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Improvement of ARDS Ventilation-perfusion Matching by Prone Positioning Assessed by EIT

Recruiting
Conditions
Electrical Impedance Tomography
Acute Respiratory Distress Syndrome
Prone Position
Registration Number
NCT05765760
Lead Sponsor
Beijing Chao Yang Hospital
Brief Summary

Acute Respiratory Distress Syndrome (ARDS) is a highly lethal disease with limited treatment options. In recent years, prone position ventilation has been shown to improve the mortality rate and lung injury of ARDS patients by promoting lung recruitment, improving ventilation/perfusion (V/Q) ratio, enhancing respiratory system compliance, promoting sputum drainage, and effectively avoiding overinflation of the dorsal lung. Electrical Impedance Tomography (EIT) technology has been used to evaluate the effect of prone position ventilation on lung V/Q matching, and some studies have confirmed that prone position ventilation can improve lung V/Q matching and oxygenation index. However, previous studies were mostly case reports or small-sample physiological studies that lacked dynamic changes in lung V/Q matching during repeated prone position ventilation. Therefore, this study hypothesizes that prone position ventilation can increase lung V/Q matching in ARDS patients, and its improvement is correlated with changes in oxygenation index, invasive ventilation time, and patient prognosis. Repeated prone position ventilation can maintain lung V/Q matching at a higher level, no longer affected by changes in body position, which can accelerate pulmonary function recovery and improve the prognosis of ARDS patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
42
Inclusion Criteria
  1. Age ≥ 18 years old;
  2. meet the diagnostic criteria of Berlin's definition for ARDS;
  3. invasive ventilation time < 48h;
  4. PaO2/FiO2 < 150mmHg.
Exclusion Criteria
  1. Contraindication to the prone position;
  2. Contraindication to the EIT;
  3. Hemodynamically unstable;
  4. Patients with hypernatremia;
  5. Patients have received extracorporeal membrane oxygenation treatment.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ICU mortality28 days after enrollment

The death of patients that occurs during their stay in the ICU

Secondary Outcome Measures
NameTimeMethod
Ventilator-free days28 days after enrollment

Days without receiving invasive ventilation at day 28.

Trial Locations

Locations (1)

Beijing Chao-Yang Hospital

🇨🇳

Beijing, Beijing, China

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