Key result
Formoterol reduces bronchodilator response to salbutamol by ~48% versus placebo in asthma patients.
Why the study?
Regular use of beta-agonists leads to tolerance to their bronchodilator effects, but most studies assessed tolerance after beta-agonist withdrawal, not during ongoing treatment.
Does formoterol reduce the bronchodilator response to salbutamol in asthmatic subjects?
RCT (n=13)
Double-blind
Random-order
No
Does formoterol reduce the bronchodilator response to salbutamol in asthmatic subjects?
Mean Difference: 85.44 (95% CI 31.78–139.1)
Absolute Event Rate: 107% vs 205%
p-value: p=0.001
Treatment with the long-acting beta-agonist formoterol induces clinically relevant tolerance to the bronchodilator effects of rescue salbutamol in asthmatic patients.
Clinicians should anticipate reduced salbutamol rescue efficacy during LABA therapy; confirms tolerance develops without beta-agonist withdrawal in asthma.
BACKGROUND: Regular use of beta-agonists leads to tolerance to their bronchodilator effects. This can be demonstrated by measuring the response to beta-agonist following bronchoconstriction using methacholine. However most studies have demonstrated tolerance after a period of beta-agonist withdrawal, which is not typical of their use in clinical practice. This study assessed tolerance to the bronchodilator action of salbutamol during ongoing treatment with long-acting beta-agonist. METHODS: Random-order, double-blind, placebo-controlled, crossover trial. After 1 week without beta-agonists, 13 asthmatic subjects inhaled formoterol 12 microg twice daily or matching placebo for 1 week. Eight hours after the first and last doses subjects inhaled methacholine to produce a 20% fall in FEV1. Salbutamol 100, 200 and 400 microg (cumulative dose) was then given at 5-minute intervals and FEV1 was measured 5 minutes after each dose. After a 1 week washout subjects crossed over to the other treatment. Unscheduled use of beta-agonists was not allowed during the study. The main outcome variable was the area under the salbutamol response curve. RESULTS: The analysis showed a significant time by treatment interaction indicating that the response to salbutamol fell during formoterol therapy compared to placebo. After 1 week of formoterol the area under the salbutamol response curve was 48% (95% confidence interval 28 to 68%) lower than placebo. This reduction in response remained significant when the analyses were adjusted for changes in the pre-challenge FEV1 and dose of methacholine given (p = 0.001). CONCLUSION: The bronchodilator response to salbutamol is significantly reduced in patients taking formoterol. Clinically relevant tolerance to rescue beta-agonist treatment is likely to occur in patients treated with long-acting beta-agonists.
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Haney et al. (2005) conducted an RCT in Asthma (n=13). Formoterol vs. Placebo was evaluated on Area under the salbutamol response curve (AUC) expressed as a percentage of the methacholine-induced fall in FEV1 (MD 85.44, 95% CI 31.78-139.1, p=0.001). Formoterol treatment for 1 week significantly reduced the bronchodilator response to salbutamol by 48% compared to placebo in patients with asthma.
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