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首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Adherence to inhaled corticosteroids: An ancillary study of the Childhood Asthma Management Program clinical trial
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Adherence to inhaled corticosteroids: An ancillary study of the Childhood Asthma Management Program clinical trial

机译:坚持吸入糖皮质激素:儿童哮喘管理计划临床试验的一项辅助研究

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Background: Information comparing subjective and objective measurements of adherence to study medications and the effects of adherence on treatment-related differences in asthma clinical trials are limited. Objective: We sought to compare subjective and objective measurements of children's adherence to inhaled corticosteroids or placebo and to determine whether adherence to study medications modified treatment-related differences in outcomes. Methods: In an ancillary study conducted in 3 of 8 Childhood Asthma Management Program Clinical Centers, adherence was assessed by using self-reported and objective data in 5- to 12-year-old children with mild or moderate asthma who were randomly assigned to 200 μg of inhaled budesonide twice per day (n = 84) or placebo (n = 56) for 4 years. The κ statistic was used to evaluate agreement between self-reported adherence (daily diary cards) and objectively measured adherence (number of doses left in study inhalers). Multivariable analyses were used to determine whether adherence to study treatment modified treatment-related differences in outcomes. Results: Adherence of less than 80% was seen in 75% of 140 children when adherence was measured objectively but only in 6% of children when measured by means of self-report. There was poor agreement between objective and subjective measurements of adherence of at least 80% (κ = 0.00; 95% CI, -0.05 to 0.04); self-reported adherence over the 4-year period generally overestimated objectively measured adherence (93.6% vs 60.8%, P <.0001). There was little evidence to indicate that adherence modified treatment-related differences in outcomes. Conclusion: Researchers should use objective rather than self-reported adherence data to identify clinical trial participants with low levels of adherence to study treatment.
机译:背景:在哮喘临床试验中,比较对研究药物依从性的主观和客观测量以及依从性对治疗相关差异的影响的信息有限。目的:我们试图比较儿童对吸入性糖皮质激素或安慰剂依从性的主观和客观测量,并确定依从性研究药物是否可改善治疗相关的结局差异。方法:在8个儿童哮喘管理计划临床中心中的3个中进行的一项辅助研究中,使用自我报告的客观数据评估了5至12岁轻度或中度哮喘儿童的依从性,并随机分配给200名儿童每天两次吸入微克布地奈德(n = 84)或安慰剂(n = 56),持续4年。 κ统计量用于评估自我报告的依从性(每日日记卡)和客观测量的依从性(研究吸入器中剩余的剂量数)之间的一致性。使用多变量分析来确定是否坚持研究治疗可以改变治疗相关的结局差异。结果:客观测量依从性时,在140名儿童中有75%的依从性低于80%,而通过自我报告进行测量时,只有6%的儿童依从性。客观和主观的依从性测量之间至少80%的一致性差(κ= 0.00; 95%CI,-0.05至0.04);四年内自我报告的依从性通常高估了客观衡量的依从性(93.6%对60.8%,P <.0001)。几乎没有证据表明依从性可以改变治疗相关的结局差异。结论:研究人员应使用客观而非依从性的依从性数据来鉴定对研究治疗依从性较低的临床试验参与者。

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