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Comparison of Two Airway Devices in Paediatric Patients With Difficult Airway

H

Hacettepe University

Status

Completed

Conditions

Intubation; Difficult or Failed

Treatments

Device: Glidescope
Device: Flexible fiberoptic bronchoscopy

Study type

Interventional

Funder types

Other

Identifiers

NCT06767995
HacettepeÜ-AR-BE-01

Details and patient eligibility

About

The aim of current study was to compare Flexible fiberoptic bronchoscopy (FFB) and Glidescope devices in terms of intubation success and duration of intubation in patients under 12 months of age with PRS. In the present study, the investigators found similar initial intubation success rates with Glidescope and FFB. Although further studies are needed to determine the superiority of the two techniques, the investigators believes that advanced airway techniques should be prioritized and can be safely used by reducing the number of interventions.

Full description

Flexible fiberoptic bronchoscopy (FFB) is considered the gold standard for airway management in both adult and pediatric patients with known or anticipated difficult airways. New generation videolaryngoscopy systems have also been successfully used as an alternative to FFB in pediatric patients with anticipated difficult airways. Airway management in patients with Pierre Robin Sequence (PRS) is challenging due to the classic triad of glossoptosis, micrognathia, and airway obstruction, along with potential accompanying syndromes and anomalies. It is clear that advanced airway techniques should be used in this patient group. However, there are not many studies in the literature demonstrating the success or superiority of these advanced airway techniques. The aim of current study was to compare FFB and Glidescope devices in terms of intubation success and duration of intubation in patients under 12 months of age with PRS. The current study is a prospective randomized controlled trial. Following ethical approval, between March 2021 and December 2023, intubation success and duration were compared between Flexible Intubation Video Endoscope (FIVE)® or GlideScope® Titanium devices in PRS patients under 12 months of age who underwent elective surgery under general anesthesia. Patients' anthropometric data such as age, weight, height, gender, preoperative airway examination measurements including mouth opening (MO), thyromental distance (TMD), frontal plane-chin distance (FPCD), and FPCD/weight index were recorded. Patients were randomized and intubated by two experienced faculty members using either FFB or Glidescope. Intubation success on the first attempt, intubation duration, glottic visualization time, and complications were recorded by a non-blinded research assistant. Both devices were compared for these parameters. The current study included 50 PRS patients, with 23 in the FFB group and 27 in the Glidescope group. There were no statistically significant differences between the two patient groups in terms of age, gender, anthropometric measurements, mouth opening, TMD, FPCD, and FPCD/weight index. There was no statistically significant difference in intubation success on the first attempt between the two groups (81.5% for Glidescope and 87% for FFB, p=0.430). The median intubation duration was statistically significantly shorter in the Glidescope group (35 seconds, IQR=10.5) compared to the FFB group (40 seconds, IQR=18) (p=0.032). Since the endotracheal tube passage times were similar in both groups, this difference was attributed to the time to achieve optimal glottic visualization. The median time to achieve optimal glottic visualization was 9.5 seconds (IQR=7.5) in the Glidescope group and 16 seconds (IQR=14) in the FFB group (p=0.002). However, the clinical significance of this difference cannot be conclusively determined. Moreover, complication rates during the procedure were similar between the two groups (18.5% for Glidescope and 13% for FFB, p=0.711). There is currently no validated test for predicting difficult preoperative airways in PRS patients. Literature reviews suggest that pediatric reference values for MO, TMD, and FPCD measurements are controversial, and more studies are needed to establish appropriate reference values. In the present study, the investigators found similar initial intubation success rates with Glidescope and FFB. Although further studies are needed to determine the superiority of the two techniques, the investigators believes that advanced airway techniques should be prioritized and can be safely used by reducing the number of interventions.

Enrollment

50 patients

Sex

All

Ages

1 day to 12 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Being under 12 months,
  • Being diagnosed with Pierre Robin Sequence,
  • Being subjected to elective surgery,
  • To be operated between 01 March 2021 and 31 December 2023.

Exclusion criteria

  • Patients requiring emergency surgery, patients requiring rapid serial intubation,
  • Patients who have already been taken to the operating room by intubation or tracheostomy,
  • Patients who will not be processed under general anesthesia,
  • Patients who do not have family consent and informed consent cannot be obtained

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

50 participants in 2 patient groups

Intubation with Flexible fiberoptic bronchoscopy
Active Comparator group
Description:
Patients were intubated with FFB and intubation success, intubation time, glottic visualization time and complications were recorded. FFB is considered the gold standard for airway management in both adult and pediatric patients with known or anticipated difficult airways.
Treatment:
Device: Flexible fiberoptic bronchoscopy
Intubation with Glidescope
Active Comparator group
Description:
Patients were intubated with Glidescope and intubation success, intubation time, glottic visualization time and complications were recorded. New generation videolaryngoscopy systems have also been successfully used as an alternative to FFB in pediatric patients with anticipated difficult airways. One of the most frequently used is Glidescope.
Treatment:
Device: Glidescope

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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