Malo J L, Cartier A, Merland N, Ghezzo H, Burek A, Morris J, Jennings B H
Department of Chest Medicine, Hopital du Sacré-Coeur, Montreal, Canada.
Am Rev Respir Dis. 1989 Sep;140(3):624-8. doi: 10.1164/ajrccm/140.3.624.
Fifty-three adult asthmatic subjects requiring 800 micrograms or more of inhaled beclomethasone dipropionate were enrolled in a double-blind parallel group study of 6-month duration to compare the efficacy and side effects of inhaled budesonide in doses of 800, 1,200, and 1,600 micrograms given two or four times a day (BID or QID). After a two-week observation period to establish baseline, subjects were given the same dose of budesonide as they would be for beclomethasone dipropionate; however, the frequency regimen (BID or QID) was randomly allocated. Subjects were asked to fill in diary cards describing their asthmatic symptoms, need for medication, and throat symptoms. They were assessed by a physician every 4 wk, at which time spirometry was performed. Throat swabs were done at every other monthly visit. Cortisol and response to cortisol after synthetic ACTH injection were assessed at the beginning and end of the trial. Thirty-six subjects, half in each group, completed the study. Those on the BID regimen had almost twice as many days with nocturnal asthma and cough and almost three times as many days with disability due to asthma. There were also twice as many relapses in the BID regimen as judged by the clinician. These relapses mainly occurred toward the end of the study. The maximal daily swings in peak expiratory flow rates were slightly greater in the BID group, although this difference was not physiologically significant. Spirometry, cortisol secretion, and the response after synthetic ACTH injection were not significantly different in either group from the beginning to the end of the study.(ABSTRACT TRUNCATED AT 250 WORDS)
五十三名需要吸入丙酸倍氯米松800微克或更多的成年哮喘患者参加了一项为期6个月的双盲平行组研究,以比较每日两次或四次(bid或QID)吸入800、1200和1600微克布地奈德的疗效和副作用。在经过两周的观察期以确定基线后,受试者接受与他们使用丙酸倍氯米松时相同剂量的布地奈德;然而,给药频率方案(bid或QID)是随机分配的。受试者被要求填写日记卡,描述他们的哮喘症状、用药需求和喉咙症状。每4周由医生对他们进行评估,此时进行肺功能测定。每隔一个月进行一次咽拭子检查。在试验开始和结束时评估皮质醇以及注射合成促肾上腺皮质激素后的皮质醇反应。三十六名受试者完成了研究,每组各有一半。采用bid给药方案的患者夜间哮喘和咳嗽的天数几乎是另一组的两倍,因哮喘导致残疾的天数几乎是另一组的三倍。根据临床医生的判断,bid给药方案的复发次数也是另一组的两倍。这些复发主要发生在研究接近尾声时。bid组的最大每日呼气峰值流速波动略大,尽管这种差异在生理上并不显著。从研究开始到结束,两组的肺功能测定、皮质醇分泌以及注射合成促肾上腺皮质激素后的反应均无显著差异。(摘要截短至250字)