References 1 Nixon GM, Armstrong DS, Carzino R, et al. Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis. J Pediatr 2001; 138: 699–704. 2 Emerson J, Rosenfeld M, McNamara S, et al. Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. Pediatr Pulmonol 2002; 34: 91–100. 3 Frederiksen B, Koch C, Hoiby N. Antib...

The fluorescein dilaurate test, a non-invasive test of exocrine pancreatic function, was carried out on 21 children with cystic fibrosis and pancreatic exocrine insufficiency, and 12 healthy siblings. The test clearly discriminated between the patients with cystic fibrosis and severe exocrine pancreatic insufficiency and the normal control subjects.

Background Cystic Fibrosis (CF) occurs randomly in children across all European social strata providing an opportunity to sample their underpinning health care provision for this rare disease in an unbiased manner. We developed a 35 country European cystic fibrosis (CF) demographic registry to compare CF outcomes through an FP6 programme of the EU called EuroCareCF (http://www. eurocarecf.eu).

Seven cases of cystic fibrosis complicated by chronic salt depletion and failure to thrive were studied. After replacement of the salt deficit, the metabolic abnormalities resolved, and weight gain was rapid. This should be considered as a differential diagnosis in children who have been diagnosed as having cystic fibrosis, but who fail to thrive despite standard treatment.

Activities of superoxide dismutase, catalase and glutathione peroxidase in erythrocytes of cystic fibrosis children were studied in order to estimate the severity of their deficiency. Our results point to increased susceptibility of erythrocytes of cystic fibrosis subjects to oxidative injury and indicate that the antioxidant status of patients should be carefully monitored.

cystic fibrosis (cf) is an autosomal recessive disease, which affects many organs as it impairs chloride channel. this study was performed to evaluate growth status and its relationship with some laboratory indices such as cholesterol (chol), triglyceride (tg), albumin and total protein in children with cf referred to pediatrics center. this study was designed as a cross-sectional study in one ...

background: cystic fibrosis (cf) is a common genetic disorder chiefly characterized by respiratory and gastrointestinal symptoms. the purpose of this study was to evaluate the clinical presentation and growth status in cf patients at the time of diagnosis and following conventional treatment. materials and methods: a cross-sectional study was conducted on 67 cf patients who enrolled for at leas...

OBJECTIVES Previous studies have examined renal safety of once daily intravenous tobramycin in individuals with cystic fibrosis. This has been mainly in combination with ceftazidime in an adolescent or adult population. In this report, we describe our institutional experience of once daily intravenous tobramycin in combination with a variety of second anti-pseudomonal antibiotics in children wi...

Studies on mucociliary clearance (MCC) in cystic fibrosis (CF) have produced conflicting results. This study aimed to differentiate primary (ion transport-related) from secondary (inflammatory) causes of delayed MCC in CF. Nasal MCC was measured in 50 children (CF, primary ciliary dyskinesia (PCD) and no respiratory disease). Nasal lavage fluid was analysed for interleukin (IL)-8 and tumour nec...

QUESTION : Can a session of exercise with incorporated expiratory manoeuvres substitute for a session of breathing techniques for airway clearance in children with cystic fibrosis? Are children with cystic fibrosis as co-operative and satisfied with the exercise regimen as with the breathing techniques?. DESIGN Randomised, cross-over trial with concealed allocation and intention-to-treat anal...