首页> 美国卫生研究院文献>Thorax >Corticosteroid trials in non-asthmatic chronic airflow obstruction: a comparison of oral prednisolone and inhaled beclomethasone dipropionate.
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Corticosteroid trials in non-asthmatic chronic airflow obstruction: a comparison of oral prednisolone and inhaled beclomethasone dipropionate.

机译:非哮喘慢性气流阻塞的皮质类固醇试验:口服泼尼松龙与吸入倍氯米松双丙酸酯的比较。

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摘要

One hundred and twenty seven adults considered on clinical grounds to have non-asthmatic chronic airflow obstruction entered a randomised, double blind, placebo controlled, crossover trial comparing the physiological response to inhaled beclomethasone dipropionate 500 micrograms thrice daily with oral prednisolone 40 mg a day, both given for two weeks. One hundred and seven patients completed the study. Response was assessed as change in FEV1 and FVC measured on the last treatment day, and as change in mean peak expiratory flow (PEF) over the final seven days of treatment from home PEF recordings performed five times daily. A full response to treatment was defined as an increase in FEV or FVC, or an increase in mean daily PEF over the final seven days of treatment, of at least 20% from baseline values. An improvement in one measurement of at least 15%, or of 10% in any two measurements, was defined as a partial treatment response. Response to placebo showed a significant order effect, suggesting a carry over effect of active treatment of at least three weeks. Response to active treatment was therefore related to initial baseline values, and compared with placebo by considering responses in the first treatment phase only. A full response to oral prednisolone (16/38) was significantly more common than to placebo (3/35). The number of full responses to inhaled beclomethasone (8/34) did not differ significantly from the number responding to oral prednisolone or placebo in the first treatment phase, though full and partial responses to inhaled beclomethasone (12/34) were significantly more common than those to placebo (4/35). When all three treatment phases were considered 44/107 patients showed a full response to one or both forms of corticosteroid treatment, a response to prednisolone (39) occurring more frequently than to inhaled beclomethasone (26). Only 21 of the 44 responders showed a response to both forms of treatment. Inhaled beclomethasone dipropionate 500 micrograms thrice daily was inferior to oral prednisolone 40 mg per day, but better than placebo, in producing improvement in physiological measurements in patients thought to have nonasthmatic chronic airflow obstruction. It was, however, an effective alternative in over half of those showing a response to prednisolone.
机译:127名因临床原因被认为患有非哮喘性慢性气流阻塞的成年人参加了一项随机,双盲,安慰剂对照,交叉试验,比较了每天吸入500 mg三次氯苯倍松酮和每天40 mg泼尼松龙的生理反应,都给了两个星期。一百零七名患者完成了研究。评估反应为在最后一个治疗日测量的FEV1和FVC的变化,以及每天进行五次家庭PEF记录的治疗的最后7天的平均最大呼气流量(PEF)的变化。对治疗的完全反应定义为在治疗的最后7天中FEV或FVC的增加,或平均每日PEF的增加,至少比基线值高20%。一项测量结果至少改善15%,或将任意两项测量结果改善10%定义为部分治疗反应。对安慰剂的反应显示出显着的有序效应,表明积极治疗至少三周的残留效应。因此,对积极治疗的反应与初始基线值有关,并且仅考虑第一个治疗阶段的反应就与安慰剂进行了比较。对口服泼尼松龙的完全缓解(16/38)比对安慰剂(3/35)的缓解更为普遍。在第一治疗阶段,对吸入的倍氯米松的完全反应(8/34)与对口服泼尼松龙或安慰剂的反应数量没有显着差异,尽管对吸入的倍氯米松(12/34)的完全和部分反应比安慰剂(4/35)。当考虑所有三个治疗阶段时,44/107例患者对一种或两种形式的皮质类固醇激素治疗均表现出完全反应,对泼尼松龙(39)的反应比对吸入倍氯米松(26)的反应更为频繁。在这44种反应者中,只有21种表现出对两种治疗方式的反应。每天吸入三次丙酸倍氯米松500微克,比口服泼尼松龙40毫克/天逊色,但优于安慰剂,在认为患有非哮喘性慢性气流阻塞的患者的生理指标方面有所改善。然而,在对泼尼松龙有反应的半数以上的患者中,它是一种有效的替代方法。

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