Ricard Jean-Damien, Dib Fadia, Esposito-Farese Marina, Messika Jonathan, Girault Christophe
Service de Réanimation Médico-Chirurgicale, AP-HP, Hôpital Louis Mourier, Colombes, France.
INSERM, IAME, UMR 1137, Paris, France.
BMJ Open. 2018 Sep 19;8(9):e022983. doi: 10.1136/bmjopen-2018-022983.
This study protocol describes a trial designed to investigate whether high-flow heated and humidified nasal oxygen (HFHO) therapy in patients with hypercapnic acute respiratory failure (ARF) reduces the need of non-invasive ventilation (NIV).
This is an open-label, superiority, international, parallel-group, multicentre randomised controlled two-arm trial, with an internal feasibility pilot phase. 242 patients with hypercapnic ARF requiring NIV admitted to an intensive care unit, an intermediate care or a respiratory care unit will be randomised in a 1:1 ratio to receive HFHO or standard oxygen in between NIV sessions. Randomisation will be centralised and stratified by centre and pH at admission (pH ≤7.25 or >7.25). The primary outcome will be the number of ventilator-free days (VFDs) and alive at day 28 postrandomisation. The secondary outcomes will encompass parameters related to the VFDs, comfort and tolerance variables, hospital length of stay and mortality. VFDs at 28 days postrandomisation will be compared between the two groups by Wilcoxon-Mann-Whitney two-sample rank-sum test in the intention-to-treat population. A sensitivity analysis will be conducted in the population of patients for whom the criteria of switching from NIV to spontaneous breathing, or conversely, are not strictly verified.
The protocol has been approved by the (CPP) (ref CPP17-049a/2017-A01830-53) and will be carried out in accordance with the Declaration of Helsinki and Good Clinical Practice guidelines. A trial steering committee will oversee the progress of the study. Findings will be disseminated through national and international scientific conferences, and publication in peer-reviewed journals.
NCT03406572.
本研究方案描述了一项试验,旨在调查高流量加热湿化鼻导管吸氧(HFHO)疗法对高碳酸血症急性呼吸衰竭(ARF)患者是否能减少无创通气(NIV)的需求。
这是一项开放标签、优效性、国际性、平行组、多中心随机对照双臂试验,设有内部可行性预试验阶段。242例入住重症监护病房、中级护理病房或呼吸护理病房且需要无创通气的高碳酸血症急性呼吸衰竭患者将按1:1比例随机分组,在无创通气间隙接受高流量加热湿化鼻导管吸氧或标准吸氧。随机分组将由中心集中进行,并按中心和入院时的pH值(pH≤7.25或>7.25)进行分层。主要结局将是随机分组后第28天无呼吸机天数(VFDs)且存活。次要结局将包括与无呼吸机天数、舒适度和耐受性变量、住院时间及死亡率相关的参数。在意向性分析人群中,采用Wilcoxon-Mann-Whitney两样本秩和检验比较两组随机分组后28天的无呼吸机天数。将在未严格验证从无创通气转换为自主呼吸或相反转换标准的患者人群中进行敏感性分析。
本方案已获得(CPP)批准(参考编号CPP17 - 049a/2017 - A01830 - 53),并将按照《赫尔辛基宣言》和《良好临床实践指南》开展。试验指导委员会将监督研究进展。研究结果将通过国内和国际科学会议进行传播,并发表在同行评审期刊上。
NCT03406572。