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Study Goal The goal of this observational, multicenter study is to evaluate how positive end-expiratory pressure (PEEP) affects right ventricular (RV) function in patients with acute respiratory distress syndrome (ARDS) who are receiving mechanical ventilation. Researchers will assess the Recruitment-to-Inflation (R/I) ratio, a measurement used to determine whether increasing PEEP helps open the lungs or causes harmful effects on the heart and circulation.
Main Study Questions
This study aims to answer the following questions:
Who Can Participate?
Patients will be included in the study if they meet the following criteria:
Patients will not be included in the study if they:
Study Procedures
Participants will undergo a series of tests to measure the impact of PEEP on lung and heart function:
Initial Airway Closure Test: Patients will be evaluated while on a low PEEP level of 5 cmH₂O for 10 minutes to confirm eligibility.
Recruitment-to-Inflation (R/I) Ratio Assessment:
Echocardiographic Heart Function Assessment:
Data Collection:
oKey respiratory and hemodynamic parameters will be recorded, including heart strain, cardiac output, pulmonary artery pressure, and venous congestion.
Primary and Secondary Study Outcomes
Primary Outcome: The study will evaluate how RV function changes in response to different PEEP levels, using 2D RV strain measurements as a key indicator.
Secondary Outcomes: Researchers will assess:
Statistical Analysis
Study Size and Impact The study aims to enroll 60 patients (30 per group) to ensure that results are reliable. This sample size was calculated to detect at least a 10% change in RV strain, with a 90% probability of identifying significant effects.
Expected Benefits of the Study This study will help critical care doctors better understand how to adjust PEEP settings to balance lung recruitment and heart function in ARDS patients. By identifying the best methods to detect right heart dysfunction early, this research could lead to improved ventilation strategies and better survival outcomes for patients with severe lung injury.m
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60 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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