The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis

This study aimed to investigate the evolution of airway function in infants newly diagnosed with cystic fibrosis (CF). FEV0.5 was measured soon after diagnosis (median age of 28 weeks) and 6 months later in subjects with CIF and on two occasions 6 months apart (median ages of 7.4 and 33.7 weeks) in healthy infants, using the raised-volume technique. Repeated measurements were successful in 34 CF and 32 healthy subjects. After adjustment for age, length, sex, and exposure to maternal smoking, mean FEV0.5 was significantly lower in infants with CF both shortly after diagnosis and at the second test, with no significant difference in rate of increase in FEV0.5 with growth between the two groups. When compared with published reference data, FEV0.5 was reduced by an average of two z scores on both test occasions in those with CF, with 72% of individuals having an FEV0.5 of less than 1.64 z-scores (i.e., less than the fifth percentile) on one or both test occasions. On longitudinal analysis, subjects with CF experienced a mean (95% confidence interval) reduction in FEV0.5 of 20% (11, 28). Airway function is diminished soon after diagnosis in infants with CF and does not catch up during infancy and early childhood. These findings have important implications for early interventions in CF.