The Voice Analysis as a Preoperative Prediction Method of a Difficult Airway

September 27, 2023 updated by: Institut Universitari Dexeus

Before an anesthetic procedure, airway management is essential to ensure adequate ventilation and breathing of the patient during the entire surgical process.

The preanesthetic evaluation of the airway allows for proper planning, facilitates the anticipation of human resources and necessary means to face the possible challenges in a safe and efficient way. Orofacial mask ventilation and endotracheal intubation are a crucial step in general anesthesia. Most of the time, management is not complicated, but when an unpredicted difficult airway occurs, it is currently one of the most important challenges to face as an anesthesiologist. These situations are rare as the prevalence of a difficult airway is approximately 2.2% of the general population.

When there is a case of a difficult airway and adequate management is not achieved, very serious complications may occur including brain damage, cardio-respiratory arrest, aspiration of gastric content, traumatic airway injuries, tooth damage, unnecessary surgical access to keep the airway permeable or death. For these reasons, in anesthesia, an unforeseen difficult airway is considered a crisis situation. Therefore, a preoperative airway assessment is paramount.

Traditional predictive tests evaluate multiple anthropometric characteristics in which the physical presence of the patient is mandatory. However, no test can currently predict a difficult airway based on a single characteristic nor in the patient's absence. Nowadays, the optimization of resources and new technologies have increased interest in developing new tests or methods for preoperatively assessing the difficulty of the airway and new methods of airway evaluation have been proposed. As recently demonstrated, the detection of a difficult airway depends not only on the morphology but also on functional traits of the airway. Some studies propose the analysis of voice parameters as a reflection of anatomical and functional features of the superior airway.

The investigators propose that the analysis of voice characteristics could reflect the airway's anatomy and therefore the investigators will be able to predict a difficult airway, and this would enable the development of a voice-based assessment method which could have an promising role in facilitating telematic airway evaluation.

Study Overview

Status

Completed

Detailed Description

Proper airway management is essential for safe anesthesia practice. In particular, ventilation with an orofacial mask and endotracheal intubation are a crucial step in general anesthesia. The prevalence of a difficult airway is approximately 2.2% although it can vary greatly according to different groups of patients. It is defined, according to the American Society of Anesthesiology, as the clinical situation in which an experienced anesthesiologist has difficulty with ventilation using a face mask, during endotracheal intubation or both. Although other definitions also exist and include difficulty in ventilation or placement of supraglottic devices, difficult laryngoscopy defined by a 3 or 4 grade on the Cormack-Lehane scale or multiple attempts at intubation. A case of an unexpected difficult airway can lead to minor complications, such as loss or damage to teeth, pharynx or entail severe injuries, such as aspiration of gastric content, laryngeal lesions, respiratory failure, cardiorespiratory arrest or even death. Furthermore, complications increase considerably when there are no alternative plans and multiple repeated attempts at intubation are made.

Thus, the factors that mostly contribute to complications when an unanticipated difficult airway is found are due to deficiencies in identification, communication, preoperative planning and lack of training. An unpredicted difficult airway is a situation in which decision making is difficult, management is complex, and it is considered a crisis situation.

The importance of evaluation and management of the airway is such that different study groups within the main scientific societies of anesthesiologists are dedicated to studying and implementing protocols with the aim of avoiding these risky situations. A difficult airway should be detected during the pre-anesthetic visit, thus allowing the anesthesiologist to evaluate the patient, identify risk factors, advance to possible complications, and prepare an appropriate anesthetic plan. This means organizing both material and personal help, informing the patient; changing the type of anesthesia or even postponing elective surgeries to schedule them when the patient is correctly optimized making sure that the means in which the surgical procedure is safe.

Regardless of the surgical procedure and the initial anesthetic plan, the evaluation of the airway should always be performed with all patients since any sedation or regional anesthesia can be converted into a general anesthesia and require control of the airway.

In recent years, an increase in the efficiency of health procedures without the loss of safety or quality is expected. An attempt to protocolize a remote preoperative evaluation (telephone call) has been made which patients undergoing low complexity procedures. However, the most important limiting factor in remote pre-anesthetic evaluation is the inability to perform the airway assessment properly. Although there are risk factors that can be detected with a medical history such as a previous record of a difficult airway, obstructive sleep apnea syndrome, hoarseness, dysphonia or obesity, the traditional evaluative predictive tests require the physical presence of the patient and are based on the physical examination of the patient such as thyroid-chin distance, cervical mobility, mouth opening and subluxation capacity, or the assessment of pharyngeal structures by the Mallampati test consisting of the direct visualization of the upper airway. However, no test can predict a difficult airway based on a single characteristic in the patient's absence.

The combined evaluation of several risk factors obtains greater sensitivity than when analyzed in isolation. This is the case of the Arné Test, which consists of a multifactorial index that offers a sensitivity and specificity greater than 90% to predict a difficult airway when a score greater than or equal to 11 is obtained. In this context, new evaluation methods have appeared, such as ultrasound or other imaging tests, which intend to correlate the anatomical images of the airway with the presence of a difficult airway. But, the detection of a difficult airway depends not only on the morphology, but also on its functional characteristics. With the introduction of new technologies many attempts to develop other methods to predict a difficult airway such as facial recognition based on image processing have been made, however they have not succeeded yet. Other investigators propose the analysis of voice parameters as a reflection of anatomical and functional characteristics of the superior airway. Specifically, studies carried out in the field of maxillofacial surgery describe how the expansion of the maxilla affects the widening of the upper airway and, consequently, in the formation of the vowels and how this translates into a variation in the properties of the voice, such as frequency or amplitude. Accordingly, the investigators propose that voice characteristic analysis could reflect the airway's anatomy and be able to predict a difficult airway.

