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福莫特罗在儿童和青少年中的安全性:来自哮喘临床试验的经验。

Safety of formoterol in children and adolescents: experience from asthma clinical trials.

机构信息

King's College Hospital, London, UK.

出版信息

Arch Dis Child. 2010 Dec;95(12):1047-53. doi: 10.1136/adc.2010.183814. Epub 2010 Oct 27.

Abstract

BACKGROUND

The safety of long-acting β(2) agonist (LABA) therapy in asthma remains controversial but no large scale analyses have been published of LABA safety in children.

METHODS

The frequency of asthma-related deaths and hospitalisations following formoterol use in children (4-11 years) and adolescents (12-17 years), compared with non-LABA treatment, was assessed in all AstraZeneca-sponsored, randomised, controlled, parallel-group trials (≥3 months) where formoterol was used as maintenance and/or as reliever therapy.

RESULTS

11,849 children and adolescents under the age of 18 years from 41 trials were identified, 82% of whom used an inhaled corticosteroid (ICS) as concomitant medication. The number of asthma-related deaths (one 13-year-old boy among 7796 formoterol-treated patients, and none among 4053 non-LABA-treated patients) was too low to allow any between-group comparison. The frequency of patients with asthma-related hospitalisations was not different in formoterol-treated versus non-LABA-treated patients, either in children (1.16% (38/3263) vs 1.11% (24/2165)) or in adolescents (0.51% (23/4533) vs 0.85% (16/1888)). Asthma-related hospitalisations based on daily dose of formoterol were: (A) 4.5 or 9 µg: 1.9% (18/980); (B) 18 µg: 0.5% (14/2870); (C) 36 µg: 0% (0/67); and (D) variable dosing: 0.75% (29/3879). There was no difference between formoterol-treated and non-LABA-treated patients as regards ethnicity.

CONCLUSIONS

Formoterol use in children and adolescents (4-17 years) with asthma in this large study where the majority are prescribed concomitant ICS is not associated with any increased risk of asthma-related hospitalisations. The results are not influenced by dose or ethnicity.

摘要

背景

长效β2 激动剂(LABA)在哮喘治疗中的安全性仍存在争议,但尚未发表关于儿童使用 LABA 的安全性的大规模分析。

方法

在所有阿斯利康赞助的、随机、对照、平行组试验(≥3 个月)中,评估了在儿童(4-11 岁)和青少年(12-17 岁)中使用福莫特罗与非 LABA 治疗相比,与哮喘相关的死亡和住院的频率,福莫特罗被用作维持和/或缓解治疗。

结果

在 41 项试验中确定了 11849 名年龄在 18 岁以下的儿童和青少年,其中 82%的人同时使用吸入皮质类固醇(ICS)。与哮喘相关的死亡人数(1 名 13 岁男孩在 7796 名福莫特罗治疗患者中,而在 4053 名非 LABA 治疗患者中没有)太少,无法进行任何组间比较。在儿童(1.16%(38/3263)与非 LABA 治疗患者中 1.11%(24/2165))或青少年(0.51%(23/4533)与非 LABA 治疗患者中 0.85%(16/1888))中,福莫特罗治疗与非 LABA 治疗患者的哮喘相关住院率无差异。基于福莫特罗的日剂量,哮喘相关住院率为:(A)4.5 或 9μg:1.9%(18/980);(B)18μg:0.5%(14/2870);(C)36μg:0%(0/67);(D)剂量变化:0.75%(29/3879)。福莫特罗治疗组和非 LABA 治疗组的种族之间没有差异。

结论

在这项大型研究中,大多数患者同时处方 ICS,在患有哮喘的儿童和青少年(4-17 岁)中使用福莫特罗与任何与哮喘相关的住院风险增加无关。结果不受剂量或种族的影响。

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