Airway Ultrasonography Measurements With Cormack Lehane Classification in Patients With OSA

February 23, 2021 updated by: Rhendra Hardy Mohamad Zaini, Universiti Sains Malaysia

The Correlations of the Findings Obtained From Airway Ultrasonography With Cormack Lehane Classification in Patients With Obstructive Sleep Apnoea - A Cross Sectional Study

Airway assessment using ultrasonography can provide an additional information in identifying difficult intubation in OSA patients. The main purpose of this study is to find the correlation of the ultrasound parameters and the Cormack Lehane Score (CL Score) as well as to identify the cut-off point of the ultrasound parameters that would differentiate between the easy and difficult intubation.

Study Overview

Status

Completed

Detailed Description

Research design

  1. This is a cross sectional study. Involving face-to-face interview, USG airway assessment and Cormack Lehane score assessment. The patient will be identified from locations listed below:

    • Anaesthesia clinic
    • In the ward, during review by anaesthesia team for elective operation in the following day
    • In the ward, when cases are notified for operations as emergency case
  2. Once consent obtained from the patient, information regarding surgery and date of surgery will be recorded in the patient's data collection sheet. Patient's STOPBANG score and AHI score will also be recorded.
  3. The airway ultrasonography will be performed by the principal investigator using a standardized ultrasound machine (NextGen LOGIC e Ultrasound with 12L-RS wide band linear array 5-13 MHz frequency probe) under supervision by a radiologist. The procedure will be performed at the recovery bay in the operation theatre. The following measurements will be done and recorded for future statistical analysis.

    • Depth of preepiglottic space (PE)
    • Distances between epiglottis and midpoint between 2 vocal cords (E-VC)
  4. Cormack Lehane score will be obtained during induction of General Anaesthesia and Intubation in OT on the specified OT date. Conventional direct laryngoscope will be used for CL score determination. Medical Officer of more than 2 years' experiences in anaesthesiology will be requested to intubate the patient to minimize bias. CL scores are as described below

CL 1: Most of glottis Visible CL 2: Half of the glottis seen CL 3: Only epiglottis visible CL4: No laryngeal structure visible

Study area: Hospital Sultanah Nurzahirah, Kuala Terengganu Study population: Adult patient age between 18 to 65, diagnosed or suspected OSA, planned for operation under General Anaesthesia

Sample size estimation

  1. st Objective :

    • To determine the correlation between airway ultrasonography measurements and CL score.
    • Using R package pwr

      • For PE

        • r: 0.595 (based on Gupta D, 2012), significant level 0.05, power: 0.8
        • Number of sample: 19
      • For E-VC

        • r: -0.966 (based on Gupta D,2012), significant level 0.05, power: 0.8)
        • Number of sample: 4
      • For ratio PE/E-VC

        • r: 0.495 (based on Gupta D, 2012), significant level 0.05, power: 0.8)
        • Number of sample: 28
  2. nd and 3rdobjective

    • 2nd objective: To determine the best cut off point of airway ultrasonography measurement in predicting the difficulty in intubation using CL (difficult vs less difficult)
    • 3rd objective: To determine the accuracy of cut-off point in determining difficult intubation. (AUC) )
    • Receiver Operating characteristics (ROC) curve power calculation using R

      • Significance level: 0.05
      • Power of study: 0.8
      • Kappa: 4
      • AUC: 0.7

Based on previous study, the incidence of difficult intubation in OSA patient is 19.3%. Hence kappa: 4. Using pROC package in R, based on the above values and data, the investigators need at least 24 cases of difficult intubation and 41 cases of non-difficult intubation (to detect AUC of 0.7 from 0.5 null hypothesis). So, total patients required is at least 65

Sampling method and subject recruitment As mentioned above, this is a cross sectional study. Involving face-to-face interview, USG airway assessment and Cormack Lehane score assessment. After the samples identified at the specific locations mentioned and they will be approached for consent. Once agreed, the patient will be recruited for the study.

Data analysis

Statistical Analysis Plan For objective 1

• Intended statistical analysis: Spearman correlation

For objective 2 and 3

  • Using ROC curve
  • outcome: difficulty status (0 or 1)
  • test variable: PE, E-VC and ratio PE/E-VC

AUC in the ROC curve will be calculated accordingly based on the study results

Study Type

Observational

Enrollment (Actual)

71

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

    • Kelantan
      • Kubang Kerian, Kelantan, Malaysia, 16150
        • University of Science Malaysia Hospital

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Adult patient age between 18 to 65, diagnosed or suspected OSA, planned for operation under General Anaesthesia

Description

Inclusion Criteria:

  1. Age between 18-65
  2. Diagnose / screened OSA
  3. Planned for operation under General Anaesthesia
  4. American Society Of Anaesthesia (ASA) physical status class I-III

Exclusion Criteria:

  1. Unstable haemodynamic status
  2. Patient refusal to participate
  3. Altered mental status, cognitive function or mental disorder
  4. Distorted head and neck anatomy

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Correlation between airway ultrasonography measurements and CL score
Time Frame: may 2017-may 2018
ultrasound measurements
may 2017-may 2018
Cut off point of airway ultrasonography measurement in predicting the difficulty in intubation using CL
Time Frame: may 2017-may 2018
ultrasound measurements
may 2017-may 2018
Accuracy of each cut off point in objective 2
Time Frame: may 2017-may 2018
cut off point to differentiate between easy and difficult intubation
may 2017-may 2018

Collaborators and Investigators

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

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, 2017

Primary Completion (Actual)

May 1, 2018

Study Completion (Actual)

January 1, 2019

Study Registration Dates

First Submitted

March 30, 2019

First Submitted That Met QC Criteria

April 1, 2019

First Posted (Actual)

April 2, 2019

Study Record Updates

Last Update Posted (Actual)

February 26, 2021

Last Update Submitted That Met QC Criteria

February 23, 2021

Last Verified

February 1, 2021

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

Clinical Trials on Obstructive Sleep Apnea

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