Evaluation of Laryngeal Ultrasonography Performance in Predicting Major Post Extubation Laryngeal Edema in Intensive Care Patients (ECHOLPE)

  • For patient in intensive care unit, extubation failure is defined as the necessity of early reintubation after scheduled extubation, with Increased morbidity and mortality, so it seems important to quickly identify patients with high risk of post-extubation acute respiratory failure.
  • Major post-extubation laryngeal edema is one of extubation failure causes, and its incidence vary in literature from 4 to 37%.
  • We can't currently predict arising of a major post-extubation laryngeal edema. However, a recent pilot study showed that laryngeal ultrasonography could help to identify patients with high risk of post-extubation stridor, measuring ultrasonic leak volume and cuff-deflated air-column width, of which we propose to assess diagnostic performance.

Study Overview

Detailed Description

Definitions:

Intubation is a traumatism for laryngeal mucous membrane. Due to local inflammatory reaction, laryngeal edema occurs in nearly all intubated patients, but only some of them develop clinical symptoms, as post-extubation stridor or acute respiratory distress. Stridor is commonly defined as a high-pitched sound produced by airflow through a narrowed airway, and accepted as a clinical marker of post-extubation laryngeal edema. The main complication of post-extubation laryngeal edema is reintubation, defining major post-extubation laryngeal edema. Early recognition of laryngeal edema is essential since these patients have the highest risk of evolving to respiratory distress and extubation failure. Even before extubation, signs indicative of laryngeal edema may be present. The search for a test that adequately identifies patients at risk for extubation failure is ongoing.

Trial Procedures:

  • At day 0: Selection of patients filling inclusion criteria. Oral and written information of patient and his refer person, and collecting of non-opposition.
  • At day 0: inclusion of patients ventilated with inspiratory assistance just before schedulded extubation. Information of patient on procedure course.
  • First ultrasonography of protocol: The patient is in the supine position, with the neck hyper-extended, and the probe is placed on cricothyroid membrane with a transverse view of the larynx. The standard scanning plane is predetermined: it should contain several landmarks, including the vocal cords, false cords, thyroid cartilage and arytenoids cartilage. The oral and laryngeal secretions are suctioned. Ultrasonic air-leak volume is defined by difference between air-column width cuff inflated and air-column width cuff deflated. Shape of air-column cuff inflated and cuff deflated is also recorded in observation notebook.
  • Then the patient is extubated after spontaneous ventilation trial, according to unit protocol, by the physician in charge. After extubation, surveillance of post-extubation stridor and acute respiratory distress occurrence during the first 24 hours.
  • If the patient is reintubated for major post-extubation laryngeal edema, onset of 48 hours corticotherapy, and realization of second, third and fourth laryngeal ultrasonography, daily to next schedulded extubation.
  • At discharge of intensive care unit, data collection about mechanical ventilation duration, intensive care hospitalization duration, occurrence of ventilation-acquired pneumopathy, mortality at 28 days.

Study Type

Observational

Enrollment (Anticipated)

1000

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

      • Besançon, France, 25000
        • Recruiting
        • Centre Hospitalier Universitaire Besançon
        • Sub-Investigator:
          • Guillaume BESCH, MD
        • Contact:
        • Principal Investigator:
          • Marc GINET, MD
        • Sub-Investigator:
          • Sébastien PILI-FLOURY, MD, PhD
        • Sub-Investigator:
          • Emmanuel SAMAIN, MD, PhD
        • Sub-Investigator:
          • Gilles CAPELLIER, MD, PhD
        • Sub-Investigator:
          • Marion COLNOT, Interne

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

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All Adults were admitted to the surgical (20 beds) and medical (20 beds)intensive care unit of besançon University Hospital.

Description

Inclusion Criteria:

  • Adults
  • Intubated and ventilated for more than 48 hours.
  • Filling mechanical ventilation weaning criteria according to the 6th consensus conference on intensive care medicine.
  • Affiliated to French Sociale Sécurity.

