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ObjectiveThe clinical benefit of newborn screening (NBS) for cystic fibrosis (CF) has been primarily nutritional, with less overt respiratory impact. Identification of risk factors for infant CF lung disease could facilitate targeted interventions to improve pulmonary outcomes.
MethodsThis retrospective study evaluated socioeconomic information, clinical data, and results from routine infant pulmonary...
ObjectivesThe evidence linking socioeconomic status (SES) and adherence in cystic fibrosis (CF) is inconclusive and focused on medication uptake. We examined associations between SES, adherence to airway clearance therapy (ACT), and CF respiratory outcomes.
Study DesignSocioeconomic, clinical, and adherence data of CF patients (N = 110) at a single CF Center were evaluated in this cross‐sectional...
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