Consultant Paediatrician, Royal Glamorgan Hospital, Llantrisant, Mid Glamorgan, Wales.
Clin Drug Investig. 2005;25(1):13-22. doi: 10.2165/00044011-200525010-00002.
To test the hypothesis that once-daily treatment with fluticasone propionate is as effective as twice-daily treatment in children with well controlled asthma.
Multicentre, randomised, double-blind, parallel-group study.
General practice, 86 UK centres.
328 children with a diagnosis of asthma and a mean age of 10 years (range 4-16 years), mean duration of asthma of 5.5 years, and a mean percentage predicted forced expiratory volume in 1 second prior to randomisation of 93% were randomised.
Patients entered a 4-week, open run-in period, receiving fluticasone propionate 50mug twice daily via a Diskustrade mark inhalation device. Patients whose asthma was well controlled according to predefined criteria were randomised to receive either fluticasone propionate 100mug at night and placebo in the morning (once daily [od] group; n = 151) or fluticasone propionate 50mug twice daily (bd) [bd group; n = 177] for 8 weeks.
Mean morning peak expiratory flow over the 8 weeks of treatment, recorded daily, adjusted for baseline, age, height and sex.
The 90% CI for the treatment difference in morning peak flow (bd-od) in the intention-to-treat population was -1.9 to 5.3 L/min, demonstrating clinical equivalence between bd and od administration. Fifteen patients withdrew from the study due to asthma-related problems, ten patients from the od group and five from the bd groups (p = 0.10). Both groups remained well controlled in terms of lung function, symptoms and use of relief medication throughout the study.
Once-daily treatment with fluticasone propionate 100mug at night is as effective as 50mug twice daily in children with well controlled mild-to-moderate asthma.
验证丙酸氟替卡松每日一次治疗与每日两次治疗在控制良好的哮喘儿童中的疗效相当这一假说。
多中心、随机、双盲、平行分组研究。
英国 86 个中心的普通诊所。
328 名被诊断为哮喘的儿童,平均年龄 10 岁(范围 4-16 岁),哮喘平均病程 5.5 年,随机分组前预测的 1 秒用力呼气量的平均百分比为 93%。
患者进入为期 4 周的开放性预试验期,通过 Diskustrade 吸入装置每日两次接受丙酸氟替卡松 50μg。根据预设标准,哮喘控制良好的患者被随机分为两组:一组在夜间接受丙酸氟替卡松 100μg 治疗,早晨接受安慰剂治疗(每日一次[od]组;n=151);另一组在夜间接受丙酸氟替卡松 50μg 治疗,早晨接受丙酸氟替卡松 50μg 治疗(bd 组;n=177),共治疗 8 周。
治疗 8 周期间的平均每日清晨呼气峰流速(PEF),经过基线、年龄、身高和性别调整后进行测量。
意向治疗人群中,清晨呼气峰流速(bd-od)的治疗差异的 90%可信区间为-1.9 至 5.3 L/min,表明 bd 和 od 给药具有临床等效性。由于哮喘相关问题,15 名患者退出研究,其中 10 名来自 od 组,5 名来自 bd 组(p=0.10)。在整个研究过程中,两组的肺功能、症状和缓解药物的使用均保持良好控制。
在控制良好的轻度至中度哮喘儿童中,每晚给予丙酸氟替卡松 100μg 一次治疗与每日两次 50μg 治疗同样有效。