Avalanches and power-law behaviour in lung inflation.
B Suki, A L Barabási, Z Hantos...
https://pubmed.ncbi.nlm.nih.gov/8145846Actively Recruiting
Led by Poitiers University Hospital · Updated on 2025-12-24
50
Participants Needed
1
Research Sites
4 weeks
Total Duration
Acute respiratory distress syndrome (ARDS) affects many patients who require mechanical ventilation and is linked to a high risk of death. Mechanical ventilation, while life-saving, can worsen lung injury through lung overdistension and repeated airway opening and closing, known as atelectrauma. This study investigates a phenomenon called the "avalanche" effect during airway opening in ARDS, which has been suggested by animal and mathematical models but not yet observed in humans. Understanding this may help improve ventilation strategies and patient outcomes. Researchers will monitor airway pressure, flow, esophageal pressure, and ventilation distribution using electrical impedance tomography in patients with ARDS. The ventilator settings will be adjusted, including positive end-expiratory pressure set at 15 cmH2O for 10 minutes, followed by a decrease in respiratory rate and positive end-expiratory pressure to measure lung volume changes. Low-flow inflation and deflation pressure-volume curves will be performed before returning to standard ventilator settings. These procedures are part of usual care and patients will be followed until 28 days after inclusion or ICU discharge. Participants will have baseline data collected and undergo repeated assessments of lung function and ventilation mechanics. Researchers will measure the prevalence of the avalanche phenomenon during low-flow lung inflation and other lung pressure characteristics. Patient outcomes and characteristics will be compared based on the presence of this phenomenon. The study includes monitoring through measurements and imaging, with a focus on safety and collecting detailed data to better understand lung behavior in ARDS.
CONDITIONS
Avalanche Phenomenon During Airways Opening in Acute Respiratory Distress Syndrome
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 28 days or until ICU discharge
Participants who undergo routine care are observed while airway pressure, flow, esophageal pressure, and ventilation distribution are recorded during ventilator maneuvers as part of usual care for acute respiratory distress syndrome.
Total: 1 location
1
CHU Poitiers
Poitiers, France, 86000
Actively Recruiting
R
Rémi Coudroy, MD, PhD
C
Céline DELETAGE
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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B Suki, A L Barabási, Z Hantos...
https://pubmed.ncbi.nlm.nih.gov/8145846Lu Chen, Lorenzo Del Sorbo, Domenico Luca Grieco...
https://pubmed.ncbi.nlm.nih.gov/28557528