肺活量测定法治疗儿童哮喘:一项随机对照试验研究方案(SPIROMAC)。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-09-29 DOI:10.1186/s13063-025-09104-1
Victoria Bell, Nicole Sergenson, Seonaidh Cotton, Chukwuemeka David Emele, Ruth Thomas, Lorna Aucott, Mark Forrest, Erol A Gaillard, Erika J Kennington, Graeme MacLennan, Ian Sinha, Thenmalar Vadiveloo, Neil W Scott, Steve Turner
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引用次数: 0

摘要

背景:哮喘影响着英国100多万儿童,预防性治疗是由患者症状主观上指导的。肺活量测定法是一种客观的肺功能测试,可用于儿童指导治疗。然而,目前的指南并没有指出在肺活量测定结果改变的情况下哮喘治疗应该如何改变。本研究将评估肺活量测定法如何用于指导哮喘治疗和降低儿童哮喘发作的风险。方法:这是一项多中心、随机对照试验。6-15岁的儿童,如果诊断为哮喘,并且在过去12个月内病情加重,需要口服或静脉注射皮质类固醇,将符合条件。排除标准包括基线评估时无法提供肺活量测定,患有其他慢性呼吸疾病,目前正在接受维持性口服类固醇或生物制剂治疗。参与者将在初级和二级保健机构中招募,并将随机分组,接受由肺活量测量加症状指导的哮喘治疗(干预组)或仅由症状指导的哮喘治疗(标准护理组)。在肺活量测定组,治疗建议将取决于肺活量测定的变化。参与者将在随机化后3、6、9和12个月参加评估,并提出治疗建议。主要结局是参与者或父母记录的每名参与者在12个月内需要1-7天口服或静脉注射皮质类固醇治疗的哮喘发作次数。次要结局包括首次发作时间、任何哮喘发作、不良事件、吸入皮质类固醇剂量、哮喘控制和生活质量。通过电子记录设备测量吸入皮质类固醇治疗的依从性。讨论:本研究将评估肺活量测定法指导下的哮喘治疗是否会减少儿童未来的哮喘发作。我们的发现可能与国家和国际哮喘指南有关。试验注册号:ISRCTN, ISRCTN31849868。2022年7月1日注册前瞻性登记。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spirometry to manage asthma in children: study protocol for a randomised controlled trial (SPIROMAC).

Background: Asthma affects over 1 million children across the UK, and preventative treatment is guided subjectively by patient symptoms. Spirometry is an objective test of lung function and can be used in children to guide treatment. However, current guidelines do not indicate how asthma treatment should change in the context of changing spirometry results. This study will evaluate how spirometry can be used to guide asthma treatment and reduce the risk for asthma attacks in children.

Methods: This is a multi-centre, randomised controlled trial. Children aged 6-15 years, who have a diagnosis of asthma and have had an exacerbation requiring oral or intravenous corticosteroids in the previous 12 months, will be eligible. Exclusion criteria include being unable to provide spirometry measurement at baseline assessment, having another chronic respiratory condition and being currently treated with maintenance oral steroids or biologicals. Participants will be recruited in both primary and secondary care settings and will be randomised to either receive asthma treatment guided by spirometry plus symptoms (intervention group) or asthma treatment guided by symptoms only (standard care group). Within the spirometry group, treatment recommendations will be dependent on changes in spirometry measurements. Participants will attend assessments 3, 6, 9 and 12 months post-randomisation, where treatment recommendations will be made. The primary outcome is the number of asthma attacks per participant requiring treatment with 1-7 days of oral or intravenous corticosteroid over 12 months, as recorded by the participant or parent. Secondary outcomes include time to first attack, any asthma attack, adverse events, dose of inhaled corticosteroids, asthma control and quality of life. Adherence to inhaled corticosteroid treatment is measured by an electronic logging device.

Discussion: This study will evaluate whether asthma treatment guided by spirometry will reduce future asthma attacks in children. Our findings may be relevant to national and international asthma guidelines.

Trial registration: ISRCTN, ISRCTN31849868. Registered on 01.07.2022. Prospectively registered.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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