Abstract
The goal of the present study was to investigate the bronchodilating effects of 6 and 12 µg formoterol delivered by the Turbuhaler™, in comparison to salbutamol 200 µg (metered dose inhaler) and to controls without treatment. After inducing acute and severe bronchial obstruction by means of methacholine challenge, peak inspiratory mouth flow (PIMF) was measured through a stenosis, simulating the internal resistance of the Turbuhaler™, with the incheck ™ device. In addition the relationship was studied between PIMF and clinical response in the 3 treatment groups. In the 176 patients methacholine caused a mean fall in FEV1 of 37.1 ± 6.9% compared to baseline. Ten minutes after bronchodilator inhalation, FEV1 improved significantly in all three treatment groups. At 30 minutes after bronchodilator administration, only the salbutamol 200 µg and the formoterol 12 µg groups had a significantly greater increase in FEV1 than controls (0.69 ± 0.43 l and 0.66 ± 0.37 l vs 0.38 ± 0.32 l, p < 0.0005), whereas the formoterol 6 µg group showed no significant improvement (0.41 ± 0.38 l, p = 0.74). Thirteen patients (7.4%) did not reach a minimal PIMF of 30 l/min through the in-check™ device after challenge. In the four patients in the formoterol 6 µg group with a PIMF below 30 l/min inhalation did not cause bronchodilation. In conclusion, the results demonstrate that 6 µg formoterol via Turbuhaler™ leads to less and slower onset of bronchodilation compared to the other groups in our setting. If patients fail to generate a PIMF of 30 l/min, 6 µg formoterol via Turbuhaler™ may provide inadequate relief in a severe asthma attack.
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