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丙酸氟替卡松/沙美特罗与丙酸氟替卡松单药治疗在儿童哮喘升级治疗中的疗效和安全性:系统评价和荟萃分析。

Efficacy and safety of fluticasone propionate/salmeterol and fluticasone propionate monotherapy in step-up treatment of childhood asthma: A systematic review and meta-analysis.

机构信息

Department of Pharmacy, Shanxi Provincial Children's Hospital, Taiyuan, Shanxi, China.

Department of Pharmacy, Beijing Hospital of Integrated Traditional Chinese and Western Medicine, Beijing, China.

出版信息

Heart Lung. 2024 Jan-Feb;63:23-34. doi: 10.1016/j.hrtlng.2023.09.004. Epub 2023 Sep 21.

Abstract

BACKGROUND

Asthma is a chronic respiratory disease that affects millions of children worldwide and can impair their quality of life and development. Inhaled glucocorticoids are the mainstay of asthma treatment, but some children require step-up therapy with additional drugs to achieve symptom control. Fluticasone propionate and salmeterol (FSC) has been shown to reduce asthma exacerbations and improve lung function in adults. However, the evidence for its efficacy and safety in children is limited.

OBJECTIVE

This study aims to provide a comprehensive basis for treatment selection by summarizing existing clinical randomized controlled trials (RCTs) on the efficacy of FSC compared to fluticasone propionate (FP) monotherapy in children with asthma who require step-up treatment.

METHODS

Five online databases and three clinical trial registration platforms were systematically searched. The effect size and corresponding 95% confidence interval (CI) were calculated based on the heterogeneity among the included studies.

RESULTS

Twelve RCTs were identified and a total of 9, 859 patients were involved. The results of the meta-analysis revealed that the use of FSC was associated with a greater reduction in the incidence of asthma exacerbations than FP alone when the dose of FP was the same or when the duration of treatment exceeded 12 weeks. In addition, FSC resulted in a greater proportion of time with asthma-free and without the use of albuterol compared to FP alone when the duration of treatment exceeded 12 weeks. No significant differences were observed between FSC and FP alone in the incidence of drug-related adverse events and other adverse events.

CONCLUSION

Both FSC and FP alone are viable options for the initial selection of step-up treatment in asthmatic children. While, FSC treatment demonstrates a greater likelihood of reducing asthma exacerbations which is particularly important for reducing the personnel, social and economic burden in children requiring step-up asthma treatment.

摘要

背景

哮喘是一种影响全球数百万儿童的慢性呼吸道疾病,可降低他们的生活质量和发育水平。吸入性糖皮质激素是哮喘治疗的主要手段,但有些儿童需要使用附加药物进行升级治疗以实现症状控制。丙酸氟替卡松/沙美特罗(FSC)已被证明可减少成人哮喘恶化并改善肺功能。然而,其在儿童中的疗效和安全性证据有限。

目的

本研究旨在通过总结现有的关于丙酸氟替卡松(FP)单药治疗与 FSC 治疗哮喘升级治疗患儿的疗效的临床随机对照试验(RCT),为治疗选择提供综合依据。

方法

系统检索了 5 个在线数据库和 3 个临床试验注册平台。根据纳入研究的异质性,计算了效应量及其相应的 95%置信区间(CI)。

结果

共确定了 12 项 RCT,共涉及 9859 名患者。荟萃分析结果显示,当 FP 剂量相同时或治疗持续时间超过 12 周时,与 FP 单药相比,使用 FSC 可更大程度地降低哮喘恶化的发生率。此外,当治疗持续时间超过 12 周时,与 FP 单药相比,FSC 可使更多的时间无哮喘发作且无需使用沙丁胺醇。在药物相关不良事件和其他不良事件的发生率方面,FSC 与 FP 单药之间无显著差异。

结论

FSC 和 FP 单药均可作为哮喘儿童升级治疗的初始选择。虽然 FSC 治疗更有可能降低哮喘恶化的发生率,这对于减少需要升级治疗的哮喘患儿的人员、社会和经济负担尤为重要。

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