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首页> 外文期刊>Annals of allergy, asthma, and immunology >Treatment with 400 microg of inhaled budesonide vs 200 microg of inhaled budesonide and oral montelukast in children with moderate persistent asthma: randomized controlled trial.
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Treatment with 400 microg of inhaled budesonide vs 200 microg of inhaled budesonide and oral montelukast in children with moderate persistent asthma: randomized controlled trial.

机译:中度持续性哮喘患儿用400 mg的布地奈德吸入治疗与200 mg的布地奈德吸入和口服孟鲁司特治疗:随机对照试验。

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BACKGROUND: Montelukast is reported to be beneficial in asthma as add-on therapy to inhaled corticosteroids and may reduce the need for the latter. OBJECTIVE: To evaluate whether a combination of oral montelukast and 200 microg of inhaled budesonide has comparable efficacy to 400 microg of inhaled budesonide alone in children with moderate persistent asthma. METHODS: In this prospective, blinded, hospital-based randomized controlled trial, 71 children with moderate persistent asthma were randomized to receive either montelukast, 5-mg chewable tablet, with 200 microg of inhaled budesonide or only 400 microg of inhaled budesonide daily for 12 weeks. Baseline and serial measurements of forced expiratory volume in 1 second, peak expiratory flow rate, and Asthma Symptom Score were performed; the frequency and severity of exacerbations were also recorded. RESULTS: Measurements of forced expiratory volume in 1 second, peak expiratory flow rate, and Asthma Symptom Score showed no significant differences between the 2 groups at baseline, during the serial follow-up visits, and at the end of the study. However, children who received montelukast had a greater frequency of exacerbations vs those who did not (33.3% vs 9.1%; P < .01). CONCLUSION: The overall control of asthma with 5 mg of oral montelukast and 200 microg of inhaled budesonide is inferior to that with 400 microg of inhaled budesonide in children with moderate persistent asthma.
机译:背景:据报道,孟鲁司特作为哮喘患者的吸入性皮质类固醇补充疗法对哮喘有益,并可能减少对后者的需求。目的:评估口服孟鲁司特和200微克布地奈德吸入剂对中度持续性哮喘患儿是否具有与仅400微克布地奈德吸入疗法相当的疗效。方法:在这项基于前瞻性,盲人,医院为基础的随机对照试验中,将71名患有中度持续性哮喘的儿童随机接受孟鲁司特,5毫克咀嚼片,每天200微克布地奈德吸入或仅400微克布地奈德吸入12次周。进行1秒内强制性呼气量,呼气峰值流速和哮喘症状评分的基线和系列测量;还记录了发作的频率和严重程度。结果:在1秒内的强制呼气量,呼气峰值流速和哮喘症状评分的测量结果显示,两组在基线,连续随访期间和研究结束时两组之间无显着差异。但是,接受孟鲁司特治疗的儿童与未接受孟鲁司特治疗的儿童相比,发作的频率更高(33.3%比9.1%; P <.01)。结论:中度持续性哮喘患儿口服5mg口服孟鲁司特和200μg吸入布地奈德对哮喘的总体控制效果不如400μg吸入布地奈德。

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