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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
- 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.
- Subjects :
- medicine.medical_specialty
high-flow nasal cannula
medicine.medical_treatment
[SDV]Life Sciences [q-bio]
Nose
medicine.disease_cause
anticipated difficult intubation
Anaesthesia
03 medical and health sciences
0302 clinical medicine
030202 anesthesiology
Informed consent
Intensive care
fiberoptic intubation
Protocol
Cannula
Humans
Medicine
Intubation
Prospective Studies
Airway Management
Randomized Controlled Trials as Topic
Protocol (science)
business.industry
Masks
Oxygen Inhalation Therapy
General Medicine
Oxygenation
3. Good health
video-laryngoscopy
[SDV] Life Sciences [q-bio]
Single centre
030228 respiratory system
Research Design
Emergency medicine
apneic oxygenation
Airway management
business
Nasal cannula
Subjects
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⟩