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评估成人囊性纤维化气道清除技术的结局指标研究:一项单中心随机对照交叉试验方案。

Investigating outcome measures for assessing airway clearance techniques in adults with cystic fibrosis: protocol of a single-centre randomised controlled crossover trial.

机构信息

Adult Cystic Fibrosis, Royal Brompton Hospital, London, UK.

National Heart and Lung Institute, Imperial College London, London, UK.

出版信息

BMJ Open Respir Res. 2020 Oct;7(1). doi: 10.1136/bmjresp-2020-000694.

Abstract

INTRODUCTION

Airway clearance techniques (ACTs) are a gold standard of cystic fibrosis management; however, the majority of research evidence for their efficacy is of low standard; often attributed to the lack of sensitivity from outcome measures (OMs) used historically. This randomised controlled trial (RCT) investigates these standard OMs (sputum weight, forced expiratory volume in 1 s) and new OMs (electrical impedance tomography (EIT), multiple breath washout (MBW) and impulse oscillometry (IOS)) to determine the most useful measures of ACT.

METHODS AND ANALYSIS

This is a single-centre RCT with crossover design. Participants perform MBW, IOS and spirometry, and then are randomised to either rest or supervised ACT lasting 30-60 min. MBW, IOS and spirometry are repeated immediately afterwards. EIT and sputum are collected during rest/ACT. On a separate day, the OMs are performed with the other intervention. Primary endpoint is difference in change in OMs before and after ACT/rest. Sample size was calculated with 80% power and significance of 5% for each OM (target n=64).

ETHICS AND DISSEMINATION

Ethics approval was gained from the London-Chelsea Research Ethics Committee (reference 16/LO/0995, project ID 154635). Dissemination will involve scientific conference presentation and publication in a peer-reviewed journal.

TRIAL REGISTRATION NUMBERS

ISRCTN11220163 and NCT02721498.

摘要

简介

气道清除技术(ACT)是囊性纤维化管理的金标准;然而,其疗效的大多数研究证据标准较低;这主要归因于历史上使用的结局测量(OM)缺乏敏感性。这项随机对照试验(RCT)调查了这些标准 OM(痰量、1 秒用力呼气量)和新 OM(电阻抗断层扫描(EIT)、多次呼吸冲洗(MBW)和脉冲震荡(IOS)),以确定 ACT 最有用的测量指标。

方法与分析

这是一项单中心 RCT,采用交叉设计。参与者进行 MBW、IOS 和肺活量测定,然后随机分为休息或监督 ACT 持续 30-60 分钟。之后立即重复 MBW、IOS 和肺活量测定。休息/ACT 期间收集 EIT 和痰。在另一天,使用其他干预措施进行 OM。主要终点是 ACT/休息前后 OM 变化的差异。根据每个 OM(目标 n=64)的 80%功效和 5%显著性计算样本量。

伦理与传播

伦敦-切尔西研究伦理委员会已批准该研究(参考号 16/LO/0995,项目 ID 154635)。传播将包括科学会议报告和在同行评议期刊上发表。

试验注册号

ISRCTN8516034 和 NCT02721498。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fda0/7537140/144a81c262be/bmjresp-2020-000694f01.jpg

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