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吸入性皮质类固醇(布地奈德)长期治疗后儿童哮喘的缓解:能否实现?荷兰中枢神经系统和肺部疾病研究组

Remission of childhood asthma after long-term treatment with an inhaled corticosteroid (budesonide): can it be achieved? Dutch CNSLD Study Group.

作者信息

van Essen-Zandvliet E E, Hughes M D, Waalkens H J, Duiverman E J, Kerrebijn K F

机构信息

Dept of Paediatrics, Erasmus University of Rotterdam, The Netherlands.

出版信息

Eur Respir J. 1994 Jan;7(1):63-8. doi: 10.1183/09031936.94.07010063.

Abstract

This study was undertaken in order to determine whether long-term treatment with inhaled corticosteroid can induce a remission in childhood asthma, and to decide when stabilization of airway responsiveness occurred. We therefore carried out, an extended follow-up of 28-36 months in one of two groups of children who participated in a long-term intervention study. This former study had shown that long-term (median follow-up 22 months) treatment with inhaled corticosteroid plus beta 2-agonist improves symptoms, airway calibre and airway responsiveness in children with asthma, compared with beta 2-agonist alone. On treatment with inhaled corticosteroid plus beta 2-agonist, airway calibre did not further improve after 4 months, whereas the provocative dose of histamine which causes a 20% fall in forced expiratory volume in one second (PD20) histamine showed gradual improvement without reaching an apparent plateau. Remission was defined as being symptom free during any 8 month period. Of the 58 children originally randomized to receive 0.2 mg salbutamol, plus 0.2 mg budesonide, t.i.d., five children withdrew: three due to lack of motivation, one for psychological reasons, and one due to a deterioration of asthma. One patient was hospitalized because of an asthma exacerbation. Airway calibre showed no improvement after 4 months up to 36 months. Mean PD20 histamine stabilized after 20 months at 2.1 doubling doses above baseline, but at a subnormal level of 80 micrograms. Symptoms improved during the first 18 months, and may have been improving further, but slowly, during the period between 18 and 36 months.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在确定吸入性糖皮质激素的长期治疗是否能使儿童哮喘缓解,并确定气道反应性何时稳定。因此,我们对参与一项长期干预研究的两组儿童中的一组进行了28至36个月的延长随访。之前的这项研究表明,与单独使用β2激动剂相比,吸入性糖皮质激素加β2激动剂的长期治疗(中位随访22个月)可改善哮喘儿童的症状、气道口径和气道反应性。在使用吸入性糖皮质激素加β2激动剂治疗时,4个月后气道口径未进一步改善,而导致一秒用力呼气量下降20%的组胺激发剂量(PD20组胺)则显示出逐渐改善,且未达到明显的平台期。缓解定义为在任何8个月期间无症状。最初随机接受每日三次0.2毫克沙丁胺醇加0.2毫克布地奈德治疗的58名儿童中,有5名儿童退出:3名因缺乏积极性,1名因心理原因,1名因哮喘恶化。1名患者因哮喘加重住院。4个月至36个月期间气道口径无改善。平均PD20组胺在20个月后稳定在高于基线2.1倍剂量水平,但处于80微克的低于正常水平。症状在最初18个月有所改善,在18至36个月期间可能仍在进一步改善,但改善缓慢。(摘要截断于250字)

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