Tolerance to bronchodilation is not overcome by high dose salbutamol

S. Haney, R. J. Hancox (Hamilton, New Zealand)

Source: Annual Congress 2005 - Bronchodilators with and without corticosteroids
Session: Bronchodilators with and without corticosteroids
Session type: Thematic Poster Session
Number: 839
Disease area: Airway diseases

Congress or journal article abstract

Abstract

Background: Asthmatics taking regular ß-agonists become tolerant to their bronchodilator effects. This is easily shown when bronchodilation is tested during a period of increased bronchomotor tone e.g. after methacholine challenge. Studies thus far have used up to 400μg of salbutamol. In clinical practice much higher doses are used to treat acute asthma. We tested the bronchodilator response to high-dose nebulised salbutamol in asthmatics taking regular formoterol.
Methods: Double-blind, placebo-controlled, crossover study. 11 adult asthmatics were randomised to formoterol 12μg twice daily or placebo for 1 week. 36 hours after the last dose, methacholine challenge was used to produce a 20% fall in FEV1. Salbutamol 5mg was then given by nebuliser and the FEV1 was measured over 20 minutes. Subjects then crossed over to the other medication. The main outcome measure was the area under the bronchodilator response curve (AUC). No additional ß-agonists were used throughout the study.
Results: The FEV1 and PD20 methacholine were not significantly different in the two arms. The response to salbutamol, assessed as AUC, was 18% lower after formoterol compared to placebo (95% confidence interval 0, 36%; p=0.03). The final FEV1 (20 minutes post-salbutamol) was also lower in the formoterol arm (2.67 vs 2.79L, 95% CI for difference 0.04, 0.20; p=0.05).
Conclusion: The bronchodilator response to salbutamol is reduced in subjects taking formoterol. This tolerance is not overcome by the use of high doses of nebulised salbutamol.
Supported by the Waikato Respiratory Research Fund.


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S. Haney, R. J. Hancox (Hamilton, New Zealand). Tolerance to bronchodilation is not overcome by high dose salbutamol. Eur Respir J 2005; 26: Suppl. 49, 839

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