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吸入布地奈德在儿童中作为早期哮喘常规治疗的安全性和耐受性:类固醇治疗作为常规疗法(START)试验

Safety and tolerability of inhaled budesonide in children in the Steroid Treatment As Regular Therapy in early asthma (START) trial.

作者信息

Silverman Michael, Sheffer Albert L, Díaz Patricia V, Lindberg Bengt

机构信息

Department of Infection, Inflammation and Immunology, University of Leicester, Leicester, UK.

出版信息

Pediatr Allergy Immunol. 2006 May;17 Suppl 17:14-20. doi: 10.1111/j.1600-5562.2006.00380.x.

Abstract

The safety and tolerability of asthma medications are still a concern to many asthma patients receiving long-term treatment. Therefore, more safety data from long-term, controlled trials are needed. The aim of this study was to evaluate the safety and tolerability of long-term treatment with once-daily budesonide in children aged 5-10 yrs with mild persistent asthma of recent onset in the inhaled Steroid Treatment As Regular Therapy in early asthma (START) study. Children aged 5-10 yrs with early asthma were randomized to double-blind treatment with budesonide 200 microg or placebo once daily via Turbuhaler in addition to usual asthma therapy, for 3 yrs. Adverse events were recorded from both spontaneous reports and responses to standard questions, and asthma-related events and asthma control were recorded between visits and subsequently graded by the blinded investigators. Of the study population of 1981 children (1004 budesonide and 977 usual care), 81% (812 of 1004) in the budesonide group and 82% (797 of 977) in the usual care group experienced a total of 6414 events listed by preferred term (3209 budesonide plus usual care and 3205 placebo plus usual care). The most commonly reported events included respiratory infection, pharyngitis, rhinitis, viral infection and bronchitis, and there were no clinically relevant differences in incidence between treatments. There were no reports of tuberculosis or aspergillosis, and no evidence of increased risk of systemic or ocular adverse events with budesonide relative to placebo. There were 106 serious adverse events in the budesonide group and 128 with usual care. The most frequent, aggravated asthma, was more common with usual care than with budesonide. There were no deaths among children participating in START. In conclusion, the addition of once-daily inhaled budesonide 200 microg via Turbuhaler to usual care is safe and well tolerated in children with recent-onset mild persistent asthma.

摘要

哮喘药物的安全性和耐受性仍是许多接受长期治疗的哮喘患者所关心的问题。因此,需要来自长期对照试验的更多安全性数据。本吸入性糖皮质激素早期哮喘常规治疗(START)研究的目的是评估5至10岁近期起病的轻度持续性哮喘儿童长期每日一次使用布地奈德治疗的安全性和耐受性。5至10岁的早期哮喘儿童被随机分为双盲治疗组,除常规哮喘治疗外,通过都保装置每日一次吸入200微克布地奈德或安慰剂,为期3年。不良事件通过自发报告和对标准问题的回答进行记录,哮喘相关事件和哮喘控制情况在访视期间记录,并随后由盲法研究者进行分级。在1981名研究对象(1004名布地奈德组和977名常规治疗组)中,布地奈德组81%(1004名中的812名)和常规治疗组82%(977名中的797名)共经历了6414起按首选术语列出的事件(3209起布地奈德加常规治疗和3205起安慰剂加常规治疗)。最常报告的事件包括呼吸道感染、咽炎、鼻炎、病毒感染和支气管炎,各治疗组之间的发生率无临床相关差异。没有关于结核病或曲霉病的报告,也没有证据表明布地奈德相对于安慰剂会增加全身或眼部不良事件的风险。布地奈德组有106起严重不良事件,常规治疗组有128起。最常见的严重不良事件是哮喘加重,常规治疗组比布地奈德组更常见。参与START研究的儿童中没有死亡病例。总之,对于近期起病的轻度持续性哮喘儿童,在常规治疗基础上每日一次通过都保装置吸入200微克布地奈德是安全且耐受性良好的。

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