None listed
Conditions
Brief summary
Airway or respiratory complication is one of leading causes of morbidity and mortality in anaesthesia. There are different techniques and intubating equipment (laryngoscope) available for anaesthetists to deal with difficult airways. Anaesthetists use their knowledge and previous experience to decide which type of laryngoscope to use in these cases. In this study, we are evaluating, for the first time, this newly available videolaryngoscope. It requires a technique called "indirect laryngoscopy". We are comparing it with the standard direct laryngoscopy by using the Macintosh blade. We hypothesise that In simulated difficult airways, the novel videolaryngoscope achieve a better laryngoscopy view as compared to the Macintosh blade. We will prospectively recruit 30 voluntary anaesthetic residents, registrars or consultants for this study. All participants will be tested on using each of the two intubation devices on a manikin with a simulated difficult airway. Participants will be assigned to one of the two groups – Group 1: novel videolaryngoscope followed by Macintosh laryngoscope, or Group 2: Macintosh laryngoscope followed by novel videolaryngoscope. The primary outcome is the best laryngoscopy view achieved. Secondary outcomes include: • The time taken for successful tracheal intubation. • Number of failed intubation. • Number of intubation attempts. • Number and type of intubating adjuncts used. • The ease of intubation, which will be surveyed using a visual analogue scale from 0-100mm.
Interventions
We are comparing the effectiveness of a newly available video laryngoscope with the standard direct laryngoscopy by using the Macintosh blade in performing endotracheal intubation in a manikin with simulated difficult airway. Each participant will receive standardized instruction for the use of each device as per the manufacturer’s guidelines before the commencement of the study. All participants will be tested on using each of the two intubation devices on a manikin with a simulated difficult airway. Participants will be assigned to one of the two groups – Group 1: novel videolaryngoscope followed by Macintosh laryngoscope, or Group 2: Macintosh laryngoscope followed by novel videolaryngoscope. The intervention will be delivered once only in both groups. Intervention fidelity will not be assessed but participants will be observed directly while using the new device. There will not be any wash-out period between the time when the control device is used and the time when the intervention device is used.
Sponsors
Study design
Eligibility
Inclusion criteria
Anaesthetic residents, registrars or consultants who work at the Royal Melbourne Hospital
Exclusion criteria
No exclusion criteria