Exclusion Criteria:

  • Pregnant or breast-feeding woman
  • Under 18 or under guardianship patients
  • Laryngeal pathology: benign or malignant tumor, unilateral or bilateral paralysis of recurrent laryngeal nerve, laryngitis
  • Past history of cervical surgery or radiotherapy
  • Technical impossibility of laryngeal ultrasonography: wound or locale infection in ultrasonic plan
  • Self-extubation or accidental extubation
  • Refusal to take part 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

  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Performance of laryngeal ultrasonography in predicting major post extubation laryngeal edema in intensive care patients.
Time Frame: Within the first 24 hours after extubation

Sensitivity, specificity, positive predictive value and negative predictive value of ultrasonic air-leak volume in predicting major post-extubation laryngeal edema in intensive care patients.

A post-extubation laryngeal edema is major when inducing acute respiratory failure requiring early reintubation.

We assume that, among patients with post-extubation laryngeal edema,the ultrasonic air-leak volume is lower than among patients without post-extubation laryngeal edema.

Within the first 24 hours after extubation

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Performance of laryngeal ultrasonography in predicting post-extubation stridor in intensive care patients.
Time Frame: Within the first 24 hours after extubation

Sensitivity, specificity, positive predictive value and negative predictive value of ultrasonic air-leak volume in predicting post-extubation stridor.

Post-extubation stridor is commonly defined as a high-pitched sound produced by airflow through a narrowed airway, and is accepted as a clinical marker of laryngeal edema following extubation. So stridor is widely used as outcome measure for post-extubation laryngeal edema.

Within the first 24 hours after extubation
Frequency of major post-extubation laryngeal edema and post-extubation stridor
Time Frame: Within the first 24 hours after extubation
In literature, incidence of post-extubation stridor is from 2 to 15%, and incidence of major post-extubation laryngeal edema is from 4 to 37%. We would confront incidence of post-extubation laryngeal edema in our cohort and in literature.
Within the first 24 hours after extubation
Risk factors of major post-extubation laryngeal edema in intensive care unit
Time Frame: From ICU admission to day of inclusion
Several studies have identified risk factor for post-extubation laryngeal edema, but controversy remains.
From ICU admission to day of inclusion
Evolution of ultrasonic parameters with corticotherapy after reintubation for a major post-extubation laryngeal edema
Time Frame: Daily from day 1 to day 3 after reintubation for a major post-extubation laryngeal edema
The recommended treatment of major post-extubation laryngeal edema is corticotherapy during 48 hours. By an anti-inflammatory effect, the swelling of laryngeal area decreases under corticoids, so we assume that there is a modification of ultrasonic parameters values during this period.
Daily from day 1 to day 3 after reintubation for a major post-extubation laryngeal edema
Evaluation of impact of major post-extubation laryngeal edema occurence on mechanical ventilation duration, hospitalization duration and mortality in intensive care unit
Time Frame: Within 28 days after inclusion in study
Occurence of major post-extubation laryngeal edema leads to increase morbidity and mortality because of reintubation and its complications. In our cohort, some patients would need to be reintubate, others don't, so we would confront data between these 2 groups.
Within 28 days after inclusion in study
Inter-observer reproductibility of ultrasound scanning and ultrasonic air-leak volume measurement
Time Frame: Day 1 of inclusion
In first 100 included patients,we would perform 2 laryngeal ultrasonograpy to assess inter-observer reproductibility of this new test.
Day 1 of inclusion

Collaborators and Investigators

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

Publications and helpful links

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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

May 1, 2013

Primary Completion (Anticipated)

November 1, 2014

Study Completion (Anticipated)

December 1, 2014

Study Registration Dates

First Submitted

May 16, 2013

First Submitted That Met QC Criteria

May 16, 2013

First Posted (Estimate)

May 20, 2013

Study Record Updates

Last Update Posted (Estimate)

August 2, 2013

Last Update Submitted That Met QC Criteria

August 1, 2013

Last Verified

May 1, 2013

More Information

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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