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一项累积剂量、安全性和耐受性研究阿福特罗在患有稳定型哮喘的儿科患者中的应用。

A cumulative dose, safety and tolerability study of arformoterol in pediatric subjects with stable asthma.

机构信息

Sunovion Pharmaceuticals Inc., 84 Waterford Drive, Marlborough, MA 01752, USA.

出版信息

Pediatr Pulmonol. 2011 Aug;46(8):761-9. doi: 10.1002/ppul.21446. Epub 2011 May 16.

Abstract

PURPOSE

Short-acting β(2) -agonists (SABAs) are recommended for treating acute pediatric asthma. The long-acting β(2) -agonist (LABA) arformoterol is approved for the maintenance treatment of chronic obstructive pulmonary disease (COPD). Arformoterol acts rapidly, is delivered via nebulization, and, as such, raises concerns from the FDA over possible off-label use in acute asthma in children. As a step to investigate this issue, this study evaluated the safety and tolerability of three consecutive doses of arformoterol administered over 1 hr in children with stable asthma.

METHODS

This study consisted of a double-blind, crossover period in which subjects (ages 2-11 years) with stable asthma were randomized to three consecutive nebulized doses of arformoterol (7.5 µg/dose) or levalbuterol (0.63 mg/dose) administered over 1-hr (0, 30, and 60 min) followed by an open-label period with three consecutive doses of arformoterol (15 µg/dose) administered over 1 hr. Endpoints were change in heart rate, blood pressure, and serum potassium and glucose levels. Other endpoints included adverse events and pulmonary function.

RESULTS

There were no clinically important mean changes from pre-dose in heart rate, blood pressure, or serum glucose levels, across treatment groups. Substantial declines in serum potassium levels were observed both 2 and 6 hr post-dosing. Two subjects had declines to 2.8 mEq/L and 2.9 mEq/L 2-hr post-dosing. Adverse events were infrequent and differences in forced expiratory volume in 1 sec and peak expiratory flow across treatment groups were not clinically meaningful.

CONCLUSION

In this study, in children with stable asthma, three consecutive doses of arformoterol (7.5 and 15 µg) and levalbuterol were overall well tolerated. Nonetheless, serum potassium levels demonstrated substantial mean declines after dosing. These findings do not address or support the safety and tolerability of arformoterol use in acute exacerbations of asthma in children.

摘要

目的

短效 β(2) -激动剂(SABA)被推荐用于治疗小儿急性哮喘。长效 β(2) -激动剂(LABA)沙美特罗(arformoterol)被批准用于慢性阻塞性肺病(COPD)的维持治疗。沙美特罗起效迅速,通过雾化吸入给药,这引起了 FDA 对其在儿童急性哮喘中可能被超说明书使用的担忧。作为调查这一问题的一步,本研究评估了三剂连续沙美特罗在稳定哮喘儿童中 1 小时内给药的安全性和耐受性。

方法

这是一项双盲、交叉研究,其中患有稳定哮喘的受试者(年龄 2-11 岁)被随机分配接受三剂连续雾化沙美特罗(7.5 µg/剂)或特布他林(0.63 mg/剂),1 小时内(0、30 和 60 分钟)给药,随后进行开放标签期,三剂连续沙美特罗(15 µg/剂)在 1 小时内给药。终点是心率、血压和血清钾、血糖水平的变化。其他终点包括不良事件和肺功能。

结果

在治疗组中,心率、血压或血清葡萄糖水平从基线没有出现有临床意义的平均变化。给药后 2 小时和 6 小时观察到血清钾水平显著下降。2 小时后有 2 名受试者的血清钾水平下降至 2.8 mEq/L 和 2.9 mEq/L。不良事件很少见,各组间用力呼气量 1 秒和呼气峰流速的差异无临床意义。

结论

在这项研究中,患有稳定哮喘的儿童连续三剂沙美特罗(7.5 和 15 µg)和特布他林总体耐受性良好。然而,给药后血清钾水平明显下降。这些发现并未解决或支持沙美特罗在儿童哮喘急性发作中使用的安全性和耐受性。

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