Several studies have demonstrated that normal infants exhibit bronchoconstr
iction after inhalation of nonspecific agonists and that the induced airway
narrowing can be reversed by the inhalation of a beta -agonist. However, t
here are very limited data on baseline airway tone and the airway response
to a beta -agonist in this subject population. The purpose of our study was
to evaluate in normal infants baseline airway responsiveness to the inhale
d beta -agonist, albuterol, using changes in maximal expiratory flows. Fort
y-one healthy infant volunteers with no history of respiratory disease or r
ecurrent wheezing (ages 5.4 to 141.4 wk) were studied. Maximal expiratory f
low-volume curves were obtained at baseline and 10 min after inhalation of
albuterol (n = 28) or placebo (n = 13) using a metered-dose inhaler with a
spacer. The mean percent change was significantly greater (p < 0.05) in the
albuterol versus placebo group for FEV0.5 (2.2% versus -1.5%), FEF75% (10.
6% versus -3.1%), and FEF85% (12.9% versus 0.5%). Six of 28 albuterol-treat
ed infants demonstrated increases in FEF75% greater than two standard devia
tions from the mean change in FEF75% seen in the placebo group. These infan
ts were younger and more frequently exposed to maternal smoking during preg
nancy. We conclude that normal healthy infants have overall levels of basel
ine airway tone that are similar to that reported in adults and older child
ren; however, among the infants we evaluated the response to an inhaled bro
nchodilator was greatest in the youngest infants and in those exposed to to
bacco smoking.