Conclusion During sleep lung mucociliary clearance in stable asthma was reduced, which is in agreement with the group's previous findings. Treatment with controlled/slow release oral bronchodilators had no effect on this reduced rate of clearance associated with sleep. (Thorax 1993;48:287-289) Lung mucociliary clearance, one of the lung's host defence clearance mechanisms, is impaired in patients with airways disease.1-4 Furthermore, lung mucociliary clearance has been shown to be reduced during sleep in healthy subjects5 and in patients with asthma,6 and this may contribute to the mucus plugging which is known to be present in the small airways of asthma sufferers.7Tracheobronchial clearance rates have been shown to be enhanced by /32 adrenergic drugs and methylxanthines.A-1 Oral slow release bronchodilators are often prescribed to patients to treat nocturnal asthma. We report a study in patients with asthma to compare the effects of controlled release salbutamol (Volmax, a /32 agonist), theophylline (Phyllocontin Forte Continus, a methylxanthine), and placebo on overnight changes in lung mucociliary clearance.
Methods
PATIENTSTwelve patients with asthma, six of whom were male, volunteered for the study. Three (two female) were withdrawn, two because of an exacerbation of their asthma (one during the run in period and the other during the salbutamol period), and the third because he was unable to manage without an oral bronchodilator during the run in period.The patients who completed the study had a mean(SE) age of 65(5) years, percentage predicted FEV, of 61(9)% and a tobacco consumption of 12(5) pack years (seven exsmokers and two non-smokers). Seven patients were receiving treatment with inhaled /32 agonists and corticosteroids, three of whom were taking inhaled anticholinergic drugs. One other patient was receiving inhaled sodium cromoglycate only. The ninth patient was on no medication. Five of the patients were also receiving treatment with oral bronchodilators (four methylxanthines and one a /32 agonist), which were discontinued for the one week run in period and for the duration of the trial. All nine patients had shown a 15% or greater reversibility of FEV, following the inhalation of 200 ,ug salbutamol (n = 5), or a 20% or greater difference between the maximum and minimum peak expiratory flows (PEF) obtained for that day on at least two days where the PEF had been measured on seven consecutive days (n = 6), or both.STUDY DESIGN Salbutamol (8 mg twice daily), theophylline (350 mg twice daily) and placebo tablets were compared in a double blind, randomised, crossover study of seven weeks' duration. Patients underwent a one week run in period followed by three treatment periods, each of two weeks, which were not separated by wash 287 on 11 May 2018 by guest. Protected by copyright.