A randomized trial comparing the Ambu (R) Aura-i (TM) with the air-Q (TM) intubating laryngeal airway as conduits for tracheal intubation in children

作者：Jagannathan Narasimhan^*; Sohn Lisa E; Sawardekar Amod; Gordon Jason; Shah Ravi D; Mukherji Isabella I; Roth Andrew G; Suresh Santhanam

来源：Paediatric Anaesthesia, 2012, 22(12): 1197-1204.

DOI：10.1111/pan.12024

• airway devices
• clinical trials
• laryngeal mask airway
• air-Q

Objectives To assess the clinical performance of the Ambu Aura-i (Aura-i) in children. Aim To compare the Aura-i with the air-Q intubating laryngeal airway (air-Q) for the purposes of fiberoptic-guided tracheal intubation. Background The Aura-i is a new supraglottic airway designed for tracheal intubation.
Materials/Methods One hundred twenty children, ages 1 month to 6 years, were randomized to receive either the Aura-i or air-Q, and divided into three equal subgroups (Group 1, 2, 3) based on weight. The time for successful tracheal intubation was primarily assessed. The ease, time, and number of attempts for successful device insertion, leak pressures, fiberoptic grade of laryngeal view, number of attempts time for removal of the device after tracheal intubation, and complications were secondarily assessed.
Results Device placement, tracheal intubation, and removal after tracheal intubation were successful in all patients. There were no differences in the time to successful tracheal intubation through the Aura-i (32.9 +/- 13.3 s), and the air-Q (33.9 +/- 13 s; P = 0.68), or fiberoptic grade of view between devices. There was not a statistically significant correlation between the time to intubation and the fiberoptic grade of laryngeal view in any of the groups. There were no statistically significant differences in the overall leak pressures, air-Q (18.3 +/- 6.1 cm H2O) vs Aura-i (16 +/- 5.1 cm H2O; P = 0.05). In Group 1 (510 kg), leak pressures were higher with the air-Q (23.4 +/- 7.2 cm H2O) than the Aura-i (16.1 +/- 5.2 cm H2O; P = 0.001). There were no statistically significant differences in the time for removal between the two devices (P = 0.11). However, with the size 1.5 Aura-i, the pilot balloon of the tracheal tube was removed in order to facilitate the removal of the device after tracheal intubation.
Conclusions Both devices served as effective conduits for fiberoptic-guided tracheal intubation. The limitation of the narrower proximal airway tube of the size 1.5 Aura-i should be considered if cuffed tracheal tubes are to be utilized.

• 出版日期2012-12
• 单位西北大学