Bundgaard A, Schmidt A
Eur J Respir Dis Suppl. 1983;130:66-72.
Eighteen adult asthmatics participated in a placebo controlled, double-blind, randomised study comparing the efficacy of pretreatment with fenoterol administered by pressurized aerosol and as a dry powder on exercise-induced asthma. The dosages used were 0.6 mg and 1.0 mg as both pressurized aerosol and dry powder. The pretreatment was given over a period of 10 min. Six min of treadmill-running was performed in a climate chamber 30 min after pretreatment on five successive days. The lung function was assessed by peak expiratory rate. The decrease in lung function following pretreatment with placebo was 32% (average +/- (SEM) (2). Falls of 9% (2) and 8% (1) were seen after pretreatment with 0.6 and 1.0 mg from a pressurized aerosol. The falls following pretreatment with 0.6 and 1.0 mg of dry powder were 8% (2) and 8%, respectively. It is concluded that pretreatment of exercise-induced asthma with a beta-2-agonist is equally effective whether dosed from a pressurized aerosol as when given as a dry powder. A dose of 0.6 mg is just as effective as a dose of 1.0 mg when inhaled over a period of ten min.
18名成年哮喘患者参与了一项安慰剂对照、双盲、随机研究,比较了使用压力定量气雾剂和干粉吸入的非诺特罗预处理对运动诱发性哮喘的疗效。压力定量气雾剂和干粉吸入的使用剂量均为0.6毫克和1.0毫克。预处理持续10分钟。在预处理30分钟后,在气候舱内连续五天每天进行6分钟的跑步机跑步。通过呼气峰值速率评估肺功能。安慰剂预处理后肺功能下降32%(平均±(标准误)(2))。压力定量气雾剂0.6毫克和1.0毫克预处理后肺功能分别下降9%(2)和8%(1)。干粉0.6毫克和1.0毫克预处理后肺功能下降分别为8%(2)和8%。结论是,β2激动剂预处理运动诱发性哮喘,无论是通过压力定量气雾剂给药还是干粉给药,效果相同。吸入十分钟时,0.6毫克剂量与1.0毫克剂量效果相同。