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非哮喘性慢性气流受限患者的皮质类固醇试验:口服泼尼松龙与吸入丙酸倍氯米松的比较

Corticosteroid trials in non-asthmatic chronic airflow obstruction: a comparison of oral prednisolone and inhaled beclomethasone dipropionate.

作者信息

Weir D C, Gove R I, Robertson A S, Burge P S

机构信息

Department of Thoracic Medicine, East Birmingham Hospital.

出版信息

Thorax. 1990 Feb;45(2):112-7. doi: 10.1136/thx.45.2.112.

Abstract

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.

摘要

127名临床上被认为患有非哮喘性慢性气流阻塞的成年人进入了一项随机、双盲、安慰剂对照的交叉试验,比较每日三次吸入500微克丙酸倍氯米松与每日口服40毫克泼尼松龙的生理反应,两种治疗均持续两周。107名患者完成了研究。通过测量最后治疗日的FEV1和FVC变化,以及根据治疗最后七天每日五次家庭PEF记录得出的平均呼气峰值流速(PEF)变化来评估反应。对治疗的完全反应定义为FEV或FVC增加,或治疗最后七天的平均每日PEF较基线值增加至少20%。一项测量至少改善15%,或任意两项测量改善10%,被定义为部分治疗反应。对安慰剂的反应显示出显著的顺序效应,提示活性治疗的残留效应至少持续三周。因此,对活性治疗的反应与初始基线值相关,并且仅通过考虑第一个治疗阶段的反应与安慰剂进行比较。对口服泼尼松龙的完全反应(16/38)显著多于对安慰剂的反应(3/35)。吸入丙酸倍氯米松的完全反应数量(8/34)在第一个治疗阶段与口服泼尼松龙或安慰剂的反应数量相比无显著差异,尽管吸入丙酸倍氯米松的完全和部分反应(12/34)显著多于对安慰剂的反应(4/35)。当考虑所有三个治疗阶段时,107名患者中有44名对一种或两种形式的皮质类固醇治疗表现出完全反应,对泼尼松龙的反应(39例)比对吸入丙酸倍氯米松的反应(26例)更频繁。44名反应者中只有21名对两种治疗形式均有反应。对于被认为患有非哮喘性慢性气流阻塞的患者,每日三次吸入500微克丙酸倍氯米松在改善生理测量指标方面不如每日口服40毫克泼尼松龙,但优于安慰剂。然而,在对泼尼松龙有反应的患者中,超过一半的患者使用它是一种有效的替代方法。

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