A follow-up study was conducted in 40 children who had been enrolled in a p
rospective randomized study of exogenous surfactant therapy for respiratory
distress syndrome (RDS) (n = 22; S) or placebo (n = 18; P) to determine lo
ng-term pulmonary sequelae of surfactant treatment in premature infants wit
h RDS. At follow-up, mean (SD) age was 6.63 (0.18) and 6.55 (0.23) years fo
r S and P, respectively. Complete lung function tests (LFT) were attempted
in all patients.
Satisfactory data were obtained in 17/22 surfactant-treated and in 12/18 co
ntrol children. There was no significant difference between groups for any
of the parameters measured. Mean (SD) functional residual capacity (FRC) wa
s 92% (16%) and 90% (21%) predicted, mean (SD) airway resistance (R-aw,R-ex
p) was 122% (25%) and 127% (61%), and mean (SD) forced expiratory volume in
1 s (FEV1) was 104% (12%) and 99% (17%) predicted for S and P. Only maxima
l expiratory flow at 25% vital capacity (L/s) was significantly below the p
redicted range in S and P groups, with 74% (23%) and 77% (28%), respectivel
y. To test bronchial hyperreactivity, a simple standardized running test wa
s performed: 4 children in S and 5 in P showed a significant response as de
fined by clinical airway obstruction or changes in FEV1 and/or R-aw, with n
o significant difference between groups.
Although we found no major abnormalities in lung function and no difference
between S and P at early school-age, lack of cooperation during lung Funct
ion tests makes further follow-up necessary. (C) 1999 Wiley-Liss, Inc.