Pearlman David, Qaqundah Paul, Matz Jonathan, Yancey Steven W, Stempel David A, Ortega Hector G
Colorado Allergy and Asthma Centers, PC, Denver, Colorado, USA.
Pediatr Pulmonol. 2009 May;44(5):429-35. doi: 10.1002/ppul.20962.
Exercise is a common trigger in children with persistent asthma and inhaled corticosteroids have been shown to effectively treat clinical manifestations of persistent asthma, including protection from decrements in lung function caused by exercise. The goal of this study was to evaluate the effectiveness of fluticasone propionate/salmeterol 100/50 mcg compared with fluticasone propionate 100 mcg for the prevention of airflow limitation triggered by standardized exercise challenge in pediatric and adolescent patients with persistent asthma.
Multicenter, randomized, double-blind, parallel group trial of 248 subjects with persistent asthma (age 4-17 years) randomized to receive fluticasone propionate/salmeterol (100/50 mcg twice daily) or fluticasone propionate alone (100 mcg twice daily) via Diskus for 4 weeks. Exercise challenge tests were performed during screening and approximately 8 hr after administration of the blinded study medication on Treatment Day 28.
After 4 weeks of therapy both treatments provided protection following exercise challenge. The protection estimated by the maximal fall in FEV(1) was significantly better for fluticasone propionate/salmeterol (9.5 +/- 0.8% [mean +/- SE]) compared with fluticasone propionate alone (12.7 +/- 1.1%, P = 0.021). Statistically significant differences were not observed for asthma rescue-free days and asthma symptom-free days.
Chronic dosing with fluticasone propionate/salmeterol in a single device provides superior protection compared with an inhaled corticosteroid alone in protecting against exercise-induced asthma in children with persistent asthma.
运动是持续性哮喘患儿常见的诱发因素,吸入性糖皮质激素已被证明可有效治疗持续性哮喘的临床表现,包括预防运动引起的肺功能下降。本研究的目的是评估丙酸氟替卡松/沙美特罗100/50微克与丙酸氟替卡松100微克相比,在预防持续性哮喘儿童和青少年患者标准化运动激发试验引发的气流受限方面的有效性。
对248名持续性哮喘患者(4至17岁)进行多中心、随机、双盲、平行组试验,随机分为接受丙酸氟替卡松/沙美特罗(每日两次,每次100/50微克)或单独使用丙酸氟替卡松(每日两次,每次100微克),通过都保吸入4周。在筛查期间以及治疗第28天给予盲法研究药物后约8小时进行运动激发试验。
治疗4周后,两种治疗在运动激发试验后均提供了保护。与单独使用丙酸氟替卡松(12.7±1.1%)相比,丙酸氟替卡松/沙美特罗(9.5±0.8%[平均值±标准误])通过FEV(1)的最大下降估计的保护效果显著更好(P = 0.021)。在无哮喘急救天数和无哮喘症状天数方面未观察到统计学上的显著差异。
与单独使用吸入性糖皮质激素相比,在单一装置中慢性给予丙酸氟替卡松/沙美特罗在预防持续性哮喘儿童运动诱发哮喘方面提供了更好的保护。