Airway Management Practice Patterns in Paediatric Anaesthesia: A Survey (SUR-AMPA)

June 22, 2016 updated by: Thekla Niebel, MD PhD, IRCCS Policlinico S. Matteo

A Survey of Airway Management Practice Patterns in Paediatric Anaesthesia by Anaesthesiologists in Different European Hospitals

Respiratory adverse events continue to be the leading reason for perioperative critical events in children. It is crucial for the anaesthesiologist to anticipate, recognize and treat these respiratory adverse events. Respiratory adverse events are one of the major causes of morbidity and mortality during paediatric anaesthesia. To avoid trouble, one must be prepared for trouble: if a difficult airway is very likely, anaesthesia should be administered by experienced anaesthesiologists and should only be performed in a protected well-equipped area where the personnel adequately trained.

This survey focuses on assessment and management of paediatric airway and highlights the unique challenges encountered in children.

Study Overview

Detailed Description

Airway management is one of the key areas of paediatric anaesthesia practice. The paediatric patients have significant anatomical and physiological differences compared with adults, which impact on the techniques and tools that the anaesthesiologist might choose to provide safe and effective control of the airway. Furthermore, there are a number of pathological processes, typically seen in the paediatric population, which present unique anatomical or functional difficulties in airway management. The presence of one of these syndromes or conditions can predict a "difficult airway".

Respiratory adverse events continue to be the leading reason for perioperative critical events in children. New developments in airway management in paediatric patients can only improve perioperative outcome if anaesthesiologists who are fully acquainted with these fundamental aspects of paediatric anaesthesia care for these children.

This survey was taken out within members of the Community of European Anaesthesiologists, to describe and explore current patterns of their airway management in paediatric anaesthesia.

The purpose of the study was to see whether there are more uniform practice patterns among anaesthesiologist with paediatric experience than those without paediatric experience.

Secondarily, the survey also explored anaesthetists'' knowledge about the risks of respiratory adverse events and, and about national organizations' recommendations.

Therefore, this survey highlighted some of the important anatomical and physiological differences and their implication in daily anaesthesiological practice.

Study Type

Observational

Enrollment (Anticipated)

200

Contacts and Locations

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

Study Contact

Study Locations

      • Pavia, Italy, 27100
        • Recruiting
        • IRCCS Policlinico San Matteo
        • Contact:

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Volunteers among the anaesthesiological community of 5 different European countries. All participant voluntarily response all items in the questionnaire database.

A representative anaesthesiologist for each of the target Countries will be asked to participate and to invite at least one other hospital. All anaesthesiologists within each selected hospital will be asked to participate in the survey.

Description

Inclusion Criteria:

  • Anaesthesiologists currently working in the operating rooms.

Exclusion Criteria:

  • unwilling to join the study

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

  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Expert
Anaesthesiologist with large paediatric daily practice. All participant voluntarily response all items in the questionnaire database.

The study type is a cross-sectional study, by means of electronic self-administered survey as online questionnaire sent by e-mail.

The questionnaire for the survey was developed with reference to previously published guidelines on the design of questionnaire surveys. The content validity of the questionnaire was verified by review of clinicians not participating into the project and by a statistician.

Non-experts
Anaesthesiologist with little paediatric daily practice. All participant voluntarily response all items in the questionnaire database.

The study type is a cross-sectional study, by means of electronic self-administered survey as online questionnaire sent by e-mail.

The questionnaire for the survey was developed with reference to previously published guidelines on the design of questionnaire surveys. The content validity of the questionnaire was verified by review of clinicians not participating into the project and by a statistician.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of anaesthesiologist with paediatric experience using intravenous induction compared to those without paediatric experience.
Time Frame: A time of survey; generally less than 20 minutes
The primary objective will be to compare anaesthesiologists with and without paediatric experience in terms of proportion of anaesthesiologists adopting "standard" practice.
A time of survey; generally less than 20 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Proportion of anaesthesiologist with paediatric experience measuring cuff pressure with pressure manometer compared to those without paediatric experience.
Time Frame: A time of survey; generally less than 20 minutes
The objective will be to compare anaesthesiologists with and without paediatric experience in terms of proportion of anaesthesiologists adopting "standard" practice.
A time of survey; generally less than 20 minutes
Proportion of participants correctly identifying predictability of difficult airway in children.
Time Frame: A time of survey; generally less than 20 minutes
To assess variables associated to adoption of standard practice, in particular: knowledge of the anatomical, physiological, and pathological features related to the airway.
A time of survey; generally less than 20 minutes
Proportion of participants correctly answering questions about the use of (modified) rapid sequence induction in the paediatric population.
Time Frame: A time of survey; generally less than 20 minutes
To compare anaesthesiologists with and without paediatric experience in terms of different practice patterns, and items explored by the questionnaire.
A time of survey; generally less than 20 minutes
Proportion of anaesthesiologist correctly identifying national organisations difficult airway recommendations.
Time Frame: A time of survey; generally less than 20 minutes
To informally compare practiced elicited within this study to existing guidelines and algorithms in paediatric anaesthesia.
A time of survey; generally less than 20 minutes

Collaborators and Investigators

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

Investigators

  • Study Chair: Antonio Braschi, MD Prof, IRCCS Policlinico San Matteo

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.

General Publications

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

January 1, 2016

Primary Completion (Anticipated)

January 1, 2017

Study Completion (Anticipated)

March 1, 2017

Study Registration Dates

First Submitted

June 14, 2016

First Submitted That Met QC Criteria

June 21, 2016

First Posted (Estimate)

June 22, 2016

Study Record Updates

Last Update Posted (Estimate)

June 23, 2016

Last Update Submitted That Met QC Criteria

June 22, 2016

Last Verified

June 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • AR-01-SUR-AMPA

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

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.

Clinical Trials on Paediatric Airway Management

Clinical Trials on Voluntarily response all items in the questionnaire.

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