首页> 外文期刊>Chest: The Journal of Circulation, Respiration and Related Systems >Comparison of the effect of low-dose ciclesonide and fixed-dose fluticasone propionate and salmeterol combination on long-term asthma control.
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Comparison of the effect of low-dose ciclesonide and fixed-dose fluticasone propionate and salmeterol combination on long-term asthma control.

机译:小剂量克索奈德和固定剂量丙酸氟替卡松联合沙美特罗治疗长期哮喘的效果比较。

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BACKGROUND: Patients with mild persistent asthma constitute about 70% of the asthma population; thus, it is important to know which first-line treatment is best for the management of mild asthma. We compared benefits of first-line treatment with ciclesonide and a combination of fluticasone and salmeterol in patients with mild asthma. METHODS: Patients aged 12 to 75 years with mild persistent asthma were enrolled in a randomized, double-blind, placebo-controlled study. After run-in, patients were randomized to ciclesonide 160 mug once daily (CIC160), fluticasone propionate/salmeterol 100/50 mug bid (FP200/S100), or placebo for 52 weeks. The primary variable was time to first severe asthma exacerbation; the coprimary variable was the percentage of poorly controlled asthma days. Patients recorded asthma symptoms and salbutamol use in electronic diaries and completed a standardized version of the Asthma Quality of Life Questionnaire. RESULTS: Compared with placebo, the time to first severe asthma exacerbation was prolonged, and lung function was improved with FP200/S100 treatment (P = .0002) but not with CIC160. Both CIC160 and FP200/S100 provided significantly fewer poorly controlled asthma days than placebo (P
机译:背景:轻度持续性哮喘患者约占哮喘人口的70%。因此,重要的是要知道哪种一线治疗最适合控制轻度哮喘。我们比较了在轻度哮喘患者中使用克索奈德以及氟替卡松和沙美特罗联合治疗的一线治疗的益处。方法:将12至75岁的轻度持续性哮喘患者纳入一项随机,双盲,安慰剂对照研究。磨合后,患者被随机分配至ciclesonide 160马克杯(CIC160),丙酸氟替卡松/沙美特罗100/50马克杯(FP200 / S100)或安慰剂,持续52周。主要变量是首次开始严重哮喘发作的时间。主要变量是哮喘控制天数差的百分比。患者在电子日记中记录了哮喘症状和沙丁胺醇使用情况,并完成了哮喘生活质量问卷的标准化版本。结果:与安慰剂相比,FP200 / S100治疗可延长首次严重哮喘发作的时间,并改善肺功能(P = .0002),而CIC160则不能。与安慰剂相比,CIC160和FP200 / S100所提供的哮喘控制天数均明显少于安慰剂(两种有效疗法的P均= .0016)。此外,两种有效疗法均显着增加了无哮喘症状天数(P

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