Defining the 'Sniffing Position" in Infants and Toddlers - A Pilot Study

Sponsor
Tufts Medical Center (Other)
Overall Status
Completed
CT.gov ID
NCT04410289
Collaborator
(none)
40
1
2
5.8
6.8

Study Details

Study Description

Brief Summary

The "sniffing position" is widely accepted as a favorable position for direct laryngoscopy (DL) in both pediatric and adult patients. External anatomical markers are well documented to confirm proper 'sniffing position' in adults, but data on their use in the pediatric population is sparse. The investigators propose to define these markers in young children and investigate whether patients positioned using this standardized approach have better intubating conditions than those positioned randomly per the preference of the anesthesiologist.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Airway positioning per specified protocol followed by Direct Laryngoscopy and Endotracheal Intubation
  • Procedure: Airway positioning per provider preference followed by Direct Laryngoscopy and Endotracheal Intubation
N/A

Detailed Description

The procedure of endotracheal intubation in adults and children is a continuum, and begins with proper head positioning prior to direct laryngoscopy (DL). It is an accepted paradigm that proper positioning optimizes intubating conditions, and decreases subsequent airway maneuvers and manipulation.

The sniffing position is an accepted airway positioning concept in pediatric airway management, and continues to be recommended by experts and textbooks in the field. Anatomical peculiarities such as the large head relative to the torso in infants and toddlers is assumed to put the head in proper position when gently extended. However, reproducible parameters to confirm optimal head positioning remain vague and unclear. In the absence of objective and measurable markers, practitioners position infants and toddlers according to their individual preferences, and as such the procedure lacks definition and objective clarity.

The investigators plan to recruit 40 healthy patients between the ages of 1 month - 48 months and randomize them to be positioned either according to a predetermined algorithm or positioned freely according to the provider's preference. Patients randomized to the intervention group will be positioned with the aim to horizontally align the external auditory meatus (EAM) with the sternal notch (SN).

In summary, the study aims to define the sniffing position for infants and toddlers using reproducible objective secondary markers, and investigate whether a systematic approach to positioning using such markers improves direct laryngoscopic outcomes in the young pediatric patient population.

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
A Prospective Randomized Pilot Study to Define and Validate the Standard 'Sniffing Position' in Infants and Toddlers.
Actual Study Start Date :
Jul 1, 2019
Actual Primary Completion Date :
Nov 30, 2019
Actual Study Completion Date :
Dec 26, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

After induction of general anesthesia, and prior to direct laryngoscopy, patients in the intervention group were positioned using props horizontally aligning the external auditory meatus (EAM) with the sternal notch (SN) and the chin with the sinciput. A lateral side-profile photograph was taken for latter analysis and an Intubation Difficulty Scale (IDS) score card completed.

Procedure: Airway positioning per specified protocol followed by Direct Laryngoscopy and Endotracheal Intubation
Positioning of the patient's head and neck for the purpose of direct laryngoscopy and endotracheal intubation

Active Comparator: Control Group

After induction of general anesthesia, and prior to direct laryngoscopy, patients in the control group were positioned freely according to the provider's preference. A lateral side-profile photograph was taken for latter analysis and an Intubation Difficulty Scale (IDS) score card completed.

Procedure: Airway positioning per provider preference followed by Direct Laryngoscopy and Endotracheal Intubation
Positioning of the patient's head and neck for the purpose of direct laryngoscopy and endotracheal intubation

Outcome Measures

Primary Outcome Measures

  1. Difference in Intubation Difficulty Scale (IDS) Score [The brief time involved (5-10 minutes) involving the process of head positioning, direct laryngoscopy and endotracheal intubation.]

    To assess the difference in IDS scores between the study and control groups

Secondary Outcome Measures

  1. Angles of Deviation of the EAM-SN plane and Chin-Sinciput Plane from the Horizontal [Post-hoc analysis using a computer program to calculate angles. 10 minutes per patient.]

    Secondary outcome was to analyze and compare the degree of alignment or nonalignment of the EAM-SN plane and the sinciput-chin plane in both groups. Angles of deviation of the EAM-SN and chin-sinciput plane were measured in each cohort based on photographic data collected. A positive angle deviation indicated head flexion and a negative angle indicated head extension.

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Month to 48 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • healthy infants and toddlers undergoing non-emergent surgery under general anesthesia with an oral endotracheal tube
Exclusion Criteria:
  • neonates (infants under 1 month of age), infants and toddlers with congenital syndromes affecting the airway, and patients undergoing emergency surgery.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tufts Medical Center Boston Massachusetts United States 02111

Sponsors and Collaborators

  • Tufts Medical Center

Investigators

  • Principal Investigator: Aman Kalra, MD, Tufts Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Tufts Medical Center
ClinicalTrials.gov Identifier:
NCT04410289
Other Study ID Numbers:
  • 13188
First Posted:
Jun 1, 2020
Last Update Posted:
Jun 4, 2020
Last Verified:
Jun 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Tufts Medical Center

Study Results

No Results Posted as of Jun 4, 2020