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在资源有限的环境下,成人急性低氧性呼吸衰竭时使用标准低流量氧疗、高流量氧疗或持续气道正压通气进行呼吸支持:一项随机、开放标签、临床试验的方案 - 非洲急性呼吸干预研究(ARISE-AFRICA)。

Respiratory support with standard low-flow oxygen therapy, high-flow oxygen therapy or continuous positive airway pressure in adults with acute hypoxaemic respiratory failure in a resource-limited setting: protocol for a randomised, open-label, clinical trial - the Acute Respiratory Intervention StudiEs in Africa (ARISE-AFRICA) study.

机构信息

Department of Anaesthesia and Critical Care, Makerere University College of Health Sciences, Kampala, Uganda

Department of Anaesthesia and Critical Care, Makerere University College of Health Sciences, Kampala, Uganda.

出版信息

BMJ Open. 2024 Jul 1;14(6):e082223. doi: 10.1136/bmjopen-2023-082223.

Abstract

RATIONALE

Acute hypoxaemic respiratory failure (AHRF) is associated with high mortality in sub-Saharan Africa. This is at least in part due to critical care-related resource constraints including limited access to invasive mechanical ventilation and/or highly skilled acute care workers. Continuous positive airway pressure (CPAP) and high-flow oxygen by nasal cannula (HFNC) may prove useful to reduce intubation, and therefore, improve survival outcomes among critically ill patients, particularly in resource-limited settings, but data in such settings are lacking. The aim of this study is to determine whether CPAP or HFNC as compared with standard oxygen therapy, could reduce mortality among adults presenting with AHRF in a resource-limited setting.

METHODS

This is a prospective, multicentre, randomised, controlled, stepped wedge trial, in which patients presenting with AHRF in Uganda will be randomly assigned to standard oxygen therapy delivered through a face mask, HFNC oxygen or CPAP. The primary outcome is all-cause mortality at 28 days. Secondary outcomes include the number of patients with criteria for intubation at day 7, the number of patients intubated at day 28, ventilator-free days at day 28 and tolerance of each respiratory support.

ETHICS AND DISSEMINATION

The study has obtained ethical approval from the Research and Ethics Committee, School of Biomedical Sciences, College of Health Sciences, Makerere University as well as the Uganda National Council for Science and Technology. Patients will be included after informed consent. The results will be submitted for publication in peer-reviewed journals.

TRIAL REGISTRATION NUMBER

NCT04693403.

PROTOCOL VERSION

8 September 2023; version 5.

摘要

背景

急性低氧性呼吸衰竭(AHRF)与撒哈拉以南非洲的高死亡率相关。这至少部分归因于与重症监护相关的资源限制,包括有限的有创机械通气和/或高技能的急性护理人员的获取。持续气道正压通气(CPAP)和高流量鼻导管给氧(HFNC)可能有助于减少插管,从而改善重症患者的生存结局,特别是在资源有限的环境中,但此类环境中缺乏相关数据。本研究旨在确定 CPAP 或 HFNC 与标准氧疗相比,是否可以降低资源有限环境中出现 AHRF 的成人患者的死亡率。

方法

这是一项前瞻性、多中心、随机、对照、阶梯式楔形试验,乌干达出现 AHRF 的患者将被随机分配接受标准氧疗(通过面罩输送)、HFNC 氧疗或 CPAP。主要结局是 28 天的全因死亡率。次要结局包括第 7 天符合插管标准的患者人数、第 28 天插管的患者人数、第 28 天的无呼吸机天数以及每种呼吸支持方式的耐受性。

伦理与传播

该研究已获得乌干达马凯雷雷大学医学院生物医学科学学院研究和伦理委员会以及乌干达科学技术委员会的伦理批准。患者将在获得知情同意后纳入研究。研究结果将提交给同行评审期刊发表。

试验注册号

NCT04693403。

方案版本

2023 年 9 月 8 日;第 5 版。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/481e/11218023/cdf874eac1a1/bmjopen-2023-082223f01.jpg

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