Objective: To assess the efficacy of oral dexamethasone or nebulized dexame
thasone sodium phosphate in children with mild croup.
Methods: Double-blind, placebo-controlled study of 264 children between 6 m
onths and 6 years of age with symptoms of croup for fewer than 48 hours. Pa
tients were excluded if they received racemic epinephrine or corticosteroid
treatment. Other exclusion criteria included corticosteroid treatment duri
ng the 14 days prior to enrollment or complicating medical condition. Subje
cts randomly received oral dexamethasone (0.6 mg/kg), nebulized dexamethaso
ne sodium phosphate (160 mug), or placebo. Telephone follow-up was obtained
on days 1, 2, 3, 4, and 7.
Main Outcome Measures: The primary outcome measure was treatment failure, d
efined as receiving corticosteroid or racemic epinephrine treatment during
the 7 days after enrollment in the study. Secondary outcome measures includ
ed seeking additional care and the parental assessments of the patients' co
ndition obtained during follow-up (worse, same, better, or gone).
Results: Eighty-five patients received oral dexamethasone, 91 received nebu
lized dexamethasone, and 88 received placebo. There were 3 treatment failur
es in the oral dexamethasone-treated group, 12 in the nebulized dexamethaso
ne-treated group, and 10 in the placebo-treated group (P = .05). Ten childr
en in the oral dexamethasone-treated group sought additional care compared
with 27 and 29 in the nebulized dexamethasone-treated and placebo-treated g
roups, respectively (P = .002). Parents of children in the oral dexamethaso
ne-treated group reported greater improvement on day 1 (P < .001) compared
with the nebulized dexamethasone-treated and placebo-treated groups.
Conclusions: Children with mild croup who receive oral dexamethasone treatm
ent are less likely to seek subsequent medical care and demonstrate more ra
pid symptom resolution compared with children who receive nebulized dexamet
hasone or placebo treatment.