PT  - JOURNAL ARTICLE
AU  - Jean-Pierre Frat
AU  - Jean-Damien Ricard
AU  - Rémi Coudroy
AU  - René Robert
AU  - Stéphanie Ragot
AU  - Arnaud W Thille
ED  - ,
TI  - Preoxygenation with non-invasive ventilation versus high-flow nasal cannula oxygen therapy for intubation of patients with acute hypoxaemic respiratory failure in ICU: the prospective randomised controlled FLORALI-2 study protocol
AID  - 10.1136/bmjopen-2017-018611
DP  - 2017 Dec 01
TA  - BMJ Open
PG  - e018611
VI  - 7
IP  - 12
4099  - http://bmjopen.bmj.com/content/7/12/e018611.short
4100  - http://bmjopen.bmj.com/content/7/12/e018611.full
SO  - BMJ Open2017 Dec 01; 7
AB  - Introduction Endotracheal intubation in intensive care unit (ICU) is a procedure at high risk of life-threatening complications. Among them, severe oxygen desaturation, usually defined as a drop of pulse oxymetry (SpO2) below 80%, is the most common. Preoxygenation enables delaying oxygen desaturation occurring during apnea induced by anaesthetic drugs. Data suggest that non-invasive ventilation (NIV) or high-flow nasal cannula (HFNC) oxygen therapy could further increase PaO2 before intubation procedure and prevent oxygen desaturation episodes as compared with standard oxygen. However, no recommendation favours one technique rather than the other, since they have never been compared. Hence, whether a strategy of preoxygenation with NIV or HFNC is more effective than the other in patients with acute hypoxaemic respiratory failure remains to be established.Methods and analysis The FLORALI-2 study is a multicentre randomised controlled trial comparing a preoxygenation strategy with either NIV or HFNC in patients with acute hypoxaemic respiratory failure needing intubation in ICU. The 320 patients will be randomised with a ratio 1:1 in two groups according to the strategy of preoxygenation. The primary outcome is the occurrence of an episode of severe oxygen desaturation defined by a drop of SpO2 below 80% during the intubation procedure. Secondary outcomes include feasibility of the two strategies, immediate and late complications related to intubation.Ethics and dissemination The study has been approved by the central ethics committee (Ethics Committee Ouest-III, Poitiers, France) and patients will be included after informed consent. The results will be submitted for publication in peer-reviewed journals.Trial registration number NCT02668458; Pre-results.