LONGITUDINAL EVALUATION OF PULMONARY-FUNCTION IN INFANTS AND VERY YOUNG-CHILDREN WITH CYSTIC-FIBROSIS

Thirty-two infants with cystic fibrosis (CF) had pulmonary function te sting and chest radiographs at the time of diagnosis and on average 1 year later, when they had no acute respiratory symptoms. At diagnosis, 14 of 32 infants had respiratory symptoms (RESP) and 18 did not have respiratory symptoms (NRESP). There were no significant differences in age, weight, or length between the RESP and NRESP groups. At diagnosi s, the RESP group had significantly lower forced expiratory flows comp ared to the NRESP group (41 +/- 32% vs. 98 +/- 48% predicted); however , there were no significant differences in functional residual capacit y or chest radiographic scores. Between diagnosis and follow-up, the N RESP group had no significant change in pulmonary function but a decli ne in chest roentgenographic (CXR) scores (22 +/- 2 to 21 +/- 2). For infants in the RESP group, there were no significant changes in FRC or CXR score. Maximal expiratory flow at functional residual capacity (V max FRC) rose from diagnosis to 1 year follow-up (41 +/- 32 % to 74 +/ - 27 % predicted; P < 0.002); however, at follow-up flows for the RESP group remained significantly lower than flows for the NRESP group (74 % vs. 113 % predicted; P < 0.0005). For the 32 infants with CF, there was significant correlation between percent predicted Vmax FRC at fol low-up and at diagnosis (r = 0.47; P < 0.02). Those infants with lower percent predicted flows at diagnosis were more likely to have lower p ercent predicted flows 1 year later. Flows at follow-up were not relat ed to a family history of asthma or to passive smoke exposure. We conc lude that the potential benefits of early diagnosis by neonatal screen ing and the choice of therapeutic interventions early in life will dep end upon the causes of the relationship between low flows at diagnosis and at follow-up. (C) 1993 Wiley-Wiss, Inc.