The distance between the glottis and the cuff of a tracheal tube placed through three supraglottic airway devices in children: A randomised controlled trial

Eur J Anaesthesiol. 2019 Oct;36(10):721-727. doi: 10.1097/EJA.0000000000001070.

Abstract

Background: After tracheal tube insertion via various types of supraglottic airway devices, the distance from the tube cuff to the vocal cords has not been evaluated in children.

Objectives: The aim of this study was to evaluate the position of a tracheal tube cuff relative to the glottis in children when one of three supraglottic airway devices (I-gel, AuraGain and air-Q laryngeal airway) are used as intubation conduits.

Design: A randomised controlled trial.

Setting: Tertiary children's hospital.

Patients: Children aged less than 7 years.

Intervention: In vivo fibre-optic assessment and in vitro measurement.

Main outcome measures: The main outcome was the safety margin: the distance between the ventilation outlet of the supraglottic airway device and the beginning of the proximal cuff minus that from the ventilation outlet to the glottis. The maximum inner diameter of the cuffed tracheal tube that could be inserted, the fibre-optic view score and the oropharyngeal leak pressure were also evaluated.

Results: The three devices exhibited significant differences in the distance from the ventilation outlet to the glottis (mean ± SD): I-gel 3.6 ± 0.6 cm, AuraGain 3.8 ± 0.7 cm, air-Q 2.8 ± 1.0 cm (P < 0.001). The safety margin was greatest with the air-Q and narrowest with the I-gel: I gel 1.9 ± 1.1 cm, AuraGain 4.4 ± 0.7 cm and air-Q 7.9 ± 1.1 cm. Using the AuraGain and air-Q, the cuffs of the tracheal tubes were predicted to be located below the glottis with one-size and two-size smaller tracheal tubes in all patients. However, using I-gel, the cuffs would be below the glottis in 69% (95% CI 49.6 to 84.5) and 29% (95% CI 14.0 to 48.4) of the patients with a one-size and two-size smaller tube, respectively.

Conclusion: The AuraGain and air-Q are well tolerated intubating conduits. The possibility of vocal cord damage is higher when the I-gel is used.

Trial registration: www.clinicaltrials.gov (number: NCT03156166).

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Airway Management / instrumentation*
  • Anesthesia, General / instrumentation
  • Child
  • Child, Preschool
  • Female
  • Fiber Optic Technology
  • Glottis / anatomy & histology*
  • Hospitals, Pediatric
  • Humans
  • Infant
  • Intubation, Intratracheal / instrumentation*
  • Laryngeal Masks / adverse effects*
  • Male
  • Patient Safety
  • Respiration, Artificial / methods*
  • Tertiary Care Centers
  • Trachea / anatomy & histology*
  • Treatment Outcome

Associated data

  • ClinicalTrials.gov/NCT03156166