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Evaluate the Effect of Prone Ventilation on Ventilated-blood Flow Ratio in Patients With ARDS by EIT

Evaluate the Effect of Prone Ventilation on Ventilated-blood Flow Ratio in Patients With Acute Respiratory Distress Syndrome by Electrical Impedance Tomography

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06181539
Enrollment
94
Registered
2023-12-26
Start date
2023-12-30
Completion date
2025-07-01
Last updated
2025-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Respiratory Distress Syndrome, Electrical Impedance Tomography, Prone Position Ventilation, Ventilation Perfusion Mismatch

Keywords

Acute Respiratory Distress Syndrome, Electrical impedance tomography, prone position ventilation

Brief summary

Patients with ARDS often suffer a gravity-dependent alveolar collapse, resulting in a reduction of tidal volume, residual alveolar excessive distension, and ventilator-related lung injury(VILI) induced by unreasonable ventilator setting.Prone ventilation (PPV) improves the gravity-dependent alveolar ventilation and promotes lung recruitment in the gravity-dependent area and improves lung compliance. Previous studies showed that prolonged PPV combined with low tidal volume(LTV) lung protected ventilation can significantly reduce the mortality of patients with moderate to severe ARDS.Although more than 60% of patients with moderate to severe ARDS due to COVID-19 has been widely implemented PPV,studies showed an improvement in oxygenation in patients with ARDS(the P/F radio improved by more than 20% before and after PPV) was 9-77%, that is, That is, some patients are unresponsive to PPV. In addition, some patients showed CO2 responsiveness after PPV(ventilation rate (VR) decreased significantly after PPV).The tools for monitoring the effects of PPV on ventilation and blood flow at bedside are still lacking, Electrical impedance tomography (EIT) is a non-invasive, non-radiative, real-time bedside lung imaging technique that can monitor local lung ventilation distribution. This study intends to use EIT to evaluate pulmonary ventilation, blood flow distribution and local V/Q ratio before and after PPV, as well as to monitor the changes in pulmonary physiology before and after PPV, explore the mechanism of PPV improving oxygenation by combined with the changes in oxygenation, and explore the factors that predict and affect PPV responsiveness.

Detailed description

Acute respiratory distress syndrome (ARDS) is presented as acute hypoxemia and pulmonary edema due to the increased permeability of alveolar capillaries. Endothelial damage injury and swelling, microthrombosis, and hypoxic pulmonary vasoconstriction can lead to low pulmonary blood vessels perfusion and even occlusion, while patients with ARDS often suffer a gravity-dependent alveolar collapse, resulting in a reduction of tidal volume, residual alveolar excessive distension, and ventilator-related lung injury(VILI) induced by unreasonable ventilator setting.Prone ventilation (PPV) improves the gravity-dependent alveolar ventilation and promotes lung recruitment in the gravity-dependent area and improves lung compliance. Besides, pulmonary blood perfusion is less affected by gravity distribution, thus the improvement of gravity-dependent alveolar ventilation can significantly reduce shunt, and lung heterogeneity and improve V/Q radio. Previous studies showed that prolonged PPV combined with low tidal volume lung protected ventilation can significantly reduce the mortality of patients with moderate to severe ARDS.Although more than 60% of patients with moderate to severe ARDS due to COVID-19 has been widely implemented PPV,studies showed an improvement in oxygenation in patients with ARDS(the P/F radio improved by more than 20% before and after PPV) was 9-77%, that is, That is, some patients are unresponsive to PPV. In addition, some patients showed CO2 responsiveness after PPV (ventilation rate (VR) decreased significantly after PPV).The tools for monitoring the effects of PPV on ventilation and blood flow at bedside are still lacking, Electrical impedance tomography (EIT) is a non-invasive, non-radiative, real-time bedside lung imaging technique that can monitor local lung ventilation distribution. By injecting hypertonic saline through a central vein catheter, we can obtain lung perfusion images to indicate local lung blood flow distribution. In addition, combined with lung ventilation images, we can evaluate the pulmonary shunt, dead space, V/Q ratio, to better clarify the physiological and pathological status of lung.This study intends to use EIT to evaluate pulmonary ventilation, blood flow distribution and local V/Q ratio before and after PPV, as well as to monitor the changes in pulmonary physiology before and after PPV, explore the mechanism of PPV improving oxygenation by combined with the changes in oxygenation, and explore the factors that predict and affect PPV responsiveness.

Interventions

None listed

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 1\. Age ≥18 years. 2. Patients diagnosed with ARDS according to the Berlin definition and need to endotracheal intubated and mechanical ventilated in prone position within 48 hours of endotracheal intubation 3. PaO2/FiO2 \< 150 mmHg with positive end-expiratory pressure (PEEP) ≥ 5 cmH2O according to the Berlin definition.

