Administration of budesonide once daily by means of turbuhaler to subjects with stable asthma.

Abstract

BACKGROUND:

Optimal management of chronic, mild-to-moderate asthma with inhaled steroids may include use of the lowest possible doses, as recommended in guidelines, and a reduction in the frequency of daily administration for greater convenience. Lower doses and once daily treatment with inhaled steroids must be rigorously evaluated in controlled clinical trials.

OBJECTIVES:

The objective of this study was to assess the efficacy and safety of once daily treatment with budesonide in subjects with stable asthma.

METHODS:

Once daily budesonide was assessed in 309 adult subjects, including those who were and were not using an inhaled steroid at baseline. The subjects were stratified by inhaled steroid use and randomly assigned to one of 3 treatments: 200 microgram budesonide, 400 microgram budesonide, or placebo administered by means of Turbuhaler once daily in the morning for 6 weeks. Beyond this point, treatment was continued unchanged for another 12 weeks (maintenance) in those receiving 200 microgram budesonide once daily and placebo. In those who received 400 microgram budesonide once daily, the dose was reduced to 200 microgram once daily at week 6 and held constant for the remaining 12 weeks (400/200 microgram group). Primary efficacy endpoints were mean change from baseline in FEV1 and morning peak expiratory flow.

RESULTS:

Once daily budesonide was well tolerated and resulted in significant improvements in all efficacy endpoints, even though baselines were well stabilized. Baseline lung function was elevated with little room for improvement; however, mean increases in FEV1 during the maintenance period were 0.10 L and 0.11 L in the 200 microgram and 400/200 microgram groups, respectively, versus a decrease of -0.09 L in the placebo arm (P <.001). Results for peak expiratory flow were similar. Significant improvements in secondary endpoints, including symptoms, beta-agonist use, and quality of life, also developed with budesonide 200 and 400 microgram once daily.

CONCLUSION:

Inhaled budesonide, in doses as low as 200 microgram, may be an appropriate introductory or maintenance dose in subjects with stable, mild-to-moderate asthma.

• Authors: E R McFadden, T B Casale, T B Edwards, J P Kemp, W J Metzger, H S Nelson, W W Storms, M J Neidl
• Journal: The Journal of allergy and clinical immunology (J Allergy Clin Immunol) Vol. 104 Issue 1 Pg. 46-52 (Jul 1999) ISSN: 0091-6749 [Print] United States
• PMID: 10400838 (Publication Type: Clinical Trial, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)

Chemical References

• Adrenergic beta-Agonists
• Anti-Inflammatory Agents
• Budesonide

Topics

• Administration, Inhalation
• Adolescent
• Adrenergic beta-Agonists (administration & dosage)
• Adult
• Aged
• Anti-Inflammatory Agents (administration & dosage, adverse effects)
• Asthma (drug therapy)
• Bronchial Spasm (chemically induced)
• Budesonide (administration & dosage, adverse effects)
• Dose-Response Relationship, Drug
• Double-Blind Method
• Female
• Headache (chemically induced)
• Humans
• Male
• Middle Aged
• Quality of Life
• Respiratory Function Tests
• Respiratory Tract Infections (chemically induced)