Abstract
Objectives: The impressive improvements of CFTR function by elexacaftor/tezacaftor/ivacaftor (ETI) result in remarkable changes of pulmonary function and structural lung disease. Whether these effects translate to changes of microbial patterns, an equally critical aspect of CF lung disease, remains to be shown. To examine the effect of ETI on Staphylococcus aureus (SA) and Pseudomonas aeruginosa (PA) detections in people with CF (pwCF) ≥12 years.
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