The Division of Pediatric Clinical Pharmacology, National Jewish Health, Denver, Colo.
J Allergy Clin Immunol Pract. 2013 Jan;1(1):58-64. doi: 10.1016/j.jaip.2012.08.005. Epub 2012 Nov 8.
Budesonide inhalation suspension (BIS) and montelukast provide acceptable asthma control, whereas overall measures favored BIS in children aged 2 to 8 years with mild persistent asthma.
We compared BIS and montelukast over a 1-year period in children aged 2 to 4 years with asthma.
Data were derived from a 52-week, open-label, randomized, active-controlled, multicenter study (NCT00641472). Children with mild asthma received either BIS 0.5 mg or montelukast 4 to 5 mg once daily. Patients were stepped up to twice-daily BIS or oral corticosteroids for mild or severe asthma worsening, respectively. Primary efficacy assessment was time to first additional asthma medication for exacerbation over 52 weeks.
Two hundred two patients, age 2 to 4 years, received BIS (n = 105) or montelukast (n = 97). No difference was observed between the BIS and montelukast groups in median time to first additional asthma medication over 52 weeks (183 vs 86 days). Statistically significant differences were observed in favor of BIS over montelukast in the percentage of patients requiring oral steroids at 52 weeks (21.9% vs 37.1%; P = .022), the rate (number/patient/year) of additional courses of medication (1.35 vs 2.30; P = .003), the rate of additional oral steroid therapy (0.44 vs 0.88; P = .008), and caregivers' ability to manage the patient's symptoms (P = .026). Both treatments were well tolerated.
BIS and montelukast provided acceptable asthma control in children aged 2 to 4 years with mild persistent asthma with no significant difference between treatments in the primary end point; however, several secondary outcomes showed statistically significant differences (and many had numerical differences) in favor of BIS over montelukast.
布地奈德混悬液(BIS)和孟鲁司特均可实现良好的哮喘控制,然而,在 2 至 8 岁轻度持续性哮喘患儿中,总体措施更倾向于 BIS。
我们比较了 2 至 4 岁哮喘患儿使用 BIS 和孟鲁司特的 1 年疗效。
数据来源于一项为期 52 周、开放标签、随机、活性对照、多中心研究(NCT00641472)。轻度哮喘患儿接受 BIS 0.5mg 或孟鲁司特 4 至 5mg,每日一次。患儿分别因轻度或重度哮喘恶化而升级为每日两次 BIS 或口服皮质激素治疗。主要疗效评估是 52 周内首次因加重而使用额外哮喘药物的时间。
202 名年龄在 2 至 4 岁的患儿接受了 BIS(n=105)或孟鲁司特(n=97)治疗。在 52 周内首次因加重而使用额外哮喘药物的时间方面,BIS 组和孟鲁司特组之间无差异(中位数:183 天比 86 天)。BIS 在以下方面优于孟鲁司特:52 周时需要口服皮质激素的患者比例(21.9%比 37.1%;P=0.022)、药物附加疗程数(1.35 比 2.30;P=0.003)、附加口服皮质激素治疗率(0.44 比 0.88;P=0.008)和照护者管理患儿症状的能力(P=0.026)。两种治疗均耐受良好。
BIS 和孟鲁司特均可在 2 至 4 岁轻度持续性哮喘患儿中实现良好的哮喘控制,两种治疗在主要终点上无显著差异;然而,一些次要结局显示 BIS 优于孟鲁司特(在统计学上有显著差异,许多结局在数值上也有差异)。