Building on this, the investigators aim to develop a voice airway assessment method that replaces anthropometric parameters evaluated in traditional tests to predict a difficult airway, facilitating a remote airway evaluation.

Voice recording will be made through a smart phone application to patients who are going to undergo general anesthesia and require orotracheal or nasotracheal intubation, by direct laryngoscopy, at the pre-anesthetic visit. The day of the surgical procedure, the result of the intubation - whether or not a difficult airway exists- will be registered.

The records of the mobile application database will be downloaded, the voice signal will be processed, and parameters related to frequency, morphology and perturbation will be extracted employing Matlab® as these are considered continuous variables, to determine the statistical significance of the differences within parameters. The non-parametric test of Kolmogorov-Smirnov will be used for an easy and a difficult independent airway groups. Thus, these variables will be introduced into several classification algorithms obtained by combined methods using machine learning in order to predict the classification of patients according to the Cormack scale grade and sensitivity and specificity will be determined to assess their ability to predict a difficult airway. The area under the receiver operating characteristic curve will be used to assess the ability of the method to predict difficulty.

The recruitment period will take place over a period of 12 months or until the estimated sample size is reached. The total duration of the study will be approximately 6 months years, ending with a total of 800 patients.

Study Type

Observational

Enrollment (Actual)

722

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 Contact Backup

Study Locations

      • Barcelona, Spain, 08028
        • Hospital Universitario Dexeus

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 and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Patients who will undergo general anesthesia by orotracheal or nasotracheal intubation

Description

Inclusion Criteria:

  • American Society of Anesthesiologists classification I-III
  • Adults over 18 years
  • Scheduled for intervention or surgical procedure in need of orotracheal or nasotracheal intubation by direct laryngoscopy
  • Patients who have given their informed consent

Exclusion Criteria:

  • American Society of Anesthesiologists classification > III
  • Minors
  • Emergency procedures
  • Patients who refuse to participate in 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difficult Airway Criteria (through Arne Test)
Time Frame: Baseline
Arne Test assessment evaluates different parameters giving a punctuation depending on the selected level. If the total score is higher than 11 points, the airway is predicted to be a difficult tracheal intubation. Parameters of the scale: Distance between incisors (> 5cm, 3.5-5cm, ≤ 3.5cm), Mandibular subluxation (Normal, moderate restriction, severe restriction), Thyromental distance (> 6.5cm ≤ 6.5cm), Neck movement range (> 100º, 90º, <80º), Mallampati (I, II, III, IV), Total Arné Test score (if greater than 11, considered difficult airway).
Baseline
Voice power spectrum
Time Frame: Baseline

Power description of the different vocals within the voice record of the patient.

Power is calculated using the spectrogram that uses the Fourier transformation. Spectrogram shows the power in decibel of the signal within a time-window and through different frequency intervals.

Baseline
Voice pitch frequency
Time Frame: Baseline

Pitch frequency is defined as the number of oscillations of the vocal cords per second.

Calculation is made using the glottic pulses. Pitch frequency is the mean of all the pulses from the analysed signal.

Baseline
Voice formants
Time Frame: Baseline
Formants constitute the transference function of the vocal tract. Voice formant are a group of frequencies characterized by its central frequency, bandwidth and energy. They are extracted from the Fourier Transform.
Baseline
Voice harmonics
Time Frame: Baseline
Parameters that depend on the pronounced vocal and the vocal tract morphology. Vocal harmonics are the resonances produced by the vocal tract. They are calculated detecting the peaks of the Fourier Transformation.
Baseline
Jitter measurements
Time Frame: Baseline
Jitter measures the increase of perturbations of the voice frequency cycle per cycle. There are four variants, depending on the number of analysed cycles.
Baseline
Shimmer measurements
Time Frame: Baseline
Shimmer measures the increase of perturbations of the voice amplitude cycle per cycle. There are four variants, depending on the number of analysed cycles.
Baseline
Harmonic to noise ratio
Time Frame: Baseline
Harmonic to noise ratio is the relation of the energy of harmonics compared to the energy considered noise. It is a parameter to determine the voice purity.
Baseline
Voice Turbulence Index
Time Frame: Baseline
Voice turbulence index measures the relation of the high-frequency energy (2.5kHz-5.8kHz) to the low-frequency energy (50Hz-2.5kHz) within the voice signal.
Baseline
Normalized Noise Energy
Time Frame: Baseline
Normalized Noise energy measures the noise in the voice signal caused by incomplete closure of the glottis due to the presence of pathologies in the phonation apparatus. It is the relation between the noise power and the total signal power .
Baseline
Intubation process
Time Frame: Baseline

To analyse the intubation process the next categorical variables are collected:

Cormack-Lehane scale grade (I, II, III, IV) that determines the visible structures of the larynx when direct intubation.

Type of maneuver (single, repeated or imposible) to determine the number of times intubation is performed.

Device used to determine if the intubation is performed through direct laryngoscopy or a device has been used.

Baseline

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Claudia Rodiera, M.D., Institut Universitari Dexeus

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)

March 1, 2020

Primary Completion (Actual)

September 1, 2022

Study Completion (Actual)

September 1, 2022

Study Registration Dates

First Submitted

December 17, 2019

First Submitted That Met QC Criteria

February 5, 2020

First Posted (Actual)

February 6, 2020

Study Record Updates

Last Update Posted (Actual)

September 28, 2023

Last Update Submitted That Met QC Criteria

September 27, 2023

Last Verified

September 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • DEX-ANE-2019-001

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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