Effectiveness of high-flow nasal cannula oxygen in apneic oxygenation during intubation in high-risk surgical patients: a systematic review protocol

Author:

Sekhar Praba12ORCID,Thiruvenkatarajan Venkatesan23,Sekhar Vimal123,van Wijk Roelof23,Barker Timothy12

Affiliation:

1. JBI, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, SA, Australia

2. The University of Adelaide, Adelaide, SA, Australia

3. Department of Anaesthesia, The Queen Elizabeth Hospital, Adelaide, SA, Australia

Abstract

Objective: This review will investigate the effectiveness of high-flow nasal oxygen in apneic oxygenation through safe apnea time and other ventilation parameters in patients at high risk of oxygen desaturation during induction and tracheal intubation for anesthesia management. Introduction: High-risk surgical patient groups include obese patients, those with suspected or known obstructive sleep apnea, and critically ill patients, who are at risk of rapid oxygen desaturation during intubation. Conventional oxygen administration in induction and intubation of patients undergoing general anesthesia include nasal cannulas, simple face masks, Venturi, buccal oxygenation, bag-valve mask ventilation, and non-invasive ventilation. High-flow nasal oxygen has emerged as a novel technique, and is advantageous because it increases positive end-expiratory pressure and oxygen delivered. Inclusion criteria: Eligible studies will include high-risk surgical patients aged 18 or above requiring endotracheal intubation in both emergency and elective anesthetic settings. High-risk patients are defined as those with suspected or known obstructive sleep apnea, obesity (BMI > 35), or critically ill patients (scored the American Society of Anesthesiologists classification as 3 or above). Methods: The review will follow the JBI methodology for systematic reviews of effectiveness. Databases to be searched include MEDLINE, Embase, and Scopus. Reference lists of selected studies will then be hand-searched for additional eligible studies. The primary outcome will be safe apnea time, with secondary outcomes including oxygen and carbon dioxide parameters, and adverse events (eg, gastric distension). Studies will, where possible, be pooled in statistical meta-analyses with data heterogeneity assessed using the standard χ 2 and I 2 tests. Review registration: PROSPERO CRD42022312145

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Nursing

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