首页> 外文期刊>Clinical drug investigation >Salmeterol/Fluticasone Propionate via Diskus? Once Daily versus Fluticasone Propionate Twice Daily in Patients with Mild Asthma not Previously Receiving Maintenance Corticosteroids
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Salmeterol/Fluticasone Propionate via Diskus? Once Daily versus Fluticasone Propionate Twice Daily in Patients with Mild Asthma not Previously Receiving Maintenance Corticosteroids

机译:通过Diskus的沙美特罗/丙酸氟替卡松吗?未曾接受维持性糖皮质激素治疗的轻度哮喘患者每天一次,丙酸氟替卡松两次

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Background and objective: The efficacy and safety of twice-daily inhaled salmeterol/fluticasone propionate combination (SFC) therapy have been well established in the treatment of adults and adolescents with asthma. Once-daily administration of SFC could also be appropriate in patients with mild persistent asthma. This study aimed to investigate whether once-daily SFC 50 mug/100 mug was at least as effective as fluticasone propionate (FP) 100 mug twice daily, and more effective than twice-daily placebo, over 52 weeks as initial maintenance therapy in patients with mild persistent asthma. Methods: This was a randomized, double-blind, double-dummy, placebo-controlled, multicentre, parallel-group study carried out in primary and secondary care. Patients aged between 12 and 79 years with a documented clinical history of asthma for >=6 months who were currently receiving inhaled short-acting beta_2-adre-noceptor agonists only were enrolled. Patients were randomized to receive either once-daily inhaled SFC 50 mug/100 mug, twice-daily inhaled FP 100 mug (i.e. twice the dose of FP compared with SFC) or placebo for 52 weeks. The primary efficacy endpoints were mean morning peak expiratory flow (PEF), as recorded by patients prior to the use of bronchodilator or study medication, and the rate of investigator-recorded asthma exacerbations. Results: Patients receiving twice-daily FP and once-daily SFC showed greater improvements in mean morning PEF compared with those receiving placebo (FP, difference in means 20.1 L/min; 95% CI 14.7, 25.5; p < 0.001; SFC, difference in means 14.8 L/min; 95% CI 9.4, 20.2; p < 0.001). The difference in adjusted mean PEF between once-daily SFC and twice-daily FP was -5.3 L/min (95% CI -9.1, -1.6). PEF results showed that once-daily SFC was non-inferior to twice-daily FP. Over 52 weeks, there was a 35% reduction in exacerbation rates with once-daily SFC, which in this respect demonstrated superiority over placebo (p < 0.001). Non-inferiority between once-daily SFC and twice-daily FP with respect to exacerbation rates was not shown. Once-daily SFC significantly improved clinic forced expiratory flow between 25% and 75% of forced vital capacity (difference in means 0.129 L/s; p < 0.001) and clinic PEF (difference in means 10.8 L/min; p < 0.001) compared with twice-daily FP. Both treatments were well tolerated and the safety profile of each was similar to that seen with placebo. Conclusion: In patients with mild persistent asthma not previously receiving maintenance therapy, once-daily SFC 50 mug/100 mug is an effective treatment compared with placebo, and was non-inferior to twice-daily FP 100 mug with respect to mean morning PEF. However, in this study, once-daily SFC was not as efficacious as twice-daily FP in reducing asthma exacerbation rates. This study confirms the benefits of regular maintenance treatment in patients with mild persistent asthma.
机译:背景与目的:每天两次吸入沙美特罗/丙酸氟替卡松联合(SFC)疗法在成人和青少年哮喘治疗中的疗效和安全性已经确立。对于轻度持续性哮喘患者,每天一次给予SFC也可能是合适的。这项研究旨在调查在52周内,每天两次SFC 50杯/ 100杯作为初次维持治疗在52周内是否至少与丙酸氟替卡松(FP)100杯一样有效,并且比每日两次安慰剂更有效。轻度持续性哮喘。方法:这是一项在初级和二级保健中进行的随机,双盲,双盲,安慰剂对照,多中心,平行组研究。纳入年龄在12至79岁之间且有哮喘的临床病史且≥6个月的患者,这些患者目前仅接受吸入的短效β_2-肾上腺素受体激动剂。患者随机接受52周的每日一次吸入SFC 50杯/ 100杯,每天两次吸入FP 100杯(即,FP的剂量是SFC的两倍)或安慰剂,共52周。主要疗效终点是使用支气管扩张剂或研究药物之前患者记录的平均早晨峰值呼气流量(PEF),以及研究者记录的哮喘急性发作率。结果:与接受安慰剂的患者相比,接受每日两次FP和每天一次SFC的患者的平均早晨PEF改善更大(FP,均值差异为20.1 L / min; 95%CI为14.7,25.5; p <0.001; SFC,差异平均值14.8 L / min; 95%CI 9.4,20.2; p <0.001)。每日一次SFC和每天两次FP之间的调整后平均PEF差异为-5.3 L / min(95%CI -9.1,-1.6)。 PEF结果显示,每天一次的SFC不亚于每天两次的FP。在52周内,每天使用一次SFC可使病情恶化率降低35%,在这方面,它显示出优于安慰剂的治疗效果(p <0.001)。没有显示每天一次SFC和每天两次FP在恶化率方面的非劣效性。每天一次的SFC显着改善了诊所强制呼气流量,介于强制肺活量的25%至75%之间(均值差异为0.129 L / s; p <0.001)和诊所PEF(均值差异为10.8 L / min; p <0.001)每天两次使用FP。两种疗法的耐受性都很好,每种疗法的安全性与安慰剂相似。结论:对于先前未接受维持治疗的轻度持续性哮喘患者,每天一次SFC 50杯/ 100杯与安慰剂相比是一种有效的治疗方法,相对于平均早晨PEF,其效果不逊于每天两次FP 100杯。但是,在这项研究中,每天一次的SFC在降低哮喘急性发作率方面不如每天两次的FP有效。这项研究证实了定期维持治疗对轻度持续性哮喘患者的益处。

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