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Asthma drug adherence in a long term clinical trial.

机译:长期临床试验中对哮喘药物的依从性。

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AIM: To measure drug adherence in children with mild asthma receiving long term prophylactic treatment. METHODS: Double blind randomised placebo controlled trial. Patients received inhaled budesonide 100 microg or 200 microg daily, or placebo for 27 months. All participants were asked to inhale medication or placebo from two different Turbuhalers (morning and evening) during the study. A total of 122 children (80 boys, 42 girls) aged 7-16 years with mild asthma (mean FEV(1) 103.7% of predicted) were included in the trial. Drug adherence was assessed by counting the number of remaining doses in the inhaler when study medication was returned at six month intervals. RESULTS: A statistically significant and continuing decrease in measured drug adherence was found from three to nine months and then to 27 months, reaching mean values of 40.6% and 46. 9% for inhaled morning and evening medication respectively. Drug adherence declined more rapidly in the placebo group (compared to active treatment); this difference became significant after two years of treatment. Children aged 9 years or less had better drug adherence during the entire study period, but the difference was only significant for the first three months of the study. Measured drug adherence was significantly higher for evening medication compared to morning medication for all study intervals after nine months. CONCLUSION: Measured drug adherence diminishes significantly when treating children with mild asthma in a long term trial. This emphasises the importance of monitoring compliance in clinical trials.
机译:目的:测量接受长期预防治疗的轻度哮喘患儿的药物依从性。方法:双盲随机安慰剂对照试验。患者每天吸入100微克或200微克布地奈德,或接受安慰剂治疗27个月。在研究过程中,要求所有参与者从两个不同的Turbuhalers吸入药物或安慰剂(早上和晚上)。该试验共纳入122例7-16岁,患有轻度哮喘(平均FEV(1)为预测值的103.7%)的儿童(80名男孩,42名女孩)。通过计算每六个月退回研究药物时吸入器中的剩余剂量数来评估药物依从性。结果:从3到9个月,然后到27个月,测量到的药物依从性在统计学上持续显着下降,早晨和晚上吸入药物的平均值分别达到40.6%和46. 9%。安慰剂组的药物依从性下降更快(与积极治疗相比);经过两年的治疗,这种差异变得很明显。 9岁或以下的儿童在整个研究期间的药物依从性更好,但差异仅在研究的前三个月才显着。在九个月后的所有研究间隔中,夜间药物的测量药物依从性均明显高于早晨药物。结论:在长期试验中,治疗轻度哮喘患儿时,测得的药物依从性显着降低。这强调了在临床试验中监测依从性的重要性。

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