Determination of Normal Values of Regional Pulmonary Strain Using a New Ultrasonographic Tool in Healthy Volunteers
Mechanical Ventilation ComplicationMechanical ventilation is frequently used in the operating room and the intensive care settings. Although essential in many cases, mechanical ventilation can be responsible for ventilator-induced lung injury (VILI). The relationship between mechanical ventilation and VILI has been clearly demonstrated in animals and is highly suspected in humans. The putative mechanism responsible for VILI is excessive pulmonary strain or overdistension. Frequently observed in mechanically ventilated patients, the presence of a severe pre-existing pulmonary disease can increase the risk of overdistension. The development of a tool allowing early detection of pulmonary overdistension would represent a great asset in the prevention of VILI by allowing safer adjustments of mechanical ventilation parameters. Ultrasonographic imaging is a non-radiant, non-invasive technique already available in the intensive care setting. Already used for cardiac strain measurements, ultrasonography is a promising avenue to assess pulmonary strain.This study will aim to establish normal pleural strain values using ultrasonography in healthy volunteers.
Purpose: The primary objective is to calculate 95% confidence intervals in pleural strain for a set of 8 inspired volumes at 15 predetermined lung areas in healthy volunteers.
The secondary objectives of the study are:
* to modelize the relation between pleural strain and inspired volume
* to modelize the relation between pleural strain and global pulmonary volumetric strain
* to modelize the relation between pleural strain and maximal echo intensity change
* to compare the regional distribution pattern of pleural strain in healthy volunteers in dependent versus non-dependent areas.
Hypothesis: Elastography using the Lagrangian speckle model estimator based on optical flow allows the determination of normal mean values and 95% confidence intervals of pleural strain (average Von Mises coefficient) in 15 predetermined lung areas for a set of 8 inspired volumes in healthy volunteers.
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Participation Requirements
-
Sex:
ALL -
Eligible Ages:
18 and up
Participation Criteria
Inclusion Criteria:
* Healthy volunteers (20 men/20 women)
* 18 years old and over
* Functional capacity superior to 4 METs (metabolic equivalent of task)
Exclusion Criteria:
* Previous thoracic procedure (chest tube, thoracotomy, thoracoscopy)
* Pre-existing pulmonary disease (asthma, chronic obstructive pulmonary disease, lung fibrosis)
* Active or previous history of smoking
* Obesity (Body Mass Index superior to 30 kg/m2)
Study Location
Centre Hospitalier de l'Université de Montréal (CHUM)
Centre Hospitalier de l'Université de Montréal (CHUM)Montréal, Quebec
Canada
Contact Study Team
- Study Sponsored By
- Centre hospitalier de l'Université de Montréal (CHUM)
- Participants Required
- More Information
- Study ID:
NCT04194346