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The effect of montelukast on respiratory symptoms and lung function in wheezy infants
Anna S Pelkonen1, Kristiina Malmström, Seppo Sarna
1Helsinki University Central Hospital, Helsinki, Finland. anna.pelkonen@hus.fi
Insights
Montelukast did not improve symptom-free days for infants with recurrent wheezing. This asthma medication showed no significant benefits in lung function or airway inflammation in young children.
Area of Science:
- Pediatric Pulmonology
- Pharmacology
Background:
- Recurrent wheezing is common in infants, impacting quality of life.
- Montelukast is a leukotriene receptor antagonist used for asthma management.
Purpose of the Study:
- To evaluate the efficacy of montelukast in infants aged 6-24 months with recurrent wheezing.
- To assess montelukast's impact on symptom-free days, rescue medication use, lung function, and airway inflammation.
Main Methods:
- A randomized, placebo-controlled trial involving 113 infants.
- Daily administration of montelukast or placebo for 8 weeks.
- Primary endpoint: symptom-free days. Secondary endpoints: rescue medication use, lung function (FRC, sGaw, V'max,FRC), airway responsiveness, and exhaled nitric oxide fraction (FeNO).
Main Results:
- No significant difference in symptom-free days between montelukast and placebo groups (p = 0.965).
- No significant differences observed in rescue medication use, lung function parameters, airway responsiveness, or FeNO levels.
- Montelukast did not demonstrate clinical efficacy in this pediatric population.
Conclusions:
- Montelukast therapy is not effective for managing recurrent wheezing in infants.
- The study suggests no benefit of montelukast on symptom control, lung function, or airway inflammation in this age group.
Abstract:
Our aim was to investigate the effectiveness of montelukast in recurrently wheezy infants. We randomised 113, 6-24-month-old children with recurrent wheezing to receive either placebo or montelukast daily for an 8-week period. The primary end-point was symptom-free days. The secondary aims were to evaluate the effect of montelukast on rescue medication, on lung function, airway responsiveness and exhaled nitric oxide fraction (FeNO). Clinical response and FeNO were determined, the functional residual capacity (FRC) and specific airway conductance (sGaw) were measured using an infant whole-body plethysmograph, the maximal flow at functional residual capacity (V'max,FRC) was recorded using the squeeze technique and airway responsiveness was evaluated by performing a dosimetric methacholine challenge test. There was no significant difference in changes in weekly symptom-free days between the montelukast and the placebo group (3.1-3.7 days versus 2.7-3.1 days, p = 0.965). No significant differences were detected in the secondary end-points, i.e. use of rescue medication, FRC, sGaw, V'max,FRC, FeNO or airway responsiveness between groups. Montelukast therapy did not influence the number of symptom-free days, use of rescue medication, lung function, airway responsiveness or airway inflammation in recurrently wheezy, very young children.
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