Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Poitiers, Poitiers, France
Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Poitiers, Poitiers, France.
BMJ Open. 2024 Oct 23;14(10):e083232. doi: 10.1136/bmjopen-2023-083232.
First-line oxygenation strategy in patients with acute hypoxaemic respiratory failure consists in standard oxygen or high-flow nasal oxygen therapy. Clinical practice guidelines suggest the use of high-flow nasal oxygen rather than standard oxygen. However, findings remain contradictory with a low level of certainty. We hypothesise that compared with standard oxygen, high-flow nasal oxygen may reduce mortality in patients with acute hypoxaemic respiratory failure.
The Standard Oxygen versus High-flow nasal Oxygen-trial is an investigator-initiated, multicentre, open-label, randomised controlled trial comparing high-flow nasal oxygen versus standard oxygen in patients admitted to an intensive care unit (ICU) for acute respiratory failure with moderate-to-severe hypoxaemia. 1110 patients will be randomly assigned to one of the two groups with a ratio of 1:1. The primary outcome is the number of patients who died 28 days after randomisation. Secondary outcomes include comfort, dyspnoea and oxygenation 1 hour after treatment initiation, the number of patients intubated at day 28, mortality in ICU, in hospital and until day 90, and complications during ICU stay.
The study has been approved by the central Ethics Committee 'Sud Méditerranée III' (2020-07-05) and patients will be included after informed consent. The results will be submitted for publication in peer-reviewed journals.
NCT04468126.
急性低氧性呼吸衰竭患者的一线氧疗策略包括标准氧疗或高流量鼻氧疗。临床实践指南建议使用高流量鼻氧疗而非标准氧疗。然而,研究结果仍存在矛盾,证据确定性水平较低。我们假设与标准氧疗相比,高流量鼻氧疗可能降低急性低氧性呼吸衰竭患者的死亡率。
标准氧与高流量鼻氧疗试验是一项由研究者发起的、多中心、开放标签、随机对照试验,旨在比较急性呼吸衰竭伴中重度低氧血症患者入住重症监护病房(ICU)时接受高流量鼻氧疗与标准氧疗的效果。将 1110 例患者随机分为两组,比例为 1:1。主要结局为随机分组后 28 天死亡的患者人数。次要结局包括治疗开始后 1 小时的舒适度、呼吸困难和氧合情况、第 28 天插管的患者人数、ICU 内、院内和第 90 天的死亡率以及 ICU 期间的并发症。
该研究已获得“南地中海 III 区”中央伦理委员会的批准(2020-07-05),并在获得知情同意后纳入患者。研究结果将提交给同行评议的期刊发表。
NCT04468126。