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多中心双盲随机对照试验:对于因高嗜酸性粒细胞水平而住院的慢性阻塞性肺疾病急性加重患者,系统性皮质类固醇治疗:ECHO 方案。

Multicentre double-blind randomised controlled trial of systematic corticosteroid therapy in patients with acute exacerbations of chronic obstructive pulmonary disease admitted to hospital with higher eosinophil levels: the ECHO protocol.

机构信息

Department of Clinical Epidemiology, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

Department of Respiratory and Critical Care Medicine, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

出版信息

BMJ Open. 2023 May 29;13(5):e066354. doi: 10.1136/bmjopen-2022-066354.

Abstract

INTRODUCTION

Corticosteroid is one of the most commonly used medications in patients with acute exacerbations of chronic obstructive pulmonary disease (AECOPD). The increasing understanding of these side-effects of systematic corticosteroids and their better response to treatment among patients with COPD with higher blood eosinophil counts has led to an interest in a more targeted approach to systematic corticosteroid treatment. However, there is a lack of evidence from high-quality randomised controlled trial (RCT) studies about whether initial systematic corticosteroids should be given to patients with AECOPD with elevated eosinophilia. The aim of the present research was to test this hypothesis.

METHODS AND ANALYSIS

This is a multicentre, double-blind, superiority RCT in the respiratory departments of 12 general hospitals in China. It is anticipated that 456 patients with AECOPD with a blood eosinophil count >2% or >300 cells/µL at admission will be recruited. Eligible patients will be randomised (1:1) to the intervention group receiving 40 mg oral prednisone daily or identical-appearing placebo (control group) for five consecutive days. Follow-up visits are performed during hospitalisation, followed by clinic interviews on days 30, 60 and 90 after discharge. The primary outcome is treatment failure rates comprising requiring or receiving invasive or non-invasive mechanical ventilation, requiring or transferring to intensive care unit during the index hospitalisation, length of index hospitalisation longer than 14 days, death during the index hospitalisation or within 30 days after discharge and readmission with acute exacerbations of COPD within 30 days after discharge. The results of this trial will provide insight into the value of using blood eosinophil counts as a biomarker of eosinophilic exacerbation and initiating systematic corticosteroid treatment for patients with AECOPD with higher eosinophil levels.

ETHICS AND DISSEMINATION

This study was approved by Beijing Chaoyang Hospital Institutional Review Board (approval number: 2020-KE-544) and the main results and secondary results will be published in peer-reviewed journals.

TRIAL REGISTRATION NUMBER

NCT05059873.

摘要

简介

皮质类固醇是治疗慢性阻塞性肺疾病急性加重(AECOPD)患者的常用药物之一。越来越多的人认识到系统性皮质类固醇的这些副作用,以及更高血嗜酸性粒细胞计数的 COPD 患者对治疗的更好反应,这使得人们对系统性皮质类固醇治疗的更具针对性的方法产生了兴趣。然而,目前缺乏高质量随机对照试验(RCT)研究的证据,无法确定是否应给予嗜酸性粒细胞升高的 AECOPD 患者初始系统性皮质类固醇治疗。本研究旨在验证这一假说。

方法与分析

这是一项在中国 12 家综合医院呼吸科进行的多中心、双盲、优效性 RCT。预计将招募 456 名入院时血嗜酸性粒细胞计数>2%或>300 细胞/μL 的 AECOPD 患者。符合条件的患者将被随机(1:1)分为干预组,每天接受 40mg 口服泼尼松或相同外观的安慰剂(对照组),连续 5 天。在住院期间进行随访,然后在出院后第 30、60 和 90 天进行门诊访谈。主要结局是治疗失败率,包括需要或接受有创或无创机械通气、在指数住院期间需要或转至重症监护病房、指数住院时间超过 14 天、住院期间或出院后 30 天内死亡以及出院后 30 天内因 COPD 急性加重再次入院。这项试验的结果将为使用血嗜酸性粒细胞计数作为嗜酸性粒细胞加重的生物标志物,并为血嗜酸性粒细胞计数较高的 AECOPD 患者启动系统性皮质类固醇治疗提供价值。

伦理与传播

本研究已获得北京朝阳医院伦理委员会批准(批准号:2020-KE-544),主要结果和次要结果将发表在同行评议期刊上。

试验注册号

NCT05059873。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6a3/10230870/0209e1acae58/bmjopen-2022-066354f01.jpg

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