Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4378
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dc.contributor.authorWagener, J. S.en
dc.contributor.authorFlume, P. A.en
dc.contributor.authorWainwright, Claireen
dc.contributor.authorElizabeth Tullis, D.en
dc.contributor.authorRodriguez, S.en
dc.contributor.authorNiknian, M.en
dc.contributor.authorHiggins, M.en
dc.contributor.authorDavies, J. C.en
dc.date.accessioned2022-11-07T23:52:12Z-
dc.date.available2022-11-07T23:52:12Z-
dc.date.issued2018en
dc.identifier.citation17, (1), 2018, p. 83-88en
dc.identifier.otherRISen
dc.identifier.urihttp://dora.health.qld.gov.au/qldresearchjspui/handle/1/4378-
dc.description.abstractBackground Pulmonary exacerbations (PEx) are associated with acute loss of lung function that is often not recovered after treatment. We investigated lung function recovery following PEx for ivacaftor- and placebo-treated subjects. Methods Short- and long-term pulmonary function recovery data after PEx were summarized from a placebo-controlled trial in 161 cystic fibrosis patients ≥ 12 years old with the G551D-CFTR mutation (NCT00909532). Short-term recovery was measured 2 to 8 weeks after treatment, and long-term recovery was determined at the end-of-study, both compared with baseline measured just prior to the PEx. Results Fewer patients receiving ivacaftor experienced a PEx than patients receiving placebo (33.7% vs. 56.4%; P = 0.004) and had a lower adjusted incidence rate of PEx (0.589 vs. 1.382; P < 0.001). The proportion of PEx followed by full short-term recovery of percent predicted forced expiratory volume in 1 s was similar (ivacaftor vs. placebo, 57.1% vs. 53.7), as was the proportion of patients having long-term recovery (46.4% vs. 47.7%). Conclusions Ivacaftor treatment reduces the frequency of PEx but does not improve on the rate of complete lung function recovery after PEx when compared with placebo.L6169796022017-06-30 <br />2018-01-12 <br />en
dc.language.isoenen
dc.relation.ispartofJournal of Cystic Fibrosisen
dc.titleRecovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftoren
dc.typeArticleen
dc.identifier.doi10.1016/j.jcf.2017.06.002en
dc.subject.keywordsarticleen
dc.subject.keywordschilden
dc.subject.keywordsclinical featureen
dc.subject.keywordscystic fibrosisen
dc.subject.keywordsdisease exacerbationen
dc.subject.keywordsforced expiratory volumeen
dc.subject.keywordsfunctional assessmenten
dc.subject.keywordsgene mutationen
dc.subject.keywordshumanen
dc.subject.keywordscystic fibrosis transmembrane conductance regulatoren
dc.subject.keywordslung diseaseen
dc.subject.keywordslung functionen
dc.subject.keywordsmajor clinical studyen
dc.subject.keywordssymptomatologyen
dc.subject.keywordstreatment outcomeen
dc.subject.keywordsNCT00909532antibiotic agenten
dc.subject.keywordsincidenceen
dc.subject.keywordsivacaftoren
dc.subject.keywordsplaceboen
dc.subject.keywordsadolescenten
dc.relation.urlhttps://www.embase.com/search/results?subaction=viewrecord&id=L616979602&from=exporthttp://dx.doi.org/10.1016/j.jcf.2017.06.002 |en
dc.identifier.risid1782en
dc.description.pages83-88en
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
Appears in Sites:Children's Health Queensland Publications
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