Emergency Front of the NecK Access (eFONA) in Children (eFONA)

January 10, 2019 updated by: University Hospital Inselspital, Berne

Pediatric Emergency Front of the Neck Access (eFONA): Assessing a Novel Experiential Learning Approach

Study participants will be shown an illustrated training video demonstrating and explaining the RST. The video may be reviewed until the participant feels confident to perform procedure.

The Rapid Sequence Tracheostomy (RST) consists of the following steps:

  1. Orientational palpation and vertical midline skin incision followed by separation of the strap muscles
  2. Exposure of the trachea and cricoid followed by anterior luxation of the trachea with a Backhaus towel clamp
  3. Perform a vertical puncture with a tip scissors between the Cricoid and 1st tracheal ring followed by a vertical incision of no more than 2 rings in length.
  4. An age adapted tracheal tube is inserted into the trachea and the lungs are ventilated.

Teaching methodology: Prior to the hands-on training of eFONA, all participants shall watch a 2-minute training video of RST performed on rabbit cadaver following the steps outlined above. During video demonstration, no additional explanation or support will be provided.

Once study participants express confidence to perform the skill, participants shall attempt to perform the RST 10 times. During the RST procedure no additional explanation or support will be provided. Study participants will be allowed to watch the video again between attempts, if needed. Each attempt will be video recorded and time recorded for rater analysis, as outlined above. Successful tracheotomy is defined as ventilation of the lungs by way of a standard self-inflating bag that is to be connected to the tracheal tube or visual confirmation of the tube being placed at least 2 cm inside the trachea (dissection of the rabbit cadaver performed by assistant).

Study Overview

Detailed Description

Current difficult airway algorithms end with the need for tracheal airway access to be obtained via Front Of Neck Access (FONA) to achieve oxygenation. In children < 8 years existing recommendations and the literature do not offer guidance on how to perform emergent FONA. Emergent tracheotomy is the potentially life-saving procedure - which needs to be performed without delay. When emergent tracheotomy is attempted in children < 8 years of age, there is a substantial risk for complications. As a result, health care providers who do not have routine at performing this procedure are often reluctant to perform FONA, Diameters, vertical/horizontal dimensions, vocal cord distance, larynx position, and cricothyroid membrane size of the rabbit airway suggest considerable similarities with infant airways, making it a good model to learn this technique. The FONA rapid sequence technique (RST) is a simple technique suitable for emergent pediatric tracheotomy. RST outlines 4 clearly defined steps, that enable airway establishment.

Step 1: Vertical midline skin incision and separate the strap muscles Step 2: Expose trachea and cricoid through palpation, lift and immobilize trachea with a clamp Step 3: Vertical trachea incision with the sharp tip scissors (2 cm) Step 4: Open the trachea and insert the tube The steps are easy to perform, if sufficiently practiced. Anesthesiologist, pediatric intensivists, surgeons, and emergency physicians who are most likely to need to perform FONA in small children, shall learn to perform RST emergent pediatric tracheotomy in less than 60 seconds. The investigators seek to measure and study learning curves of participants for establishing an artificial airway using the RST.

Hypothesis: After having practiced the procedure 10 times, 80% of study participants will not be able to successfully demonstrate FONA within 60 seconds. Alternative hypothesis: study participants will be able to successfully demonstrate FONA within 60 seconds.

Single-center interventional trial. The only inclusion criterion is informed consent. A high quality instructional video demonstrating the RST on a rabbit cadaver will teach the participants. Performance time will be defined (from touching the skin until ventilation of the trachea with a standard self-inflating bag connected to the tube). The investigators seek to assess the learning curves of participants.

Sample size. In order to obtain a lower limit of the 95% Confidence interval of 80% success in FONA the investigators would need 40 study participants assuming 2 failures by the 10th attempt. Statistical methods: Descriptive statistics for demographics. To establish the learning curve the increase over the 3 attempts will be analyzed by repeated ANOVA or Friedman.

For the reasons outlined above the investigators will provide a suitable and valid training model for pediatric airway practitioners to practice the invasive front of neck access technique.

Study Type

Interventional

Enrollment (Actual)

50

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

      • Bern, Switzerland, 3010
        • University Hospital Bern

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

25 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Inclusion criteria are informed consent, no previous experience in FONA.

