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首页> 外文期刊>Advances in therapy. >Onset of bronchodilation with fluticasone/formoterol combination versus fluticasone/salmeterol in an open-label, randomized study.
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Onset of bronchodilation with fluticasone/formoterol combination versus fluticasone/salmeterol in an open-label, randomized study.

机译:在一项开放标签的随机研究中,与氟替卡松/沙美特罗联合使用氟替卡松/福莫特罗联合支气管扩张的发作。

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摘要

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.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.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).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.
机译:吸入的皮质类固醇,丙酸氟替卡松(fluticasone)和长效β(2)激动剂富马酸福莫特罗(formoterol)已合并在一个气雾剂吸入器中(fluticasone / formoterol)。在一项随机开放标签研究中,氟替卡松/福莫特罗在治疗12周后显示出与氟替卡松/沙美特罗相似的功效。这项事后分析比较了两种疗法与支气管扩张的发生。轻度至中度持续性哮喘的成人随机分为氟替卡松/福莫特罗(100/10或250/10μg,每日两次[出价])或氟替卡松/沙美特罗(100/50或250/50μg出价)持续12周。支气管扩张的发作(给药后的第一个时间点,即1秒内的强制呼气量[FEV(1)]大于给药前值≥12%),缓解率(达到支气管扩张的患者比例) ,并在第0天(基线)和第84天评估了FEV(1)的变化。在服药后的前120分钟内,氟替卡松/福莫特罗(n = 101)比氟替卡松/沙美特罗(n = 101)提供更快的支气管扩张作用。在第0天(危险比[HR] = 1.47 [95%CI 1.05-2.05])和84(HR = 1.77 [95%CI 1.14-2.73])。在第0天,服用氟替卡松/福莫特罗的患者在服药5分钟内达到支气管扩张的几率几乎是氟替卡松/沙美特罗的四倍(赔率[OR] = 3.97 [95%CI 1.96-8.03])和近10第84天时提高了3倍(或= 9.58 [95%CI 2.14-42.90]);服用氟替卡松/福莫特罗两天后,在服药后120分钟内达到支气管扩张的几率大约高出两倍。在第0天,使用氟替卡松/福莫特罗,在用药后120分钟内,最小二乘(LS)平均FEV1的总体增加百分比明显大于氟替卡松/沙美特罗(LS平均治疗差异:4.70%[95%CI 1.57- 7.83]; P = 0.003)和84(2.79%[95%CI 0.65-4.93]; P = 0.011)。这些分析表明,氟替卡松/福莫特罗起效比氟替卡松/沙美特罗起效快,维持了12周以上治疗。这种益处可以促进哮喘患者的治疗依从性。

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