1. Montelukast improves asthma control in asthmatic children maintained on inhaled corticosteroids
- Author
-
Lynda C. Schneider, Beth Cronin, Sandra J. Downes, Charles Greene, T.J. Eller, Wanda Phipatanakul, and Anne-Marie Irani
- Subjects
Pulmonary and Respiratory Medicine ,Spirometry ,Cyclopropanes ,Male ,Allergy ,medicine.medical_specialty ,Leukotriene D4 ,Adolescent ,medicine.drug_class ,Immunology ,Pilot Projects ,Acetates ,Sulfides ,Placebo ,chemistry.chemical_compound ,Double-Blind Method ,immune system diseases ,Adrenal Cortex Hormones ,Internal medicine ,Forced Expiratory Volume ,Immunology and Allergy ,Medicine ,Humans ,Anti-Asthmatic Agents ,Child ,Montelukast ,Administration, Intranasal ,Asthma ,medicine.diagnostic_test ,business.industry ,Respiratory disease ,Drug Synergism ,medicine.disease ,respiratory tract diseases ,chemistry ,Anesthesia ,Quinolines ,Corticosteroid ,Leukotriene Antagonists ,Female ,business ,hormones, hormone substitutes, and hormone antagonists ,medicine.drug - Abstract
Background Because of potential toxicities of inhaled corticosteroid (ICS) use in pediatric asthma, alternative or steroid-sparing therapy is desirable. There are no previous studies evaluating montelukast's steroid-sparing effects in children with asthma. Objective To evaluate whether (1) montelukast as add-on therapy improves asthma symptom control and (2) montelukast provides steroid-sparing effects in children with asthma treated with low to moderate doses of ICS therapy. Methods In a double-blind, placebo-controlled trial, 36 children ages 6 to 14 years with symptomatic asthma maintained on a stable low to moderate dose of ICSs were randomly assigned to receive montelukast or matching placebo for 24 weeks after a run-in period of 2 weeks (period I). During the trial, subjects kept daily asthma diary cards and monthly spirometry was performed. After a 4 week add-on period (period II), the subjects completed a 20-week (period III) ICS tapering period based on a predetermined protocol. Results In period II, the difference in the number of rescue-free days was significantly higher in the montelukast group ( P = 0.0001), and the number of rescue-free days per week was also significantly higher in montelukast-treated subjects compared with placebo subjects ( P = 0.002). In period III, the percentage reduction in ICS dose was not significant between montelukast and placebo ( P = 0.10), but the montelukast group experienced an average 17% decrease in ICS dose and the control group experienced an average 64% increase in ICS dose. Conclusions Montelukast treatment significantly increased the number of rescue-free days in symptomatic children with asthma.
- Published
- 2003