Suppr超能文献

哮喘儿童长期吸入皮质类固醇(布地奈德)治疗的中断会导致病情恶化。荷兰中枢神经系统和肺部疾病研究小组。

Cessation of long-term treatment with inhaled corticosteroid (budesonide) in children with asthma results in deterioration. The Dutch CNSLD Study Group.

作者信息

Waalkens H J, Van Essen-Zandvliet E E, Hughes M D, Gerritsen J, Duiverman E J, Knol K, Kerrebijn K F

机构信息

Department of Pediatrics, University Hospital Groningen/Beatrix Children Clinic, The Netherlands.

出版信息

Am Rev Respir Dis. 1993 Nov;148(5):1252-7. doi: 10.1164/ajrccm/148.5.1252.

Abstract

Inhaled corticosteroid has been shown to be effective in the management of asthma. However, there is a lack of studies that assess the effect of cessation after long-term treatment with inhaled corticosteroid. This question was addressed in 28 children with stable asthma, aged 11 to 18 yr of age, who had completed 28 to 36 months of treatment with inhaled corticosteroid (budesonide 200 micrograms 3 times/day) and inhaled beta-2-agonist (salbutamol 200 micrograms 3 times/day). The children were randomized in a 1:2 ratio in a double-blind study either to continue budesonide (n = 8) during a period of 6 months or to decrease the dose of budesonide (n = 20) within 2 months, followed by placebo for 4 months. Treatment with salbutamol 600 micrograms daily was continued in both groups. Eight children from the tapering-off group withdrew, mainly due to symptoms of asthma, compared with none in the continuous treatment group. Five patients in the tapering-off group experienced exacerbations for which prednisolone was given, compared with none in the continuous treatment group. After tapering-off, symptoms of asthma and additional bronchodilator use increased, and both FEV1% predicted and PD20 histamine (provocation dose of histamine causing a 20% fall in FEV1) decreased, whereas these all remained unchanged in the group that continued treatment with inhaled corticosteroid. We conclude that in this study long-term treatment with 600 micrograms budesonide daily suppressed underlying mechanisms of asthma, but did not cure the disease.

摘要

吸入性糖皮质激素已被证明在哮喘管理中有效。然而,缺乏评估吸入性糖皮质激素长期治疗后停药效果的研究。本研究针对28名年龄在11至18岁、哮喘病情稳定的儿童,他们已完成28至36个月的吸入性糖皮质激素(布地奈德200微克,每日3次)和吸入性β-2激动剂(沙丁胺醇200微克,每日3次)治疗。在一项双盲研究中,这些儿童以1:2的比例随机分组,一组在6个月内继续使用布地奈德(n = 8),另一组在2个月内减少布地奈德剂量(n = 20),随后4个月使用安慰剂。两组均继续每日使用600微克沙丁胺醇治疗。减量组有8名儿童退出,主要原因是哮喘症状,而持续治疗组无儿童退出。减量组有5名患者哮喘加重并接受了泼尼松龙治疗,而持续治疗组无患者出现这种情况。减量后,哮喘症状和额外支气管扩张剂的使用增加,预计FEV1%和组胺PD20(引起FEV1下降20%的组胺激发剂量)降低,而继续吸入性糖皮质激素治疗组的这些指标均保持不变。我们得出结论,在本研究中,每日600微克布地奈德的长期治疗抑制了哮喘的潜在机制,但并未治愈该疾病。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验