Apnoeic oxygenation in morbid obesity: a randomised controlled trial comparing facemask and high-flow nasal oxygen delivery

John Schutzer-Weissmann, Thomas Wojcikiewicz, Anil Karmali, Asta Lukosiute, Ruoyi Sun, Rafiq Kanji, Ahmed R Ahmed, Sanjay Purkayastha, Stephen J Brett, Jonathan Cousins, John Schutzer-Weissmann, Thomas Wojcikiewicz, Anil Karmali, Asta Lukosiute, Ruoyi Sun, Rafiq Kanji, Ahmed R Ahmed, Sanjay Purkayastha, Stephen J Brett, Jonathan Cousins

Abstract

Background: Obesity is a risk factor for airway-related incidents during anaesthesia. High-flow nasal oxygen has been advocated to improve safety in high-risk groups, but its effectiveness in the obese population is uncertain. This study compared the effect of high-flow nasal oxygen and low-flow facemask oxygen delivery on duration of apnoea in morbidly obese patients.

Methods: Morbidly obese patients undergoing bariatric surgery were randomly allocated to receive either high-flow nasal (70 L min-1) or facemask (15 L min-1) oxygen. After induction of anaesthesia, the patients were apnoeic for 18 min or until peripheral oxygen saturation decreased to 92%.

Results: Eighty patients were studied (41 High-Flow Nasal Oxygen, 39 Facemask). The median apnoea time was 18 min in both the High-Flow Nasal Oxygen (IQR 18-18 min) and the Facemask (inter-quartile range [IQR], 4.1-18 min) groups. Five patients in the High-Flow Nasal Oxygen group and 14 patients in the Facemask group desaturated to 92% within 18 min. The risk of desaturation was significantly lower in the High-Flow Nasal Oxygen group (hazard ratio=0.27; 95% confidence interval [CI], 0.11-0.65; P=0.007).

Conclusions: In experienced hands, apnoeic oxygenation is possible in morbidly obese patients, and oxygen desaturation did not occur for 18 min in the majority of patients, whether oxygen delivery was high-flow nasal or low-flow facemask. High-flow nasal oxygen may reduce desaturation risk compared with facemask oxygen. Desaturation risk is a more clinically relevant outcome than duration of apnoea. Individual physiological factors are likely to be the primary determinant of risk rather than method of oxygen delivery.

Clinical trial registration: NCT03428256.

Keywords: THRIVE; apnoeic oxygenation; apnoeic ventilation; bariatric anaesthesia; desaturation risk; high-flow nasal oxygen; obesity; safe apnoea time.

Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.

Figures

Fig 1
Fig 1
CONSORT diagram. CONSORT, Consolidated Standards of Reporting Trials; HFNO, high-flow nasal oxygen.
Fig 2
Fig 2
Risk of desaturation during apnoea. Proportion of study participants in HFNO (purple line) and FM (blue line) groups with oxygen saturation >92% during apnoea. Hazard ratio comparing FM and HFNO groups, 0.27 (95% confidence interval, 0.11–0.65; log-rank P=0.007). TA, onset of apnoea. TA+x, apnoea duration where x denotes min after TA; FM, facemask oxygen; HFNO, high-flow nasal oxygen.
Fig 3
Fig 3
Pao2 and Paco2 change over time during apnoea. Change in arterial oxygen and carbon dioxide tension during apnoea. TA, onset of apnoea; TA+x, apnoea duration where x denotes min after TA. Each line represents an individual participant (purple: high flow nasal oxygen group; blue: facemask group). Light lines represent participants whose oxygen saturation level remained >92% during apnoea throughout the 18 min period. Dark lines represent participants who desaturated to 92% during the study period.

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Source: PubMed

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