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Acute respiratory distress syndrome remains a serious condition, with a mortality rate of between 30 and 50%. The use of mechanical ventilation with small tidal volumes, and by limiting the plateau pressure in the respiratory tract below 30 cm H2O has been shown to reduce mortality by approximately 10%, probably by reducing pulmonary hyperinflation and pulmonary lesions induced by mechanical ventilation. It is therefore now established that the respirator settings influence patient prognosis. However, around 30% of patients with ARDS ventilated with these settings supposedly protective continue to present signs of pulmonary hyperinflation on tomodensitometry, suggesting an additional reduction in the tidal volume could be required in certain patients. Electrical impedance tomography (EIT) is a new imaging technique that gathers functional pulmonary information at bedside.
This technique also allows a regional analysis, allowing the complexity of the spatial distribution of ARDS pulmonary lesions to be understood. The hypothesis is that EIT is a reliable method to detect at-risk situations of lesions induced by mechanical ventilation among patients with ARDS.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ventilatory conditions and measures with scanner and EIT | Experimental | The patient is installed on the scanner bed, EIT electrodes are connected to the acquisition device of the EIT signal. Esophageal pressure signals, pressure and flow in the airways will be acquired continuously |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ventilatory conditions and measures with scanner and EIT | Procedure | Different ventilatory conditions are studied and measures are acquired with scanner and EIT Time A: measure under basal conditions (TVbasal=6ml/kg of predicted weight), basal PEP, basal inspiratory time / total time = 30%) Time B: different PEP are applied for 4 minutes: 5, 10, 15, 20 cm of H2O conserving the basal TV Time C: different TV are applied for 4 minutes: 4, 7, 10 ml/kg of predicted weight conserving the basal PEP and the basal inspiratory time Time D: recruitment in continuous positive airway pressure at 45 cm of H2O is performed for 30 seconds Time E: return to adjustment period A |
| Measure | Description | Time Frame |
|---|---|---|
| mean values of optimal PEP obtained by EIT | Data acquisition will be carried out for 2 minutes and will start after 2 minutes of applying each ventilatory long time experience (A, B, C, E). mean values of optimal PEP will be compared between the 2 methods (scan and EIT). | after 2 minutes of applying each ventilatory experience |
| mean values of optimal TV obtained by EIT | Data acquisition will be carried out for 2 minutes and will start after 2 minutes of applying each ventilatory long time experience (A, B, C, E). mean values of optimal TV will be compared between the 2 methods (scan and EIT) | after 2 minutes of applying each ventilatory experience |
| mean values of optimal PEP obtained by scan | Data acquisition will start after 4 minutes of applying each ventilatory long time experience (A, B, C, D). mean values of optimal PEP will be compared between the 2 methods (scan and EIT). | after 4 minutes of applying each ventilatory experience |
| mean values of optimal TV obtained by scan | Data acquisition will start after 4 minutes of applying each ventilatory long time experience (A, B, C, D). mean values of optimal TV will be compared between the 2 methods (scan and EIT). | after 4 minutes of applying each ventilatory experience |
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Inclusion Criteria:
Exclusion Criteria:
Excessively serious respiration precluding the modifications to ventilation planned in the protocol
Contraindication for transport to the radiology department
Without reliable monitoring during transport of the patient to the radiology department
Intracranial hypertension
Impossible to apply EIT electrodes on the thorax of the patient (burns, dressings, …)
Undrained pneumothorax or bronchopleural fistula
Scanner unavailable for the study (broken down, overloaded program, …)
Contraindication esophageal balloon catheter
Patient previously included in the study
Vulnerable persons (as defined in laws L1121-5 to L1121-7, L1121-8 and L1122-1-2
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hôpital de la Croix Rousse | Lyon | France |
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|
| ID | Term |
|---|---|
| D012128 | Respiratory Distress Syndrome |
| ID | Term |
|---|---|
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D012120 | Respiration Disorders |
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| ID | Term |
|---|---|
| D014894 | Weights and Measures |
| ID | Term |
|---|---|
| D008919 | Investigative Techniques |
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