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Title: | Recovery of lung function following a pulmonary exacerbation in patients with cystic fibrosis and the G551D-CFTR mutation treated with ivacaftor | Authors: | Wagener, J. S. Flume, P. A. Wainwright, Claire Elizabeth Tullis, D. Rodriguez, S. Niknian, M. Higgins, M. Davies, J. C. |
Issue Date: | 2018 | Source: | 17, (1), 2018, p. 83-88 | Pages: | 83-88 | Journal: | Journal of Cystic Fibrosis | Abstract: | Background 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 | DOI: | 10.1016/j.jcf.2017.06.002 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L616979602&from=exporthttp://dx.doi.org/10.1016/j.jcf.2017.06.002 | | Keywords: | article;child;clinical feature;cystic fibrosis;disease exacerbation;forced expiratory volume;functional assessment;gene mutation;human;cystic fibrosis transmembrane conductance regulator;lung disease;lung function;major clinical study;symptomatology;treatment outcome;NCT00909532antibiotic agent;incidence;ivacaftor;placebo;adolescent | Type: | Article |
Appears in Sites: | Children's Health Queensland Publications |
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