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布地奈德每日一次治疗早发型轻度持续性哮喘患者的长期安全性:早期哮喘吸入糖皮质激素常规治疗(START)研究结果

Long-term safety of once-daily budesonide in patients with early-onset mild persistent asthma: results of the Inhaled Steroid Treatment as Regular Therapy in Early Asthma (START) study.

作者信息

Sheffer Albert L, Silverman Mike, Woolcock Ann J, Díaz Patricia V, Lindberg Bengt, Lindmark Bertil

机构信息

Allergy Immunology Section, Brigham & Women's Hospital, Boston, Massachusetts 02467, USA.

出版信息

Ann Allergy Asthma Immunol. 2005 Jan;94(1):48-54. doi: 10.1016/S1081-1206(10)61285-9.

Abstract

BACKGROUND

The Inhaled Steroid Treatment as Regular Therapy in Early Asthma (START) study is a worldwide, randomized, prospective study to investigate early intervention with inhaled corticosteroids in recent-onset mild persistent asthma.

OBJECTIVE

To evaluate the safety and tolerability of long-term treatment with once-daily budesonide therapy in patients with mild persistent asthma.

METHODS

Patients aged 5 to 66 years with mild persistent asthma for fewer than 2 years and no previous regular corticosteroid treatment received budesonide or placebo once daily for 3 years, in addition to their usual asthma therapy. The daily budesonide dose was 200 microg for children younger than 11 years and 400 microg for those 11 years or older.

RESULTS

Overall, 7,221 patients were included in the safety analysis, and a total of 21,520 adverse events were reported (10,850 in the budesonide group and 10,670 in the placebo group). The most commonly reported events included respiratory infections, rhinitis, pharyngitis, bronchitis, viral infections, and sinusitis. The number of deaths and serious adverse events were similar for children and adults in both treatment groups. Fewer asthma-related serious adverse events were reported with budesonide (162) compared with placebo (276). Oral candidiasis was reported more frequently with budesonide (1.2%) than with placebo (0.5%); the frequencies of other adverse effects previously reported to be associated with inhaled corticosteroids (psychiatric disorders, skin disorders, and allergic reactions) were similar.

CONCLUSIONS

Three-year treatment with budesonide once daily (200 or 400 microg) is safe and well tolerated in children and adults with newly detected mild persistent asthma.

摘要

背景

吸入性糖皮质激素作为早期哮喘常规治疗(START)研究是一项全球性、随机、前瞻性研究,旨在调查吸入性糖皮质激素对近期起病的轻度持续性哮喘的早期干预效果。

目的

评估轻度持续性哮喘患者每日一次布地奈德长期治疗的安全性和耐受性。

方法

年龄在5至66岁、轻度持续性哮喘病程少于2年且既往未接受过常规糖皮质激素治疗的患者,除接受常规哮喘治疗外,每日接受一次布地奈德或安慰剂治疗,为期3年。11岁以下儿童每日布地奈德剂量为200微克,11岁及以上患者为400微克。

结果

总体而言,7221例患者纳入安全性分析,共报告21520例不良事件(布地奈德组10850例,安慰剂组10670例)。最常报告的事件包括呼吸道感染、鼻炎、咽炎、支气管炎、病毒感染和鼻窦炎。两个治疗组儿童和成人的死亡和严重不良事件数量相似。与安慰剂组(276例)相比,布地奈德组报告的哮喘相关严重不良事件较少(162例)。布地奈德组口腔念珠菌病报告频率(1.2%)高于安慰剂组(0.5%);先前报告的与吸入性糖皮质激素相关的其他不良反应(精神障碍、皮肤疾病和过敏反应)频率相似。

结论

对于新发现的轻度持续性哮喘儿童和成人,每日一次布地奈德(200或400微克)治疗3年是安全且耐受性良好的。

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