Ebden P, Jenkins A, Houston G, Davies B H
Thorax. 1986 Nov;41(11):869-74. doi: 10.1136/thx.41.11.869.
Twenty eight patients with chronic asthma took part in a double blind single crossover controlled trial of inhaled budesonide and inhaled beclomethasone dipropionate, using high doses of 1600 micrograms and 1500 micrograms daily respectively. Both drugs were administered by pressurised aerosol inhaler; the inhaler containing budesonide and its matching placebo were fitted with a collapsible spacer device. There was no significant difference in the control of asthma during the two six week treatment periods. There was no significant difference in FEV1 and forced vital capacity after four and six weeks of treatment or in mean morning and evening peak expiratory flow rates for the last 21 days of treatment. There was a small but statistically significant reduction in the daytime wheeze score while they were taking high dose budesonide but there was no difference for daytime activity, cough, and night symptoms. The mean basal cortisol concentrations were significantly lower after six weeks of high dose treatment than before treatment (budesonide p less than 0.01, beclomethasone p less than 0.05). There was no difference between mean basal cortisol values after six weeks of high dose treatment, and there was no effect on the rise of cortisol obtained after a short tetracosactrin test. High dose inhaled corticosteroids produced few side effects and were well tolerated.
28例慢性哮喘患者参与了一项吸入布地奈德和吸入丙酸倍氯米松的双盲单交叉对照试验,分别使用每日1600微克和1500微克的高剂量。两种药物均通过压力定量气雾剂吸入器给药;含有布地奈德的吸入器及其匹配的安慰剂均配备了可折叠的储物罐装置。在两个为期六周的治疗期内,哮喘控制情况无显著差异。治疗四周和六周后,第一秒用力呼气容积(FEV1)和用力肺活量无显著差异,治疗最后21天的平均早晚呼气峰值流速也无显著差异。在服用高剂量布地奈德期间,日间喘息评分有小幅但具有统计学意义的降低,但日间活动、咳嗽和夜间症状方面无差异。高剂量治疗六周后,平均基础皮质醇浓度显著低于治疗前(布地奈德p<0.01,丙酸倍氯米松p<0.05)。高剂量治疗六周后的平均基础皮质醇值之间无差异,且对短程二十四肽促皮质素试验后皮质醇的升高无影响。高剂量吸入糖皮质激素产生的副作用很少,耐受性良好。