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Apr 30, 2013Article Details
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A study to evaluate fibreoptic-guided intubation through the i-gel
Abstract
Objective: The i-gel™ superglottic airway (Intersurgical, Berkshire, UK) has been reported to function as an airway rescue device and as a conduit for fibre-optic intubation in predicted difficult airways. The wider and shorter stem of the i-gel™ and the absence of a grille at the distal end suggests that it may serve as an ideal channel for intubation using a fibrescope. The aim of this prospective study was to determine the feasibility of using fibreoptic-guided intubation through an i-gel™ airway in adult patients undergoing elective surgery.
Design: A prospective clinical study.
Subjects and setting: Sixty patients of both genders, aged 18-60 years, who presented for elective surgery in a tertiary care centre, were enrolled in the study.
Outcome measures: The number of insertion attempts, ease of insertion and insertion time of the i-gel™, fibreoptic view through the i-gel™ tube, airway seal pressure, ease of tracheal tube placement with the help of a fibreoptic bronchoscope through the i-gel™, time taken for tracheal tube placement and any evidence of airway injury, were determined.
Results: Successful insertion of the i-gel™ was achieved in 96.66% of patients. The mean time of insertion of the i-gel™ was 9.09 ± 4.17 seconds. Ease of tracheal tube placement via the i-gel™ was found to be easy in 91.4% of cases. The mean total tracheal tube placement time through the i-gel™ was recorded as 89.16 ± 8.29 seconds.
Conclusion: The i-gel™ was easy to insert, with a good first attempt success rate and acceptable insertion time. The success rate for fibreoptic-guided intubation through the i-gel™ was also acceptable. Hence it can serve as an alternative conduit for fibreoptic-guided intubation.
Design: A prospective clinical study.
Subjects and setting: Sixty patients of both genders, aged 18-60 years, who presented for elective surgery in a tertiary care centre, were enrolled in the study.
Outcome measures: The number of insertion attempts, ease of insertion and insertion time of the i-gel™, fibreoptic view through the i-gel™ tube, airway seal pressure, ease of tracheal tube placement with the help of a fibreoptic bronchoscope through the i-gel™, time taken for tracheal tube placement and any evidence of airway injury, were determined.
Results: Successful insertion of the i-gel™ was achieved in 96.66% of patients. The mean time of insertion of the i-gel™ was 9.09 ± 4.17 seconds. Ease of tracheal tube placement via the i-gel™ was found to be easy in 91.4% of cases. The mean total tracheal tube placement time through the i-gel™ was recorded as 89.16 ± 8.29 seconds.
Conclusion: The i-gel™ was easy to insert, with a good first attempt success rate and acceptable insertion time. The success rate for fibreoptic-guided intubation through the i-gel™ was also acceptable. Hence it can serve as an alternative conduit for fibreoptic-guided intubation.
