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首页> 外文期刊>Respiratory medicine >Ciclesonide in wheezy preschool children with a positive asthma predictive index or atopy.
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Ciclesonide in wheezy preschool children with a positive asthma predictive index or atopy.

机译:喘息型学龄前儿童哮喘发作预测指数或特应性呈阳性的Ciclesonide。

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BACKGROUND: Few large-scale studies have examined inhaled corticosteroid treatment in preschool children with recurrent wheeze. We assessed the effects of ciclesonide in preschool children with recurrent wheeze. METHODS: We included children 2-6 yrs with recurrent wheeze and a positive asthma predictive index or aeroallergen sensitization to, excluding patients with episodic viral wheezing. After a 2-4-week baseline period, patients with ongoing symptoms or rescue medication use were randomised to once-daily ciclesonide 40, 80, 160 mug or placebo for 24 weeks. RESULTS: The number of wheeze exacerbations requiring systemic corticosteroids was unexpectedly low in all groups: 25 (10.2%) in placebo group, as compared to 11 (4.4%), 18 (7.3%), and 17 (6.7%) in ciclesonide 40, 80, and 160 mug, respectively. The difference in time to first exacerbation was not significantly different between groups (p = 0.786), but the difference in exacerbation rates between placebo and the pooled ciclesonide groups was (p = 0.03). Large and significant (p < 0.0001) improvements in symptom scores and rescue medication use occurred in all groups, including placebo. Improvements in FEV(1) and FEF(25-75) (measured in 284 4-6 yr olds) were larger in the ciclesonide than in the placebo group. No differences in safety parameters (adverse events, height growth, serum and urinary cortisol levels) between ciclesonide and placebo were observed. CONCLUSIONS: In preschool children with recurrent wheeze and a positive asthma predictive index, ciclesonide modestly reduces wheeze exacerbation rates and improves lung function. A large placebo response and unexpected selection of patients with mild disease may have affected outcomes, highlighting the heterogeneity of preschool wheezing disorders.
机译:背景:很少有大规模的研究检查复发性喘息的学龄前儿童吸入糖皮质激素的治疗​​。我们评估了克索奈德在学龄前儿童反复喘息中的作用。方法:我们纳入了2至6岁的儿童,这些儿童患有反复发作的喘息且哮喘的预测指数或对空气过敏原的阳性反应为阳性,但不包括发作性病毒性喘息的患者。在2-4周的基线期后,将有持续症状或使用急救药物的患者随机分配至每日一次40、80、160马克杯或安慰剂的安慰剂组,持续24周。结果:所有系统中需要全身性皮质类固醇的喘息加重次数出乎意料地低:安慰剂组为25(10.2%),相比之下,倍可奈德40为11(4.4%),18(7.3%)和17(6.7%) ,80和160马克杯。两组之间第一次加重时间的差异无显着差异(p = 0.786),但安慰剂组和合并的库克索尼德组之间的加重率差异为(p = 0.03)。在所有症状组(包括安慰剂组)中,症状评分和急救药物的使用均显着改善(p <0.0001)。与安慰剂组相比,西索奈德的FEV(1)和FEF(25-75)改善(在284位4-6岁儿童中测得)更大。在西索奈德和安慰剂之间未观察到安全性参数(不良事件,身高增长,血清和尿皮质醇水平)的差异。结论:在哮喘反复发作且哮喘预测指数为阳性的学龄前儿童中,克索奈德可适度降低哮喘发作率并改善肺功能。较大的安慰剂反应和轻度疾病患者的意外选择可能会影响预后,从而突显了学龄前喘息障碍的异质性。

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