Endotracheal Intubation
Conditions
Keywords
Fiberoptic intubation Training Simulation Performance
Brief summary
The aim of the study is to study whether training by residents or anesthesia assistants, on a recently introduced virtual-reality bronchoscopic simulator (ORSIM) improves performance of fiberoptic intubation in patients.
Detailed description
Traditionally, fiber optic bronchoscopy (FOB) intubation has been taught in a see one, do one basis. Modern training method in skill acquisition involves the use of simulators. Recently a portable, computer based, bronchoscopic simulator (ORSIM) was developed. The investigators hypothesized that operators trained with the ORSIM simulator will be more proficient in performing asleep FOB intubation than those trained with didactic teaching alone. This randomized trial involves 34 consented residents or anesthesia assistants (AAs). In preparation, each consented person will view a teaching video of FOB intubation and tips. They will then perform an asleep FOBI in the OR under a staff anesthesiologist's supervision who's familiar with the study. Those who are randomized to the ORSIM group with undergo simulator training of 30-60 min. Those in the Didactic group will not undergo further training. Within about a week, the resident/AA will perform another asleep FOB intubation. The study results will impact on how FOB intubation will be taught effectively in the future.
Interventions
The simulator/intervention group will undergo training on the virtual reality bronchoscopic simulator (ORSIM) for 60 minutes before the subjects perform the 2nd Fiber optic intubation
Sponsors
Study design
Eligibility
Inclusion criteria
Subject: * anesthesia/surgery/emergency/critical care residents or anesthesia assistants who have performed less than 5 Fiberoptic intubations
Exclusion criteria
* experience with bronchoscopy simulator or 5 or more FOB intubations Patient: * Anticipated difficult airway * Mallampati Grade (MPG) \>III * Body Mass Index (BMI) \>30
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Performance of Fiberoptic intubation assessed by validated 40 point Global Rating Scale (GRS) | 1 year |
Secondary
| Measure | Time frame |
|---|---|
| Success/Failure of Fiberoptic intubation | 1 year |
| The duration (in seconds) of the Fiberoptic intubation | 1 year |
Countries
Canada