Background Shared decision‐making is important in child and adolescent healthcare
because there is growing international recognition of children and young people's rights to …

Introduction. Optimizing nutrition remains the cornerstone of therapy for patients with cystic
fibrosis (CF) since it is associated with better pulmonary function and survival. However, a …

Introduction There is a strong association between cystic fibrosis and malnutrition, mainly
because of the higher energy needs combined with lower intake. There is also a well …

Background Intestinal dysbiosis has been described in Cystic Fibrosis (CF) and probiotics
have been proposed to restore microbial composition. Aim of the study was to investigate …

Background Evidence on the effectiveness of proton pump inhibitors (PPI) as adjuvant
therapy to improve maldigestion in people with cystic fibrosis (pwCF) is limited and there is …

Background Long-term effect of enteral tube feeding (ETF) in cystic fibrosis (CF) remains
equivocal. Methods A Belgian CF registry based, retrospective, longitudinal study, evaluated …

The aim of our study was to assess the nutritional status of hospitalized children with cystic
fibrosis. We extracted data from the ePINUT surveys. Undernutrition was defined as a body …

Background Cystic fibrosis (CF) is a disease in which nutritional barriers are diverse and
common, with malnutrition greatly influencing pulmonary trajectory and overall outcomes …

Background Nutrition is recognized as a modifiable contributor to bronchiectasis and
interstitial lung diseases (ChILD) development and progression. Nutritional interventions …

Abnormal functioning of the Cystic Fibrosis (CF) Transmembrane Conductance Regulator
(CFTR) channel impairs mucociliary clearance and promotes chronic bacterial infections in …