Exclusion Criteria:

none

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: Non-Randomized
  • Interventional Model: Sequential Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Pediatric anesthesiologist
10 rapid sequence tracheostomy (RST) on rabbit cadaver

The Rapid Sequence Tracheostomy (RST) consists of the following steps:

  1. Orientational palpation and vertical midline skin incision followed by separation of the strap muscles
  2. Exposure of the trachea and cricoid followed by anterior luxation of the trachea with a Backhaus towel clamp
  3. Perform a vertical puncture with a tip scissors between the Cricoid and 1st tracheal ring followed by a vertical incision of no more than 2 rings in length.
  4. An age adapted tracheal tube is inserted into the trachea and the lungs are ventilated.
Experimental: Pediatric intensivists
10 rapid sequence tracheostomy (RST) on rabbit cadaver

The Rapid Sequence Tracheostomy (RST) consists of the following steps:

  1. Orientational palpation and vertical midline skin incision followed by separation of the strap muscles
  2. Exposure of the trachea and cricoid followed by anterior luxation of the trachea with a Backhaus towel clamp
  3. Perform a vertical puncture with a tip scissors between the Cricoid and 1st tracheal ring followed by a vertical incision of no more than 2 rings in length.
  4. An age adapted tracheal tube is inserted into the trachea and the lungs are ventilated.
Experimental: Pediatric surgeons
10 rapid sequence tracheostomy (RST) on rabbit cadaver

The Rapid Sequence Tracheostomy (RST) consists of the following steps:

  1. Orientational palpation and vertical midline skin incision followed by separation of the strap muscles
  2. Exposure of the trachea and cricoid followed by anterior luxation of the trachea with a Backhaus towel clamp
  3. Perform a vertical puncture with a tip scissors between the Cricoid and 1st tracheal ring followed by a vertical incision of no more than 2 rings in length.
  4. An age adapted tracheal tube is inserted into the trachea and the lungs are ventilated.
Experimental: Pediatric emergency physicians
10 rapid sequence tracheostomy (RST) on rabbit cadaver

The Rapid Sequence Tracheostomy (RST) consists of the following steps:

  1. Orientational palpation and vertical midline skin incision followed by separation of the strap muscles
  2. Exposure of the trachea and cricoid followed by anterior luxation of the trachea with a Backhaus towel clamp
  3. Perform a vertical puncture with a tip scissors between the Cricoid and 1st tracheal ring followed by a vertical incision of no more than 2 rings in length.
  4. An age adapted tracheal tube is inserted into the trachea and the lungs are ventilated.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Performance time
Time Frame: 60 seconds
The primary outcome will be performance time of RST representing the time from touching the skin until ventilation of the trachea (visualized by lung expansion) indicating the artificial airway as established. Performance time will yield learning curves. The declared intention is to perform RST in less than 60 seconds. Failed/aborted RST will be registered as a 5-minute attempt
60 seconds

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of attempts
Time Frame: 1 hour
Number of attempts to perform the skill in <60 s
1 hour
Number of attempts for plateau
Time Frame: 1 hour
Number of attempts to reach a time plateau
1 hour
Preparation of the trachea
Time Frame: 60 seconds
Time to vertical incision of the trachea with the sharp tip scissors
60 seconds
Vertical incision
Time Frame: 60 seconds
Time to vertical incision of the trachea with the sharp tip scissors
60 seconds
Training
Time Frame: 1 hour
Number of times that training video was watched
1 hour
Suitability
Time Frame: 1 hour
The subjective rating of the suitability of the given training model
1 hour

Collaborators and Investigators

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

Investigators

  • Study Chair: Greif Robert, Prof., Department Anesthesia and Pain Therapy, University Hospital Bern

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

May 1, 2018

Primary Completion (Actual)

November 10, 2018

Study Completion (Actual)

December 23, 2018

Study Registration Dates

First Submitted

June 18, 2018

First Submitted That Met QC Criteria

July 2, 2018

First Posted (Actual)

July 3, 2018

Study Record Updates

Last Update Posted (Actual)

January 11, 2019

Last Update Submitted That Met QC Criteria

January 10, 2019

Last Verified

January 1, 2019

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Riva-Ulmer2017

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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