How Easy is it to Identify the Cricothyroid Membrane in Children? Can Ultrasound Imagine be Used to Aid Identification?

How Easy is it to Identify the Cricothyroid Membrane in Children? Can Ultrasound Imaging me Used to Aid Identification?

The Investigators aim to determine how easy it is for anaesthetists to identify the Cricothyroid membrane (CTM) in children and infants and whether ultrasound maybe useful in addition. The investigators aim to conduct a randomised single blinded trial to compare methods to detect the CTM.

The first group of patients will be randomised to palpation of anatomical landmarks group. Prior to commencing the MRI scan the anaesthetist is timed to identify the CTM and then the trachea using a felt tip pen. A ficidual marker will be placed on the 2 marked areas.

The second group of patients will be randomised to receive ultrasound. Prior to commencing the MRI scan the sonographer is timed to identify the CTM and then the trachea using a felt tip pen. A ficidual marker will be placed on the two marked areas.

Study Overview

Status

Completed

Conditions

Detailed Description

Cricothyroidotomy is an infrequent but potentially life-saving procedure. The need for cricothyroidotomy arises from the can't intubate and can't ventilate (CICV) scenario and is therefore incorporated in the difficult airway guidelines for both adults and children. This CICV scenario is less common in the paediatric population than in the adult population and most difficult airways can be managed with-bag mask ventilation and PEEP.

The cricothyroid membrane is a useful place to access the airway in the case of glottic or supraglottic obstruction as it is relatively avascular, superficial and the 'full ring' of the cricoid protects against posterior perforation. In adults, the average the cricothyroid membrane CTM is 13.7mm long and 12.4mm wide. The CTM is relatively short in children. In neonates the CTM has a mean height of 2.6mm and a width of 3mm.

In children the most prominent anterior midline structures in the neck are not the thyroid as in adults but the hyoid bone and cricoid cartilage. As the larynx is more cephalad in children the cricothyroid membrane is higher than in adults and placement of a catheter may be more difficult as the mandible gets in the way. A healthy amount of adipose in the subcutaneous tissue can obscure the anatomy. Currently clinicians identify the CTM using palpation of anatomical landmarks. In infants, with the head in extension and soft tissue pulled up towards the mandible, the CTM may be difficult to distinguish. It is suggested that bimanual manipulation may enable identification of the cartilaginous trachea.

To perform a cricothyroid puncture, a syringe containing sterile saline is attached to a cannula. The skin over the cricothyroid membrane is stabilised with the index finger and thumb of the non-dominant hand. The transtracheal cannula is inserted through the cricothyroid membrane at a 45º angle heading caudal and posterior. However, in neonates due to the restricted dimensions, a needle is the only option for cricothyroidotomy. Even in experienced hands, cricothyroidotomy is technically challenging. In inexperienced hands this can lead to significant injuries including the risk of fracture of the thyroid and cricoid cartilages.

A recent abstract has tried to determine whether how easy it is to locate the CTM in children. Their initial conclusions suggest that the identification of the CTM is difficult. The limitations of their study are that there are small numbers and only one person has been asked to perform the identification.

The applications of ultrasound are vast and varied. It is readily available, portable and easy to use. Of note, a recent study has used ultrasound (Sonosite 10Hz) to help identify the CTM in adults. Following a period of training, it was found to improve accuracy and speed of identification.

The investigators aim to determine how easy it is for anaesthetists to identify the CTM in children and infants and whether ultrasound maybe a useful adjunct. The investigators aim to conduct a randomized single blinded trial to compare methods to detect the CTM: palpation of anatomical landmarks versus ultrasound .

Study Type

Interventional

Enrollment (Actual)

22

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • London, United Kingdom, WC1N 3JH
        • Great Ormond Street Hospital for Sick Children NHS Foundation Trust

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 6 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • All children between 0-8 years requiring general anaethesia for elective MRI head, neck and spinal scans

Exclusion Criteria:

  • Children with obvious neck deformity, goitre, tracheostomy and emergency cases

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: palpation
Group A: Palpation Group
Experimental: ultrasound
Group B: Ultrasound Group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Accuracy of placement of the marker
Time Frame: 4-6 months
Accuracy of the placement of the marker in relation to the cricithyroid membrane and trachea on MRI images.
4-6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time taken to identify CTM/Trachea
Time Frame: 4-6 months
Time taken to identify CTM/Trachea placement confidence assessed using the VAS Score (0-100: impossible to very confident). Comparison between age groups 0-4 years Vs 4-8 years.
4-6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nadine Dobby, MBBS, Great Ormond Street Hospital for Sick Children NHS Foundation Trust

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2011

Primary Completion (Actual)

November 1, 2012

Study Completion (Actual)

February 1, 2013

Study Registration Dates

First Submitted

June 1, 2012

First Submitted That Met QC Criteria

July 10, 2012

First Posted (Estimate)

July 11, 2012

Study Record Updates

Last Update Posted (Actual)

October 4, 2022

Last Update Submitted That Met QC Criteria

October 3, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 10AR11

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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