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Updated: May 22, 2026

Murine Model of Allergen Induced Asthma
Published on: May 14, 2012
Oral prednisolone for preschool children with acute virus-induced wheezing
Jayachandran Panickar1, Monica Lakhanpaul, Paul C Lambert
1Division of Child Health, University of Leicester, Leicester, United Kingdom.
Insights
Oral prednisolone did not significantly improve hospitalization duration for preschool children with viral-induced wheezing. This common treatment showed no benefit over placebo in a randomized controlled trial.
Area of Science:
- Pediatrics
- Respiratory Medicine
- Clinical Trials
Background:
- Wheezing attacks are common in preschool children due to viral infections.
- Oral prednisolone is frequently prescribed for these cases, but its effectiveness is debated.
Purpose of the Study:
- To evaluate the efficacy of a 5-day course of oral prednisolone compared to placebo in preschool children hospitalized with viral-induced wheezing.
Main Methods:
- A randomized, double-blind, placebo-controlled trial involving 700 children (10 months to 60 months old).
- Participants received either oral prednisolone or placebo for 5 days.
- Primary outcome: duration of hospitalization; Secondary outcomes: Preschool Respiratory Assessment Measure score, albuterol use, and symptom scores.
Main Results:
- No significant difference in hospitalization duration between the prednisolone and placebo groups (11.0 hours vs. 13.9 hours).
- No significant differences observed in secondary outcomes or adverse events between the groups.
Conclusions:
- Oral prednisolone is not superior to placebo for treating mild-to-moderate wheezing associated with viral infections in preschool children presenting to hospitals.
Background:
Attacks of wheezing induced by upper respiratory viral infections are common in preschool children between the ages of 10 months and 6 years. A short course of oral prednisolone is widely used to treat preschool children with wheezing who present to a hospital, but there is conflicting evidence regarding its efficacy in this age group.
Methods:
We conducted a randomized, double-blind, placebo-controlled trial comparing a 5-day course of oral prednisolone (10 mg once a day for children 10 to 24 months of age and 20 mg once a day for older children) with placebo in 700 children between the ages of 10 months and 60 months. The children presented to three hospitals in England with an attack of wheezing associated with a viral infection; 687 children were included in the intention-to-treat analysis (343 in the prednisolone group and 344 in the placebo group). The primary outcome was the duration of hospitalization. Secondary outcomes were the score on the Preschool Respiratory Assessment Measure, albuterol use, and a 7-day symptom score.
Results:
There was no significant difference in the duration of hospitalization between the placebo group and the prednisolone group (13.9 hours vs. 11.0 hours; ratio of geometric means, 0.90; 95% confidence interval, 0.77 to 1.05) or in the interval between hospital admission and signoff for discharge by a physician. In addition, there was no significant difference between the two study groups for any of the secondary outcomes or for the number of adverse events.
Conclusions:
In preschool children presenting to a hospital with mild-to-moderate wheezing associated with a viral infection, oral prednisolone was not superior to placebo. (Current Controlled Trials number, ISRCTN58363576.)
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