Suppr超能文献

在一项开放性、随机研究中,与氟替卡松/沙美特罗相比,氟替卡松/福莫特罗联合治疗的支气管扩张作用起始时间。

Onset of bronchodilation with fluticasone/formoterol combination versus fluticasone/salmeterol in an open-label, randomized study.

机构信息

Department of Pulmonary Diseases, Martini Hospital, Groningen, Netherlands.

出版信息

Adv Ther. 2012 Nov;29(11):958-69. doi: 10.1007/s12325-012-0058-0. Epub 2012 Oct 17.

Abstract

INTRODUCTION

The inhaled corticosteroid, fluticasone propionate (fluticasone), and the long-acting beta(2)-agonist, formoterol fumarate (formoterol), have been combined in a single aerosol inhaler (fluticasone/formoterol). In a randomized, open-label study, fluticasone/formoterol showed similar efficacy to fluticasone/salmeterol after 12 weeks of treatment. This post-hoc analysis compared the onset of bronchodilation with the two treatments.

METHODS

Adults with mild-to-moderate-severe persistent asthma were randomized to fluticasone/formoterol (100/10 or 250/10 μg twice daily [b.i.d.]) or fluticasone/salmeterol (100/50 or 250/50 μg b.i.d.) for 12 weeks. The onset of bronchodilation (the first post-dose time point at which the forced expiratory volume in 1 second [FEV(1)] was ≥12% greater than the pre-dose value), responder rates (the proportion of patients achieving bronchodilation), and changes in FEV(1) were assessed at days 0 (baseline) and 84.

RESULTS

Fluticasone/formoterol (n = 101) provided more rapid onset of bronchodilation than fluticasone/salmeterol (n = 101) over the first 120 min post-dose on days 0 (hazard ratio [HR] = 1.47 [95% CI 1.05-2.05]) and 84 (HR = 1.77 [95% CI 1.14-2.73]). The odds of a patient achieving bronchodilation within 5 min of dosing were almost four-times higher with fluticasone/formoterol than with fluticasone/salmeterol on day 0 (odds ratio [OR] = 3.97 [95% CI 1.96-8.03]) and almost 10-times higher on day 84 (OR = 9.58 [95% CI 2.14-42.90]); the odds of achieving bronchodilation within 120 min post-dose were approximately twofold higher with fluticasone/formoterol on both days. The overall percentage increase in least-squares (LS) mean FEV1 during the 120-min post-dose period was significantly greater with fluticasone/formoterol than fluticasone/salmeterol on days 0 (LS mean treatment difference: 4.70% [95% CI 1.57-7.83]; P = 0.003) and 84 (2.79% [95% CI 0.65-4.93]; P = 0.011).

CONCLUSION

These analyses showed that fluticasone/formoterol provided a faster onset of bronchodilation than fluticasone/salmeterol, which was maintained over 12 weeks of treatment. This benefit may facilitate treatment adherence among patients with asthma.

摘要

简介

吸入性皮质类固醇药物丙酸氟替卡松(fluticasone)和长效β2-激动剂富马酸福莫特罗(formoterol)已被合并在一种单一的气雾剂吸入器(fluticasone/formoterol)中。在一项随机、开放性研究中,fluticasone/formoterol 在治疗 12 周后显示出与 fluticasone/salmeterol 相似的疗效。这项事后分析比较了两种治疗方法的支气管扩张起始时间。

方法

轻度至中度重度持续性哮喘患者被随机分配接受丙酸氟替卡松/福莫特罗(100/10 或 250/10 μg,每日两次[bid.])或丙酸氟替卡松/沙美特罗(100/50 或 250/50 μg,bid.])治疗 12 周。支气管扩张的起始时间(第一次给药后用力呼气量 1 秒[FEV(1)]比给药前增加≥12%的时间点)、应答率(达到支气管扩张的患者比例)以及 FEV(1)的变化在第 0 天(基线)和第 84 天进行评估。

结果

在第 0 天(HR = 1.47 [95% CI 1.05-2.05])和第 84 天(HR = 1.77 [95% CI 1.14-2.73]),与 fluticasone/salmeterol 相比,fluticasone/formoterol 在给药后 120 分钟内更快地引起支气管扩张。与 fluticasone/salmeterol 相比,fluticasone/formoterol 在第 0 天达到支气管扩张的患者比例在 5 分钟内达到治疗效果的可能性几乎高出四倍(优势比[OR] = 3.97 [95% CI 1.96-8.03]),在第 84 天达到支气管扩张的患者比例高出近 10 倍(OR = 9.58 [95% CI 2.14-42.90]);fluticasone/formoterol 在这两天内达到支气管扩张的可能性在给药后 120 分钟内增加了约两倍。在给药后 120 分钟期间,最小二乘(LS)平均 FEV1 的总体百分比增加,fluticasone/formoterol 明显优于 fluticasone/salmeterol,第 0 天(LS 平均治疗差异:4.70% [95% CI 1.57-7.83];P = 0.003) 和第 84 天(2.79% [95% CI 0.65-4.93];P = 0.011)。

结论

这些分析表明,fluticasone/formoterol 比 fluticasone/salmeterol 更快地引起支气管扩张,并且在 12 周的治疗期间保持稳定。这种益处可能有助于提高哮喘患者的治疗依从性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验