首页> 外文期刊>Pediatric Pulmonology >Efficacy of once-daily versus twice-daily administration of budesonide by Turbuhaler(R) in children with stable asthma.
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Efficacy of once-daily versus twice-daily administration of budesonide by Turbuhaler(R) in children with stable asthma.

机译:Turbuhaler(R)对稳定型哮喘儿童每天一次布地奈德治疗与每天两次布地奈德治疗的疗效。

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We evaluated the efficacy of once-daily versus twice-daily treatment with budesonide, delivered by a Turbuhaler(R), in the management of children with stable asthma in a randomized, double-blind, parallel-group study involving 206 children (age 5-15 years). After a 2-week run-in period during which the children were maintained on their usual dose of budesonide (200 microg or 400 microg/day), patients were randomized to receive the same daily dose in either two daily administrations (morning and evening) or as a single dose in the morning over a period of 12 weeks. The primary efficacy variable was morning peak expiratory flow (PEF). The mean morning PEF during the run-in phase was 271 L/min in patients randomized to once-daily treatment and 264 L/min in those randomized to twice-daily treatment. The mean change from baseline to the last 2 weeks of the treatment period in the two groups was -0.3 L/min (95% confidence limits -6.6 to +6.0) and 2.5 L/min (-4.3 to +9.3). The estimated difference between the groups was -2.8 L/min, with 90% confidence limits of -10.4 + 4.5; these were close to the limits regarded as indicative of equivalence (-10 to +10), and hence the difference was not regarded as clinically relevant. Similarly, there were no significant differences between the groups in regard to secondary efficacy measures such as spirometric tests and symptom scores. Both treatments were well tolerated. We conclude that once-daily administration of budesonide by Turbuhaler(R) is as effective as twice-daily treatment in the management of stable asthma in children treated with inhaled steroids at doses of 200-400 microg/day. Copyright 1999 Wiley-Liss, Inc.
机译:在一项涉及206名儿童(年龄5岁)的随机,双盲,平行分组研究中,我们评估了由Turbuhaler(R)提供的布地奈德每日一次与每日两次治疗在稳定哮喘患儿管理中的疗效。 -15年)。在为期2周的磨合期后,在此期间,孩子们维持常规剂量的布地奈德(200微克或400微克/天),然后将患者随机分配为每天两次(早晨和晚上)服用相同的日剂量或在12周内的早晨以单剂量服用。主要功效变量是早晨峰值呼气流量(PEF)。随机分为每日一次治疗的患者在磨合期的平均早晨PEF为271 L / min,随机分为每天两次的患者为264 L / min。两组从基线到治疗期最后2周的平均变化为-0.3 L / min(95%置信度极限-6.6至+6.0)和2.5 L / min(-4.3至+9.3)。两组之间的估计差异为-2.8 L / min,90%置信限为-10.4 + 4.5;这些接近于被视为等同的极限(-10至+10),因此差异不被认为具有临床意义。同样,两组之间在二级功效测量(如肺活量测试和症状评分)方面也没有显着差异。两种治疗均耐受良好。我们得出的结论是,对于接受吸入类固醇治疗的儿童(剂量为200-400微克/天),每天一次布地奈德的治疗与稳定哮喘的治疗每天两次一样有效。版权所有1999 Wiley-Liss,Inc.

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