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Asthma Control in Young Children Treated with Once-Daily Budesonide Turbuhaler® Who Were Previously Treated with Budesonide Inhalation Suspension

机译:每天接受一次布地奈德吸入混悬液治疗的布地奈德Turbuhaler®每天治疗的儿童哮喘控制

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摘要

Budesonide inhalation suspension (Pulmicort Respules®), administered through jet nebulization, and budesonide dry powder inhaler (Pulmicort Turbuhaler®) are used for the treatment of asthma; however, the age indication for these products varies by country. In the United States, the indication for budesonide inhalation suspension is limited to children aged 12 months to 8 years. In many countries, budesonide Turbuhaler is indicated for use in children as young as 5 years. This clinical study assessed asthma control in children aged 4–6 years when transitioning from budesonide inhalation suspension to budesonide Turbuhaler. Ten children maintained on once-daily budesonide inhalation suspension (0.25 or 0.5 mg) were transitioned to once-daily budesonide Turbuhaler (200 μg) for 6 weeks after a 2-week run-in period, during which the original dose of budesonide inhalation suspension was continued. The primary outcome assessment was the change from baseline to the average during the last 2 weeks of treatment in morning and evening peak expiratory flow (PEF) measurements. Secondary outcomes were short-acting β2-adrenergic agonist (SABA) use, asthma symptom scores, and adverse events; peak inspiratory flow (PIF) also was assessed. Patients were able to maintain asthma control when transitioned from budesonide inhalation suspension to budesonide Turbuhaler. Mean improvements from baseline in morning and evening PEF were 19.1 and 16.8 L/min, respectively. At study end, no differences were observed in SABA use or daytime and nighttime asthma symptom scores compared with baseline. All but one patient demonstrated PIF values ≥30 L/min at all visits throughout the study. No unexpected adverse events were observed, and no patients discontinued from the study. These results suggest that children with asthma aged 4–6 years can successfully be transitioned from once-daily budesonide inhalation suspension to budesonide Turbuhaler while maintaining asthma control
机译:布地奈德吸入悬浮液(PulmicortRespules®)通过喷射雾化给药,布地奈德干粉吸入器(PulmicortTurbuhaler®)用于治疗哮喘;但是,这些产品的年龄指示因国家/地区而异。在美国,布地奈德吸入混悬剂的适应症仅限于12个月至8岁的儿童。在许多国家,布地奈德Turbuhaler被指定用于5岁以下的儿童。这项临床研究评估了从布地奈德吸入混悬液过渡到布地奈德Turbuhaler时4-6岁儿童的哮喘控制情况。在连续2周的磨合期后的6周内,将10名每天服用一次布地奈德吸入混悬液(0.25或0.5 mg)的儿童转入每天一次布地奈德Turbuhaler(200μg),持续6周。继续。主要结局评估是早晨和晚上峰值呼气流量(PEF)测量值在治疗的最后2周内从基线到平均值的变化。次要结果是使用短效β2-肾上腺素能激动剂(SABA),哮喘症状评分和不良事件。还评估了峰值吸气流量(PIF)。从布地奈德吸入混悬液过渡到布地奈德Turbuhaler时,患者能够维持哮喘控制。 PEF早上和晚上的基线平均改善分别为19.1和16.8 L / min。在研究结束时,与基线相比,在使用SABA或白天和夜间哮喘症状评分方面均未观察到差异。在整个研究过程中,除一名患者外,所有患者的PIF值均≥30 L / min。没有观察到意外的不良事件,也没有患者退出研究。这些结果表明,在维持哮喘控制的同时,可以成功地将4-6岁的哮喘儿童从每天一次的布地奈德吸入混悬液改为布地奈德Turbuhaler

著录项

  • 来源
    《Pediatric Asthma, Allergy & Immunology》 |2008年第3期|p.113-118|共6页
  • 作者

    Kevin R. Murphy.;

  • 作者单位

    Department of Allergy, Asthma, and Pediatric Pulmonology, Boys Town National Research Hospital, Omaha, Nebraska.;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Asthma;

    机译:哮喘;

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