Suppr超能文献

在中国,用低剂量布地奈德混悬液吸入疗法治疗小儿轻度持续性哮喘与孟鲁司特钠的对比。

Treatment of pediatric mild persistent asthma with low-dose budesonide inhalation suspension vs. montelukast in China.

机构信息

Department of Respiratory Diseases, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310006, China.

Department of Respiratory Diseases, Children's Hospital of Nanjing Medical University, Nanjing, 210029, China.

出版信息

World J Pediatr. 2021 Dec;17(6):619-625. doi: 10.1007/s12519-021-00464-7. Epub 2021 Oct 6.

Abstract

BACKGROUND

There are limited studies comparing budesonide inhalation suspension (BIS) with montelukast in real-world settings where treatment adherence and persistency may be suboptimal. This real-world study aims to investigate the control effectiveness of montelukast or BIS as a monotherapy in Chinese children with mild asthma.

METHODS

Data were derived from a retrospective questionnaire-based analysis of 2‒14-year-old children with mild persistent asthma, who received either 500 µg of BIS (n = 153) or 4‒5 mg of montelukast (n = 240) once daily. The indicators of asthma control, the Asthma Control Test (ACT)/Childhood ACT (C-ACT) score, and the asthma-related medical costs were assessed. The differences between the two groups were compared using an unpaired t-test (normally distributed), Mann-Whitney U test (non-normally distributed) or chi-squared test (categorical variables).

RESULTS

Medication compliance in the past 3-month period was better in the montelukast group than in the BIS group (P = 0.042). The montelukast group exhibited better asthma control in the past 4-week period, including lower percentages of asthmatic children with symptoms more than twice a week (P = 0.021), had night waking or night coughing (P = 0.022), or required reliever medication more than twice a week (P < 0.001). The montelukast group had a lower percentage of children with an ACT/C-ACT score ≤ 19 (P = 0.015). Caregivers reported a significantly better exercise tolerance in the children who received montelukast vs. BIS in the past 12 months (P < 0.001). Significantly higher medical expenditures attributable to asthma in the past 12 months were observed in the BIS group vs. montelukast group (P < 0.001).

CONCLUSION

Both treatments provided acceptable overall asthma control in children with mild persistent asthma; however, more reliever medication and more medical expenditures attributable to asthma were needed for BIS vs. montelukast in real-world settings, where factors such as compliance were also taken into account.

摘要

背景

在治疗依从性和持久性可能不理想的真实环境中,比较布地奈德吸入悬浮液(BIS)和孟鲁司特的研究有限。本真实世界研究旨在调查孟鲁司特或 BIS 作为单一疗法在患有轻度哮喘的中国儿童中的控制效果。

方法

数据来自对接受 500μg BIS(n=153)或 4-5mg 孟鲁司特(n=240)的 2-14 岁轻度持续性哮喘儿童进行回顾性问卷调查分析。评估哮喘控制指标、哮喘控制测试(ACT)/儿童 ACT(C-ACT)评分和哮喘相关医疗费用。使用配对 t 检验(正态分布)、Mann-Whitney U 检验(非正态分布)或卡方检验(分类变量)比较两组之间的差异。

结果

在过去 3 个月期间,孟鲁司特组的药物依从性优于 BIS 组(P=0.042)。在过去 4 周期间,孟鲁司特组的哮喘控制更好,包括每周出现症状超过两次的哮喘儿童比例较低(P=0.021)、夜间醒来或夜间咳嗽(P=0.022)或每周需要缓解药物超过两次(P<0.001)。孟鲁司特组 ACT/C-ACT 评分≤19 的儿童比例较低(P=0.015)。在过去 12 个月期间,接受孟鲁司特的儿童的运动耐量明显优于接受 BIS 的儿童(P<0.001)。在过去 12 个月期间,BIS 组归因于哮喘的医疗支出明显高于孟鲁司特组(P<0.001)。

结论

在患有轻度持续性哮喘的儿童中,两种治疗方法均提供了可接受的总体哮喘控制;然而,在考虑到依从性等因素的真实环境中,BIS 比孟鲁司特需要更多的缓解药物和更多归因于哮喘的医疗支出。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验