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Published on: November 2, 2020
A multicenter, randomized, controlled trial of dexamethasone for bronchiolitis
Howard M Corneli1, Joseph J Zorc, Prashant Mahajan
1University of Utah, Salt Lake City, USA.
Insights
A single dose of dexamethasone did not significantly reduce hospital admissions for infants with moderate-to-severe bronchiolitis. This study found no significant difference in respiratory status or later outcomes between dexamethasone and placebo groups.
Area of Science:
- Pediatrics
- Infectious Diseases
- Pharmacology
Background:
- Bronchiolitis is a common infant respiratory infection and a leading cause of childhood hospitalization.
- Corticosteroid use for bronchiolitis is common, but evidence supporting its efficacy is limited.
Purpose of the Study:
- To evaluate the effectiveness of a single oral dose of dexamethasone in treating moderate-to-severe bronchiolitis in infants.
- To determine if dexamethasone impacts hospital admission rates, respiratory status, or subsequent medical outcomes.
Main Methods:
- A double-blind, randomized trial involving 600 infants (2-12 months) with moderate-to-severe bronchiolitis.
- Comparison of a single 1 mg/kg oral dose of dexamethasone versus placebo.
- Primary outcome: hospital admission after 4-hour emergency department observation; secondary outcomes included respiratory status and later medical events.
Main Results:
- Hospital admission rates were similar: 39.7% for dexamethasone vs. 41.0% for placebo (absolute difference -1.3%).
- No significant difference in respiratory improvement after 4 hours (mean RACS -5.3 vs. -4.8).
- Multivariate analysis and evaluation of later outcomes (hospital stay, subsequent visits/admissions) showed no significant differences between groups.
Conclusions:
- A single oral dose of dexamethasone does not significantly alter hospital admission rates in infants with acute moderate-to-severe bronchiolitis.
- Dexamethasone did not improve respiratory status after 4 hours of observation or affect later medical outcomes.
- The findings suggest limited benefit of this corticosteroid regimen for hospitalized infants with bronchiolitis.
Background:
Bronchiolitis, the most common infection of the lower respiratory tract in infants, is a leading cause of hospitalization in childhood. Corticosteroids are commonly used to treat bronchiolitis, but evidence of their effectiveness is limited.
Methods:
We conducted a double-blind, randomized trial comparing a single dose of oral dexamethasone (1 mg per kilogram of body weight) with placebo in 600 children (age range, 2 to 12 months) with a first episode of wheezing diagnosed in the emergency department as moderate-to-severe bronchiolitis (defined by a Respiratory Distress Assessment Instrument score > or =6). We enrolled patients at 20 emergency departments during the months of November through April over a 3-year period. The primary outcome was hospital admission after 4 hours of emergency department observation. The secondary outcome was the Respiratory Assessment Change Score (RACS). We also evaluated later outcomes: length of hospital stay, later medical visits or admissions, and adverse events.
Results:
Baseline characteristics were similar in the two groups. The admission rate was 39.7% for children assigned to dexamethasone, as compared with 41.0% for those assigned to placebo (absolute difference, -1.3%; 95% confidence interval [CI], -9.2 to 6.5). Both groups had respiratory improvement during observation; the mean 4-hour RACS was -5.3 for dexamethasone, as compared with -4.8 for placebo (absolute difference, -0.5; 95% CI, -1.3 to 0.3). Multivariate adjustment did not significantly alter the results, nor were differences detected in later outcomes.
Conclusions:
In infants with acute moderate-to-severe bronchiolitis who were treated in the emergency department, a single dose of 1 mg of oral dexamethasone per kilogram did not significantly alter the rate of hospital admission, the respiratory status after 4 hours of observation, or later outcomes. (ClinicalTrials.gov number, NCT00119002 [ClinicalTrials.gov].).
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