Stanford Richard H, Shah Manan, Chaudhari Sham L
GlaxoSmithKline, Research Triangle Park, North Carolina, USA.
Open Respir Med J. 2012;6:37-43. doi: 10.2174/1874306401206010037. Epub 2012 Jun 21.
Inhaled corticosteroids (ICS) are preferred first-line controller agents for adults and adolescents with asthma. There is limited effectiveness data comparing ICS to leukotriene receptor antagonists (LTRA) in children with asthma aged 4 to 11 years.
A retrospective, matched cohort study was conducted using medical and pharmacy claims data. Asthma patients (ICD-9, 493.xx) naïve to any asthma controller therapy, and having ≥1 dispensing of fluticasone propionate 44 mcg (FP44), an ICS, or montelukast any dose (MON), an LTRA, were identified. Drug cohorts were matched (1:2) using propensity scores. Outcomes during follow-up included asthma-related ED visits, composite measure of asthma-related ED/hospital visit, asthma-related costs per month, and monthly rescue medication use. Statistical differences between cohorts were evaluated using multivariate regression models.
The final matched sample included 6,636 patients (FP44=2,212; MON=4,424). During follow-up, the FP44 cohort had a 29% significantly lower risk of an asthma-related ED visit (Hazard ratio (95% CI) =0.71 (0.52, 0.96)) compared to the MON cohort. Monthly asthma-related costs were significantly reduced on average by 36% in the FP44 compared to the MON cohort ($48 vs $75, p<0.05). Use of short-acting beta-agonists per month were similar between cohorts but monthly adjusted number of oral corticosteroid prescriptions were significantly lower in the FP44 compared to the MON cohort (0.03 vs 0.04, p<0.001).
Initiation of FP44 versus MON in children with asthma aged 4 to 11 years is associated with a significant reduction in asthma-related ED visits, costs, and oral corticosteroid use.
吸入性糖皮质激素(ICS)是成人和青少年哮喘患者首选的一线控制药物。在4至11岁哮喘儿童中,将ICS与白三烯受体拮抗剂(LTRA)进行疗效比较的数据有限。
利用医疗和药房报销数据进行了一项回顾性匹配队列研究。纳入对任何哮喘控制治疗均未用过且有≥1次丙酸氟替卡松44 mcg(FP44,一种ICS)或任何剂量孟鲁司特(MON,一种LTRA)配药记录的哮喘患者(ICD-9编码为493.xx)。使用倾向得分将药物队列进行1:2匹配。随访期间的结局包括与哮喘相关的急诊就诊、与哮喘相关的急诊/住院就诊综合指标、每月哮喘相关费用以及每月急救药物使用情况。使用多变量回归模型评估队列之间的统计学差异。
最终匹配样本包括6636例患者(FP44组=2212例;MON组=4424例)。随访期间,与MON组相比,FP44组发生与哮喘相关急诊就诊的风险显著降低29%(风险比(95%置信区间)=0.71(0.52,0.96))。与MON组相比,FP44组每月哮喘相关费用平均显著降低36%(48美元对75美元,p<0.05)。两组每月短效β受体激动剂的使用情况相似,但与MON组相比,FP44组每月口服糖皮质激素处方的调整数量显著更低(0.03对0.04,p<0.001)。
4至11岁哮喘儿童起始使用FP44而非MON与哮喘相关急诊就诊、费用及口服糖皮质激素使用的显著减少相关。