Preliminary data show improved lung function in children and young adults with cystic fibrosis after ETI treatment, suggesting new assessment methods.
Our preliminary data suggest that oscillometry parameters showed a significant improvement after ETI treatment among all genotype groups. More data are required to assess whether and which FOT parameters could be used as surrogates of LCI or spirometry for the long-term follow-up of pwCF.
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Kogias et al. (2026) studied this question.
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