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

Eur J Anaesthesiol. 2016 Apr;33(4):269-74. doi: 10.1097/EJA.0000000000000394.

Abstract

Background: It has been suggested that oxygenation using pressure support ventilation (PSV) before general anaesthesia can reduce the duration of non-hypoxaemic apnoea.

Objective: The 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.

Design: A randomised, controlled trial.

Setting: Amiens University Hospital, France.

Patients: Fifty patients scheduled for ENT pan-endoscopy with a BMI lower than 35 kg m(-2).

Intervention: Patients 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 measures: The 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.

Results: The 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.

Conclusion: Our 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 number: NCT02167334.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Anesthesia, General
  • Apnea / diagnosis
  • Apnea / etiology
  • Apnea / prevention & control*
  • Female
  • France
  • Hospitals, University
  • Humans
  • Hypoxia / diagnosis
  • Hypoxia / etiology
  • Hypoxia / prevention & control*
  • Laryngeal Masks
  • Laryngoscopy* / adverse effects
  • Male
  • Middle Aged
  • Otorhinolaryngologic Surgical Procedures / adverse effects
  • Otorhinolaryngologic Surgical Procedures / methods*
  • Positive-Pressure Respiration / adverse effects
  • Positive-Pressure Respiration / instrumentation
  • Positive-Pressure Respiration / methods*
  • Time Factors
  • Treatment Outcome

Associated data

  • ClinicalTrials.gov/NCT02167334