Jónasson G, Carlsen K H, Jonasson C, Mowinckel P
Paediatric Section for Allergy and Pulmonology, Ullevål Hospital, Oslo, Norway.
Allergy. 2000 Aug;55(8):740-8. doi: 10.1034/j.1398-9995.2000.00661.x.
This study is an extended follow-up for 24 months of a 12-week trial to study the long-term clinical efficacy of low-dose inhaled budesonide (BUD) once or twice daily in children with mild asthma. A total of 122 children (mean age 9.7 years, girls/boys; 42/80) with mild asthma (FEV1 103.7% of predicted, reversibility in FEV1 3.5%, and fall in FEV1 after exercise 12.2%), not previously treated with inhaled steroids, were included in a double-blind, randomized, parallel-group study. The children were treated with inhaled BUD 100 or 200 microg administered via Turbuhaler once daily in the morning, 100 microg twice daily, or placebo for 27 months. Exercise and methacholine challenges were performed at 3-month intervals the first year and at 6-month intervals the second year, in a total of seven visits. A significant dose-response effect favoring BUD 200 microg daily (vs 100 microg daily) was found when comparing changes in FEV1, FEF25%, and FEV50%; the fall in FEV1 after an exercise test; and the effect on blood eosinophils. Bronchial hyperreactivity to methacholine decreased significantly on three visits in patients treated with BUD 200 microg daily compared to placebo. Growth rate was not significantly affected except in children aged 7-11 years at baseline after 12 months of treatment. In conclusion, 100 or 200 microg daily of inhaled BUD for 27 months is safe and effective in protecting against exercise-induced asthma and achieving nearly normal lung function. Baseline lung function was not significantly affected in this group of children with mild asthma.
本研究是一项为期12周试验的24个月延长随访,旨在研究低剂量吸入布地奈德(BUD)每日一次或两次用于轻度哮喘儿童的长期临床疗效。共有122名轻度哮喘儿童(平均年龄9.7岁,女孩/男孩:42/80)纳入一项双盲、随机、平行组研究,这些儿童此前未接受过吸入性类固醇治疗(第一秒用力呼气容积[FEV1]为预测值的103.7%,FEV1可逆性为3.5%,运动后FEV1下降12.2%)。儿童接受吸入性BUD 100或200微克,通过都保装置于每天早晨给药一次,或100微克每日给药两次,或给予安慰剂,为期27个月。第一年每3个月、第二年每6个月进行一次运动和乙酰甲胆碱激发试验,共随访7次。比较FEV1、25%用力呼气流量(FEF25%)和50%用力呼气流量(FEV50%)的变化、运动试验后FEV1的下降以及对血液嗜酸性粒细胞的影响时,发现存在显著的剂量反应效应,支持每日200微克BUD(对比每日100微克BUD);与安慰剂相比,接受每日200微克BUD治疗的患者在三次随访中对乙酰甲胆碱的支气管高反应性显著降低。除了基线年龄为7至11岁的儿童在治疗12个月后,生长速率未受到显著影响。总之,每日吸入100或200微克BUD,持续27个月,对于预防运动诱发的哮喘和实现接近正常的肺功能是安全有效的。在这组轻度哮喘儿童中,基线肺功能未受到显著影响。