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Comparison of fluticasone propionate with beclomethasone dipropionate in moderate to severe asthma treated for one year. International Study Group.

机译:丙酸氟替卡松与丙酸倍氯米松治疗一年至中度哮喘的比较。国际研究小组。

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摘要

BACKGROUND--High dose inhaled glucocorticosteroids are increasingly used in the management of patients with moderate to severe asthma. Although effective, they may cause systemic side effects. Fluticasone propionate is a topically active inhaled glucocorticosteroid which has few systemic effects at high doses. METHODS--Fluticasone propionate, 1.5 mg per day, was compared with beclomethasone dipropionate at the same dose for one year in patients with symptomatic moderate to severe asthma; 142 patients received fluticasone propionate and 132 received beclomethasone dipropionate. The study was multicentre, double blind and of a parallel design. For the first three months patients attended the clinic every four weeks and completed daily diary cards. For the next nine months they were only seen at three monthly intervals in the clinic. RESULTS--During the first three months diary card peak expiratory flow (PEF) rate and lung function measurements in the clinic showed significantly greater improvement in patients receiving fluticasone propionate (difference in morning PEF 15 l/min (95% CI 6 to 25)), and these differences were apparent at the end of the first week. The improved lung function was maintained throughout the 12 month period and the number of severe exacerbations in patients receiving fluticasone propionate was reduced by 8% compared with those receiving beclomethasone dipropionate. No significant differences between the two groups were observed in morning plasma cortisol levels, urinary free cortisol levels, or response to synthetic ACTH stimulation. In addition, both the rates of withdrawal and of adverse events were low, and there were fewer exacerbations of asthma with fluticasone propionate than beclomethasone dipropionate. CONCLUSIONS--This study shows that fluticasone propionate in a daily dose of 1.5 mg results in a significantly greater increase in PEF and asthma control than the same dose of beclomethasone dipropionate, with no increase in systemic or other side effects.
机译:背景技术-高剂量吸入糖皮质激素已越来越多地用于中重度哮喘患者的治疗。尽管有效,但它们可能引起全身性副作用。丙酸氟替卡松是一种局部活性吸入糖皮质激素,在大剂量时几乎没有全身作用。方法:将有症状的中度至重度哮喘患者每天服用1.5 mg丙酸氟替卡松与相同剂量的倍氯米松双丙酸酯治疗一年。 142例患者接受丙酸氟替卡松,132例患者接受丙酸倍氯米松。该研究为多中心,双盲和平行设计。在头三个月中,患者每四个星期去诊所一次,并填写每日日记卡。在接下来的9个月里,他们仅隔三个月在诊所见过一次。结果-在头三个月的日记卡中,诊所的日记峰值呼气流量(PEF)率和肺功能测量显示丙酸氟替卡松患者的病情明显改善(早晨PEF差异为15 l / min(95%CI 6至25)) ),并且这些差异在第一周结束时就很明显。在整个12个月的时间内,肺功能一直保持改善,丙酸氟替卡松患者比丙酸倍氯米松患者严重加重次数减少了8%。两组的早晨血浆皮质醇水平,尿中游离皮质醇水平或对合成ACTH刺激的反应均未观察到明显差异。此外,停药和不良反应的发生率均较低,丙酸氟替卡松的哮喘发作加重率低于丙酸倍氯米松。结论-这项研究表明,与相同剂量的倍氯米松二丙酸酯相比,日剂量1.5毫克丙酸氟替卡松导致的PEF和哮喘控制明显增加,而全身或其他副作用没有增加。

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