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Published on: November 4, 2010
Comparison of ipratropium solution, fenoterol solution, and their combination administered by nebulizer and face mask
W T Watson1, A B Becker, F E Simons
1Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, Canada.
Insights
The combination of ipratropium bromide and fenoterol hydrobromide significantly improved lung function in children with acute asthma. This dual therapy showed greater benefits than either bronchodilator alone, with no adverse effects reported.
Area of Science:
- Pediatric Pulmonology
- Respiratory Medicine
- Clinical Pharmacology
Background:
- Acute asthma exacerbations in children require effective bronchodilator therapy.
- Inhaled short-acting beta-agonists and anticholinergics are commonly used.
- Optimizing combination therapy for acute pediatric asthma is crucial.
Purpose of the Study:
- To compare the efficacy of ipratropium/fenoterol combination versus monotherapy in children with acute asthma.
- To evaluate the impact on pulmonary function, clinical scores, and oxygen saturation.
Main Methods:
- Randomized, double-blind, parallel-group trial with 47 children.
- Three treatment arms: ipratropium/fenoterol, fenoterol alone, ipratropium alone.
- Nebulizer administration with repeat dose; monitoring at 30, 60, 90, 120 minutes.
Main Results:
- All groups showed significant clinical score improvement.
- Ipratropium/fenoterol demonstrated the greatest improvement in FEV1 (forced expiratory volume in 1 second).
- Combination therapy was superior to fenoterol alone for percent change in FEV1 and to ipratropium alone for mid/low lung volume flow.
Conclusions:
- Ipratropium/fenoterol combination is an effective treatment for acute asthma in children.
- This combination offers superior bronchodilation compared to monotherapy.
- The treatment was well-tolerated with no significant adverse events.
Abstract:
In a randomized, double-blind, parallel-group trial, 47 children with acute asthma received a combination of ipratropium bromide solution (250 micrograms) and fenoterol hydrobromide solution (625 micrograms), fenoterol solution (625 micrograms) alone, or ipratropium solution (250 micrograms) alone, administered by face mask and nebulizer, with the dose repeated 60 minutes later. The groups did not differ significantly with regard to age, pulmonary function at baseline, or any other variable. They were monitored at 30, 60, 90, and 120 minutes by use of a clinical score, oxygen saturation, and pulmonary function tests. At the end of the study, albuterol was administered to assess residual bronchoconstriction. Clinical scores improved significantly after treatment in all groups at all times compared with baseline. The greatest improvement in FEV1 was seen in the patients treated with ipratropium/fenoterol, whether considered as absolute change, change in percent predicted, or percent change from baseline. Ipratropium/fenoterol was significantly better than fenoterol alone only when considered as percent change from baseline. Improvement in flow at mid and low lung volumes was significantly greater for the ipratropium/fenoterol combination than for ipratropium alone; no significant differences were noted between ipratropium/fenoterol and fenoterol for flow at mid and low lung volumes. Treatment with albuterol did not significantly improve pulmonary function in the groups receiving ipratropium/fenoterol or fenoterol alone, but it did increase flow at all lung volumes in the group receiving ipratropium alone. No patient complained spontaneously of any adverse reactions, and no clinically significant changes in heart rate or systolic or diastolic blood pressures occurred.(ABSTRACT TRUNCATED AT 250 WORDS)
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