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The effect of transnasal humidified rapid-insufflation ventilator exchange (THRIVE) versus nasal prongs on safe apnoea time in paralysed obese patients: a randomised controlled trial.

Authors :
Guy L
Christensen R
Dodd B
Pelecanos A
Wyssusek K
Van Zundert A
Eley VA
Source :
British journal of anaesthesia [Br J Anaesth] 2022 Feb; Vol. 128 (2), pp. 375-381. Date of Electronic Publication: 2021 Dec 08.
Publication Year :
2022

Abstract

Background: Evidence is lacking regarding the efficacy of Optiflow transnasal humidified rapid-insufflation ventilator exchange (THRIVE™) in obese patients. We compared the impact of this technique at 70 L min <superscript>-1</superscript> with 4 L min <superscript>-1</superscript> oxygen via nasal prongs on safe apnoea times of paralysed obese patients.<br />Methods: We randomised adults with a BMI >35 kg m <superscript>-2</superscript> undergoing elective bariatric surgery. While apnoeic and paralysed, Group T received 70 L min <superscript>-1</superscript> oxygen via Optiflow THRIVE™. Group N received nasal prong oxygen at 4 L min <superscript>-1</superscript> . The primary outcome was time to SpO <subscript>2</subscript> ≤95% while apnoeic, with a 360 s cut-off. This was analysed by applying a time-to-event analysis.<br />Results: Forty-two patients were included. The median (inter-quartile range) BMI was 44.8 kg m <superscript>-2</superscript> (40.0-50.0) in Group T and 42.0 kg m <superscript>-2</superscript> (39.3-45.1) in Group N. Median (inter-quartile range) time to SpO <subscript>2</subscript> ≤95% in Group T was 356 (165 to ≥360) s and in Group N, 210 (160-270) s. Using a survival analysis framework, median time-to-event in Group T was 356 s (95% confidence interval 165 s-upper limit not defined) and 210 s (95% confidence interval 160-242 s) (P=0.049) in Group N.<br />Conclusions: Compared with oxygen delivered via nasal prongs at 4 L min <superscript>-1</superscript> , oxygen delivery via Optiflow THRIVE™ at a flow rate of 70 L min <superscript>-1</superscript> can prolong safe apnoea time, however, the results are statistically inconclusive. Optiflow THRIVE™ did decrease the rate of reduction in Pa <subscript>o2</subscript> during apnoea.<br />Clinical Trial Registration: ANZCTR 12618000445279.<br /> (Copyright © 2021 British Journal of Anaesthesia. Published by Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1471-6771
Volume :
128
Issue :
2
Database :
MEDLINE
Journal :
British journal of anaesthesia
Publication Type :
Academic Journal
Accession number :
34895717
Full Text :
https://doi.org/10.1016/j.bja.2021.10.048