contributor.authorDavis, Stephanie D.
dc.contributor.authorHall, Graham L.
dc.contributor.authorHeltshe, Sonya
dc.contributor.authorLatzin, Philipp
dc.contributor.authorLindblad, Anders
dc.contributor.authorPittman, Jessica E.
dc.contributor.authorRobinson, Paul D.
dc.contributor.authorRosenfeld, Margaret
dc.contributor.authorSinger, Florian
dc.contributor.authorStarner, Tim D.
dc.contributor.authorRatjen, Felix
dc.contributor.authorMorgan, Wayne
dc.contributor.departmentDepartment of Pediatrics, IU School of Medicineen_US
dc.date.accessioned2016-04-22T14:26:57Z
dc.date.available2016-04-22T14:26:57Z
dc.date.issued2015-06
dc.description.abstractThe 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.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationSubbarao, P., Milla, C., Aurora, P., Davies, J. C., Davis, S. D., Hall, G. L., … Morgan, W. (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), 932–939. http://doi.org/10.1513/AnnalsATS.201501-021FRen_US
dc.identifier.urihttps://hdl.handle.net/1805/9378
dc.language.isoenen_US
dc.relation.isversionof10.1513/AnnalsATS.201501-021FRen_US
dc.relation.journalAnnals of the American Thoracic Societyen_US
dc.rightsPublisher Policyen_US
dc.sourceAuthoren_US
dc.subjectmultiple-breath washouten_US
dc.subjectlung clearance indexen_US
dc.subjectcystic fibrosisen_US
dc.titleMultiple-Breath Washout as a Lung Function Test in Cystic Fibrosis: A Cystic Fibrosis Foundation Workshop Reporten_US
dc.typeArticleen_US
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