• Eur J Anaesthesiol · Apr 2016

    Randomized Controlled Trial

    Low-positive pressure ventilation improves non-hypoxaemic apnoea tolerance during ear, nose and throat pan-endoscopy: A prospective randomised controlled trial.

    • Osama Abou-Arab, Pierre-Grégoire Guinot, Evgeny Dimov, Momar Diouf, Bruno de Broca, Aurélie Biet, Rody Zaatar, Eugénie Bernard, Hervé Dupont, and Emmanuel Lorne.
    • From the Anaesthesiology and Critical Care Department, Amiens University Hospital, Place Victor Pauchet (OAA, PGG, BDB, EB, HD, EL); INSERM U1088, Jules Verne University of Picardy, Amiens (PGG, HD, EL); C... more linique Sainte Isabelle, Route d'Amiens, Abbeville (ED); Centre de Recherche Clinique CHU Amiens (MD); and ENT Surgery Department, Amiens University Hospital, Place Victor Pauchet, Amiens, France (AB, RZ). less
    • Eur J Anaesthesiol. 2016 Apr 1; 33 (4): 269-74.

    BackgroundIt has been suggested that oxygenation using pressure support ventilation (PSV) before general anaesthesia can reduce the duration of non-hypoxaemic apnoea.ObjectiveThe objective was to determine whether or not pre-oxygenation with PSV increases the duration of non-hypoxaemic apnoea in non-obese patients during pan-endoscopy.DesignA randomised, controlled trial.SettingAmiens University Hospital, France.PatientsFifty patients scheduled for ENT pan-endoscopy with a BMI lower than 35  kg  m(-2).InterventionPatients scheduled for pan-endoscopy were enrolled to receive either 100% oxygen at neutral pressure (the control group) or 100% oxygen with positive-pressure ventilation (a positive inspiratory pressure of 4  cmH2O and a positive end-expiratory pressure of 4  cmH2O; the PSV group) during spontaneous ventilation with a face mask. The goal of pre-oxygenation was to obtain an end-tidal oxygen concentration of more than 90% prior to induction of anaesthesia.Main Outcome MeasuresThe primary efficacy criterion was the duration of non-hypoxaemic apnoea (i.e. before the peripheral capillary oxygen saturation fell to 90%). Secondary outcomes were duration of pre-oxygenation, pre-oxygenation failure and tolerance.ResultsThe mean (interquartile range) duration of non-hypoxaemic apnoea was longer in the PSV group [598 (447 to 717) s] than in the control group [310 (217 to 451) s] (P < 0.001). Oxygenation time was shorter in the PSV group [190 (159 to 225) s] than in the control group [245 (151 to 435) s] (P = 0.037). Pre-oxygenation was unsuccessful (i.e. end-tidal oxygen concentration was < 90%) in 20% of the patients in the control group but none in the PSV group. The intergroup difference in the duration of pan-endoscopy was not significant. Tolerance was good or very good in all patients.ConclusionOur results show that pre-oxygenation with PSV is associated with a longer duration of non-hypoxaemic apnoea and a lower frequency of manual reventilation during ENT pan-endoscopy. CLINICALTRIALS.Gov Registration NumberNCT02167334.

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