Evaluation of Laryngeal Ultrasonography Performance in Predicting Major Post Extubation Laryngeal Edema in Intensive Care Patients
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Laryngeal Edema
- Sponsor
- Centre Hospitalier Universitaire de Besancon
- Enrollment
- 1000
- Locations
- 1
- Primary Endpoint
- Performance of laryngeal ultrasonography in predicting major post extubation laryngeal edema in intensive care patients.
- Last Updated
- 12 years ago
Overview
Brief 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.
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.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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
Outcomes
Primary Outcomes
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.
Secondary Outcomes
- Performance of laryngeal ultrasonography in predicting post-extubation stridor in intensive care patients.(Within the first 24 hours after extubation)
- Frequency of major post-extubation laryngeal edema and post-extubation stridor(Within the first 24 hours after extubation)
- Risk factors of major post-extubation laryngeal edema in intensive care unit(From ICU admission to day of inclusion)
- Evolution of ultrasonic parameters with corticotherapy after reintubation for a major post-extubation laryngeal edema(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(Within 28 days after inclusion in study)
- Inter-observer reproductibility of ultrasound scanning and ultrasonic air-leak volume measurement(Day 1 of inclusion)