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关于干粉吸入器在儿童哮喘维持治疗和急性加重期治疗中临床有效性的系统评价。

A systematic review of the clinical effectiveness of dry powder inhalers in maintenance treatment and in treatment of acute exacerbations of asthma in children.

作者信息

Twohig Helen, Franklin Lauren, Carroll Will, Corp Nadia, Jackson Emma, Mallen Christian, Ruan Bernice, Yapp Louisa, Der Windt Danielle Van, Smith James

机构信息

School of Medicine, Keele University, Keele, Staffordshire ST5 5BG, the United Kingdom of Great Britain and Northern Ireland.

School of Medicine, Keele University, Keele, Staffordshire ST5 5BG, the United Kingdom of Great Britain and Northern Ireland.

出版信息

Paediatr Respir Rev. 2025 Apr 16. doi: 10.1016/j.prrv.2025.04.005.

Abstract

BACKGROUND

Dry powder inhalers (DPIs) are a lower-carbon option than pressurised metered dose inhalers (pMDIs). However, DPIs require a forceful inhalation to achieve good lung deposition and there is uncertainty as to whether younger children can effectively use DPIs for maintenance treatment or rely upon them during exacerbations.

METHODS

We searched electronic databases to identify randomised trials of children with asthma receiving treatment delivered via DPI, either for maintenance treatment (children ≤ 12 years) or for an acute exacerbation (participants up to age 18). Screening and data extraction were carried out by two reviewers. Risk of bias (RoB) assessment was made using the Cochrane RoB2 tool. Findings were narratively synthesised and a modified GRADE approach was taken to summarise the strength of evidence.

RESULTS

27 studies were included. 20 addressed maintenance treatment in children ≤ 12 years although only 4 compared the same treatment delivered via pMDI to DPI. All found no difference in efficacy between the device types (high certainty evidence). Other studies provided weaker, indirect evidence supporting this finding. 7 studies considered acute asthma in hospital/emergency settings. All reported no difference in efficacy between device types but certainty of evidence was low due to high RoB and clinical and methodological heterogeneity.

CONCLUSION

There are few studies directly comparing treatment via DPI/pMDI for asthma in children. Comparative studies suggest that for children who can use both DPI/pMDI, the devices are equal in efficacy for maintenance treatment in children ≤ 12 years but high-quality evidence is lacking regarding their use during acute exacerbations. This review did not find sufficient evidence to identify a lower age at which DPIs can start being used.

摘要

背景

与压力定量吸入器(pMDIs)相比,干粉吸入器(DPIs)是一种低碳选择。然而,DPIs 需要用力吸气才能实现良好的肺部沉积,对于年幼儿童能否有效地使用 DPIs 进行维持治疗或在病情加重时依赖它们存在不确定性。

方法

我们检索了电子数据库,以确定接受通过 DPI 给药治疗的哮喘儿童的随机试验,这些试验要么用于维持治疗(≤12 岁儿童),要么用于急性加重期治疗(年龄最大 18 岁的参与者)。由两名评审员进行筛选和数据提取。使用 Cochrane RoB2 工具进行偏倚风险(RoB)评估。对研究结果进行叙述性综合,并采用改良的 GRADE 方法总结证据强度。

结果

纳入了 27 项研究。20 项研究针对≤12 岁儿童的维持治疗,尽管只有 4 项研究比较了通过 pMDI 和 DPI 给予相同治疗的效果。所有研究均发现不同装置类型之间在疗效上无差异(高确定性证据)。其他研究提供了较弱的间接证据支持这一发现。7 项研究考虑了医院/急诊环境中的急性哮喘。所有研究均报告不同装置类型之间在疗效上无差异,但由于高 RoB 以及临床和方法学异质性,证据的确定性较低。

结论

直接比较 DPI/pMDI 治疗儿童哮喘的研究很少。比较研究表明,对于能够同时使用 DPI/pMDI 的儿童,这些装置在≤12 岁儿童的维持治疗中疗效相当,但在急性加重期使用时缺乏高质量证据。本综述未找到足够证据来确定可以开始使用 DPI 的更低年龄。

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