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Clinical Trials/NCT05781802
NCT05781802
Recruiting
Not Applicable

Assessment of V/Q Matching During Pressure Support Ventilation With Electrical Impedance Tomography

Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo1 site in 1 country15 target enrollmentFebruary 27, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Respiratory Failure
Sponsor
Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo
Enrollment
15
Locations
1
Primary Endpoint
Changes in ventilation-perfusion matching
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

The aim of this study is to describe the effects of different levels of pressure support on ventilation-perfusion matching in patients recovering from ARDS, using electrical impedance tomography.

Detailed Description

Spontaneous breathing during mechanical ventilation has been attributed to both protective and negative effects on patient outcomes, largely varying based on the severity of lung injury. Indeed, in severe ARDS the avoidance of spontaneous efforts has an established protective role. However, spontaneous breathing promotes the distribution of tidal volume towards the dependent lung, and low levels of support pressure determine more homogeneous ventilation in patients recovering from ARDS, compared to higher support levels. Physiology supports the potential of spontaneous breathing to increase lung perfusion, through the decrease of intra-thoracic pressure leading to an increased venous return. This mechanism, in absence of right ventricular dysfunction, may lead to increased global lung perfusion. Furthermore, gas exchange improvements in experimental lung injury models during pressure support vs. controlled ventilation have been explained with redistribution of lung perfusion to nondependent lung areas and improvement of V/Q matching even in absence of significant lung recruitment. Electrical impedance tomography has been clinically used as a non-invasive tool to assess V/Q matching in patients with ARDS and to compare V/Q matching prior to and after a cycle of prone position in spontaneously breathing patients with COVID-19. The aim of this study is to describe the effects of different levels of pressure support on ventilation-perfusion matching in patients recovering from ARDS, using electrical impedance tomography.

Registry
clinicaltrials.gov
Start Date
February 27, 2023
End Date
January 1, 2024
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo
Responsible Party
Principal Investigator
Principal Investigator

Andrea Cortegiani, MD

Clinical Professor

Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years
  • Need for invasive mechanical ventilation and ICU admission
  • Diagnosis of ARDS at ICU admission or during ICU stay
  • Informed consent
  • Presence of central line in the internal jugular vein

Exclusion Criteria

  • Any contraindication to Electrical impedance tomography monitoring (e. g. severe chest trauma or wounds)
  • Cardiogenic pulmonary edema
  • Pulmonary embolism
  • Chronic obstructive pulmonary disease
  • Pulmonary fibrosis
  • Asthma exacerbation
  • Pneumothorax and/or chest drainages
  • Pre-existing diaphragmatic function impairment
  • Neuro-muscular disease or impairment
  • Moribund patients with limitation of care or expected survival \<48h according to the treating physician

Outcomes

Primary Outcomes

Changes in ventilation-perfusion matching

Time Frame: Measured after at least 20 minutes from the application of each of the levels of pressure support and at clinical stability

Changes in ventilation-perfusion matching between the two different levels of pressure support ("high" level of pressure support and "low" level of pressure support)

Secondary Outcomes

  • Changes in regional ventilation distribution(Measured after at least 20 minutes from the application of each of the levels of pressure support and at clinical stability)
  • Changes in regional perfusion distribution(Measured after at least 20 minutes from the application of each of the levels of pressure support and at clinical stability)
  • Changes in gas exchange(Measured after at least 20 minutes from the application of each of the levels of pressure support and at clinical stability)

Study Sites (1)

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