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

Acute Respiratory Failure Requiring Reintubation Clinical Trial

— ECHOLPE  

Official title:

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

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01857674
• Other study ID #: 2013-A00141-44
• Status: Recruiting
• Phase: N/A
• First received: May 16, 2013
• Last updated: August 1, 2013
• Start date: May 2013
• Est. completion date: December 2014

Study information

• Verified date: May 2013
• Source: Centre Hospitalier Universitaire de Besancon
• Contact: GINET MARC, MD
• Phone: 003338168289
• Email: mginet[@]chu-besancon.fr
• Is FDA regulated: No
• Health authority: France: The Commission nationale de l’informatique et des libertés
• Study type: Observational

Clinical Trial Summary

• 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 1000
• Est. completion date: December 2014
• Est. primary completion date: November 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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 Design

Time Perspective: Prospective

Related Conditions & MeSH terms

• Acute Respiratory Failure Requiring Reintubation
• Edema
• Laryngeal Edema
• Respiratory Distress Syndrome, Adult
• Respiratory Insufficiency

Locations

Country	Name	City	State
France	Centre Hospitalier Universitaire Besançon	Besançon

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire de Besancon

Country where clinical trial is conducted

France, 

References & Publications (4)

Ding LW, Wang HC, Wu HD, Chang CJ, Yang PC. Laryngeal ultrasound: a useful method in predicting post-extubation stridor. A pilot study. Eur Respir J. 2006 Feb;27(2):384-9. — View Citation

Frutos-Vivar F, Esteban A, Apezteguia C, González M, Arabi Y, Restrepo MI, Gordo F, Santos C, Alhashemi JA, Pérez F, Peñuelas O, Anzueto A. Outcome of reintubated patients after scheduled extubation. J Crit Care. 2011 Oct;26(5):502-9. doi: 10.1016/j.jcrc.2010.12.015. Epub 2011 Mar 3. — View Citation

Sustic A. Role of ultrasound in the airway management of critically ill patients. Crit Care Med. 2007 May;35(5 Suppl):S173-7. Review. — View Citation

Wittekamp BH, van Mook WN, Tjan DH, Zwaveling JH, Bergmans DC. Clinical review: post-extubation laryngeal edema and extubation failure in critically ill adult patients. Crit Care. 2009;13(6):233. doi: 10.1186/cc8142. Epub 2009 Dec 1. Review. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Performance of laryngeal ultrasonography in predicting major post extubation laryngeal edema in intensive care patients.	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	No
Secondary	Performance of laryngeal ultrasonography in predicting post-extubation stridor in intensive care patients.	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	No
Secondary	Frequency of major post-extubation laryngeal edema and post-extubation stridor	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	No
Secondary	Risk factors of major post-extubation laryngeal edema in intensive care unit	Several studies have identified risk factor for post-extubation laryngeal edema, but controversy remains.	From ICU admission to day of inclusion	No
Secondary	Evolution of ultrasonic parameters with corticotherapy 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	No
Secondary	Evaluation of impact of major post-extubation laryngeal edema occurence on mechanical ventilation duration, hospitalization duration and mortality in intensive care unit	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	No
Secondary	Inter-observer reproductibility of ultrasound scanning and ultrasonic air-leak volume measurement	In first 100 included patients,we would perform 2 laryngeal ultrasonograpy to assess inter-observer reproductibility of this new test.	Day 1 of inclusion	No