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Preoxygenation in difficult airway management: high-flow oxygenation by nasal cannula versus face mask (the PREOPTIDAM study). Protocol for a single-centre randomised study

Authors :
Donatien Huard
Anne Chiffoleau
Samir Jaber
Fanny Feuillet
Melanie Tissot
Christophe Guitton
Karim Asehnoune
Mickael Vourc’h
Marielle Surbled
Arthur Guichoux
Gabrielle Baud
Centre hospitalier universitaire de Nantes (CHU Nantes)
Biostatistique, Recherche Clinique et Mesures Subjectives en Santé
Université de Nantes (UN)
Service Réanimation Médicale Polyvalente
Hôpital Saint-Jacques-Centre hospitalier universitaire de Nantes (CHU Nantes)
Centre Hospitalier Le Mans (CH Le Mans)
Physiologie & médecine expérimentale du Cœur et des Muscles [U 1046] (PhyMedExp)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)
Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)
Service d'anesthésie et réanimation chirurgicale [Nantes]
Hôtel-Dieu-Centre hospitalier universitaire de Nantes (CHU Nantes)
MORNET, Dominique
Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Source :
BMJ Open, BMJ Open, 2019, 9 (4), pp.e025909. ⟨10.1136/bmjopen-2018-025909⟩, BMJ Open, BMJ Publishing Group, 2019, 9 (4), pp.e025909. ⟨10.1136/bmjopen-2018-025909⟩
Publication Year :
2019
Publisher :
HAL CCSD, 2019.

Abstract

IntroductionAlthough preoxygenation and airway management respond to precise algorithms, difficult intubation (DI) remains a daily challenge in intensive care units and in the operating rooms because of its frequent complications, including hypoxaemia. To prevent desaturation during DI, high-flow oxygenation by nasal cannula (HFNC) could prove beneficial. Indeed, contrary to standard preoxygenation device, it can be held in place throughout the intubation trying to perform apnoeic oxygenation during DI. Hence, recent guidelines recommend HFNC during DI, but its relevance has never been evaluated in this setting in a large randomised study until now.Methods and analysisThe PREOPTIDAM trial is a prospective, single-centre, randomised, controlled study in Nantes University Hospital. In anticipated DI, we hypothesised that HFNC can decrease the incidence of desaturation ≤94% or face mask ventilation from 16% to 4% compared with standard device. Using a two-sided t-test with a first species risk of 5% and 80% power, a total of 186 patients will be included. Using a computer-generated randomisation, with a 1:1 allocation ratio, patients will be randomised to HFNC or face mask preoxygenation. Randomisation will be stratified on intubation sequence: Rapid sequence intubation or awake fibreoptic intubation. The primary objective is to determine whether HFNC is more efficient than standard oxygenation techniques to prevent desaturation ≤94% or face mask ventilation during DI. Intent-to-treat and per-protocol analysis are planned for the primary outcome.Ethics and disseminationThe study project has been approved by an independent ethics committee. Written informed consent will be obtained before study inclusion. Participant recruitment begins in September 2018. Results will be submitted to international peer-reviewed medical journals.Trial registration numberNCT03604120.

Details

Language :
English
ISSN :
20446055
Database :
OpenAIRE
Journal :
BMJ Open, BMJ Open, 2019, 9 (4), pp.e025909. ⟨10.1136/bmjopen-2018-025909⟩, BMJ Open, BMJ Publishing Group, 2019, 9 (4), pp.e025909. ⟨10.1136/bmjopen-2018-025909⟩
Accession number :
edsair.doi.dedup.....db02fcc4da0634e0212aed598fa369f9
Full Text :
https://doi.org/10.1136/bmjopen-2018-025909⟩