Exclusion criteria

* 1\. Contraindications of EIT such as chest wound dressing, installation of pacemaker, defibrillator, etc. 2\. Unstable vertebral fracture 3. Within 15 days after severe facial trauma or facial surgery 4 within 15 days after tracheal surgery or sternotomy 5. Hemodynamic instability or recent cardiac arrest 6. Increased intraocular pressure. 7. Unstable femoral or pelvic fractures and pelvic external fixation. 8 He had severe chest wall disease and unstable rib fractures. 9 Recent cardiothoracic surgery. 10. Pneumothorax 11. Chronic lung disease: severe obstructive pulmonary disease, severe asthma, interstitial lung disease. 12\. Maternal 13. Extracorporeal membrane oxygenation(ECMO) had been administered on admission to the ICU. 14\. Intracranial hypertension 15. Pulmonary embolism, acute or chronic right heart failure 16. Severe cardiac dysfunction (New York Heart Association class III or IV, acute coronary syndrome, or sustained ventricular tachyarrhythmia), cardiogenic shock; 17. No informed consent was obtained

Design outcomes

Primary

MeasureTime frameDescription
Pulmonary ventilation perfusion(V/Q) ratio after 16 hours of PPV monitored by EIT16 hours after prone position ventilationthe V/Q radio were monitored by EIT after patients were implemented prone position ventilation(PPV) for 16h. The images of ventilation distribution were collected by EIT, and the images of perfusion distribution were collected by injected 10ml of 10% hypertonic saline through a central vein catheter during inspiratory hold or expiratory hold. The ventilation and perfusion images were analysed by specialized software to obtain the data of V/Q radio.

Secondary

MeasureTime frameDescription
Driving pressure before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingDriving pressure(DP) data were obtained from ventilators
Pulmonary ventilation perfusion(V/Q) ratio before PPV monitored by EIT before PPVwithin 1 hour before preparing PPVThe V/Q radio were monitored by EIT before patients were implemented prone position ventilation(PPV). The images of ventilation distribution were collected by EIT, and the data of perfusion distribution were collected by injected 10ml of 10% hypertonic saline through a central vein catheter during inspiratory hold or expiratory hold. The ventilation and perfusion images were analysed by specialized software to obtain the data of V/Q radio.
Pulmonary ventilation perfusion(V/Q) ratio after PPV ending 8h monitored by EIT8 hours hours after prone position ventilation endingthe V/Q radio were monitored by EIT 8 hours after prone position ventilation ending.The images of ventilation distribution were collected by EIT, and the data of perfusion distribution were collected by injected 10ml of 10% hypertonic saline through a central vein catheter during inspiratory hold or expiratory hold. The ventilation and perfusion images were analysed by specialized software to obtain the data of V/Q radio.
Pulmonary ventilation distribution before PPV, PPV for 16h and 8h after PPV endingwithin 1hour before preparing PPV, 16 hours after and 8 hours after PPV endingPulmonary ventilation distribution were monitored by EIT before PPV, PPV for 16h and 8h after PPV ending. The images of ventilation distribution were collected by EIT and analysed by specialized software to obtain the data.
Pulmonary perfusion distribution before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingThe pulmonary perfusion distribution were monitored by EIT before PPV, PPV for 16h and 8h after PPV ending. The images of perfusion distribution were collected by injected 10ml of 10% hypertonic saline through a central vein catheter during inspiratory hold or expiratory hold. The perfusion images were analysed by specialized software to obtain the data of pulmonary perfusion distribution.
Pulmonary shunt percentage before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingThe ventilation and perfusion images were analysed by specialized software to obtain the data of pulmonary shunt percentage.
Pulmonary dead space percentage before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingThe ventilation and perfusion images were analysed by specialized software to obtain the data of pulmonary dead space percentage.
Peak pressure before PPV, PPV for 16h and 8h after PPV endingWithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingPeak pressure data were obtained from ventilators
Static compliance(Cs) before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingCs is equal to tidal volume divided by DP
Tidal volume before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingTidal volume data were obtained from ventilators
P/F ratio before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingP/F ratio data were obtain from arterial blood gas analysis
Carbon dioxide partial pressure(PaCO2) before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingPaCO2 data were obtain from arterial blood gas analysis
Ventilatory ratio(VR) before PPV, PPV for 16h and 8h after PPV endingwithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingVR=\[minute ventilation (ml/min)×arterial partial tension of carbon dioxide (mmHg)\] / \[predicted body weight×100×37.5
28 days mortalityFrom the day of enrollment to day 28Mortality of from the day of enrollment to day 28
Ventilator free days(VFD) within 28 daysFrom the day of enrollment to day 28The number of ventilator free days for patients from enrollment day to day 28, if patients died within 28 days,VFD was equal to zero.
Mortality in the ICUFrom the day of enrollment to the day of transfer from the ICU or death,up to 90 daysMortality in the ICU of all participants
Length of stay(LOS)From the day of to the day of admitting to hospital to depart from the hospital or death,up to 90 daysLOS(length of stay) of hospital
Plat pressure before PPV, PPV for 16h and 8h after PPV endingWithin 1 hour before preparing PPV, 16 hours after and 8 hours after PPV endingPlat pressure data were obtained from ventilators

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026