Jaber Samir, Molinari Nicolas, De Jong Audrey
Department of Anaesthesiology and Critical Care Medicine B (DAR B), Saint-Eloi Hospital, University Teaching Hospital of Montpellier, Montpellier, France INSERM U1046, Montpellier, France.
Department of Statistics, University of Montpellier Lapeyronie Hospital, UMR 729 MISTEA, Montpellier, France.
BMJ Open. 2016 Aug 12;6(8):e011298. doi: 10.1136/bmjopen-2016-011298.
Tracheal intubation in the intensive care unit (ICU) is associated with severe life-threatening complications including severe hypoxaemia. Preoxygenation before intubation has been recommended in order to decrease such complications. Non-invasive ventilation (NIV)-assisted preoxygenation allows increased oxygen saturation during the intubation procedure, by applying a positive end-expiratory pressure (PEEP) to prevent alveolar derecruitment. However, the NIV mask has to be taken off after preoxygenation to allow the passage of the tube through the mouth. The patient with hypoxaemia does not receive oxygen during this period, at risk of major hypoxaemia. High-flow nasal cannula oxygen therapy (HFNC) has a potential for apnoeic oxygenation during the apnoea period following the preoxygenation with NIV. Whether application of HFNC combined with NIV is more effective at reducing oxygen desaturation during the intubation procedure compared with NIV alone for preoxygenation in patients with hypoxaemia in the ICU with acute respiratory failure remains to be established.
The HFNC combined to NIV for decreasing oxygen desaturation during the intubation procedure in patients with hypoxaemia in the ICU (OPTINIV) trial is an investigator-initiated monocentre randomised controlled two-arm trial with assessor-blinded outcome assessment. The OPTINIV trial randomises 50 patients with hypoxaemia requiring orotracheal intubation for acute respiratory failure to receive NIV (pressure support=10, PEEP=5, fractional inspired oxygen (FiO2)=100%) combined with HFNC (flow=60 L/min, FiO2=100%, interventional group) or NIV alone (reference group) for preoxygenation. The primary outcome is lowest oxygen saturation during the intubation procedure. Secondary outcomes are intubation-related complications, quality of preoxygenation and ICU mortality.
The study project has been approved by the appropriate ethics committee (CPP Sud-Méditerranée). Informed consent is required. If combined application of HFNC and NIV for preoxygenation of patients with hypoxaemia in the ICU proves superior to NIV preoxygenation, its use will become standard practice, thereby decreasing hypoxaemia during the intubation procedure and potential complications related to intubation.
NCT02530957.
重症监护病房(ICU)中的气管插管与包括严重低氧血症在内的严重危及生命的并发症相关。为了减少此类并发症,建议在插管前进行预充氧。无创通气(NIV)辅助预充氧通过应用呼气末正压(PEEP)防止肺泡萎陷,从而在插管过程中提高氧饱和度。然而,预充氧后必须取下NIV面罩,以便气管导管经口腔插入。在此期间,低氧血症患者无法吸氧,存在严重低氧血症的风险。高流量鼻导管给氧疗法(HFNC)在NIV预充氧后的呼吸暂停期间具有进行无氧自主呼吸给氧的潜力。对于ICU中患有急性呼吸衰竭的低氧血症患者,与单独使用NIV进行预充氧相比,联合应用HFNC和NIV在插管过程中降低氧饱和度是否更有效仍有待确定。
ICU中低氧血症患者插管过程中联合应用HFNC降低氧饱和度(OPTINIV)试验是一项由研究者发起的单中心随机对照双臂试验,采用盲法评估结局。OPTINIV试验将50例因急性呼吸衰竭需要经口气管插管的低氧血症患者随机分为两组,分别接受NIV(压力支持=10,PEEP=5,吸入氧分数(FiO2)=100%)联合HFNC(流量=60 L/min,FiO2=100%,干预组)或单独使用NIV(对照组)进行预充氧。主要结局是插管过程中的最低氧饱和度。次要结局包括插管相关并发症、预充氧质量和ICU死亡率。
本研究项目已获得适当的伦理委员会(地中海地区南部保护个人委员会)批准。需要获得知情同意。如果在ICU中对低氧血症患者联合应用HFNC和NIV进行预充氧被证明优于单独使用NIV预充氧,其应用将成为标准做法,从而减少插管过程中的低氧血症以及与插管相关的潜在并发症。
NCT02530957。