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V/Q Matching Variations With PEEP in ARDS According to Compliance-based Phenotypes (France)

Effect of PEEP on Ventilartion/Perfusion Ratios According to Different Phenotypes in Patients With ARDS (France)

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05578742
Acronym
MISMATCHED FR
Enrollment
50
Registered
2022-10-13
Start date
2024-02-08
Completion date
2026-09-30
Last updated
2025-12-08

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

Conditions

ARDS

Keywords

pulmonary perfusion, ventilation-perfusion mismatch, compliance, recruitability

Brief summary

This study aim to compare the effect of Positive End Expiratory Pressure (PEEP) on ventilation/perfusion mismatch in two phenotypes of patients with moderate-to-severe Acute Respiratory Distress Syndrome (ARDS), characterized by their respiratory system elastance (Ers). Ventilation/perfusion mismatch will be assessed by Electrical Impedance Tomography (EIT).

Detailed description

Acute Respiratory Distress Syndrome (ARDS) is characterized by hypoxemia caused by inflammatory lung injury. Recent studies showed an important variability in ARDS phenotypes . The recent COVID-19 crisis highlighted the presence of ARDS patients with severe hypoxemia and normal respiratory system compliance, and retrospective series confirmed the existence of this atypical ARDS pattern also in non-COVID etiologies. The dissociation between mechanics and hypoxemia may be related to a specific diversity in the pattern of ventilation-perfusion matching (V/Q matching) among patients with normal compliance and ARDS. In patients with low compliance, V/Q mismatch may be characterized by right-to-left shunt, secondary to collapse of the gravity-dependent regions; while, in patients with normal compliance, V/Q mismatch may show a redistribution of blood flow to hypo-ventilated lung areas by larger dead space and impaired hypoxic vasoconstriction. These differences may also influence the response to PEEP in terms of gas exchange and lung protection . It may also explain the failure for high PEEP levels to improve significantly mortality in the global ARDS population (i.e., with patients' selection only based on hypoxemia). Electrical Impedance Tomography (EIT) is a device allowing to assess ventilation and perfusion distribution. Thus, EIT can be used to evaluate global and regional V/Q matching, and could be used to understand mechanisms of hypoxemia, especially in patients with normal mechanics and ARDS. The aim of this study is to assess V/Q matching according to these different ARDS phenotypes, and to evaluate the effects of PEEP in each one.

Interventions

PROCEDUREPEEP increase

Positive End Expiratory Pressure (PEEP) will be increased from 5 to 15 cmH2O.

PROCEDUREPEEP decrease

Positive End Expiratory Pressure (PEEP) will be decreased from 15 to 5 cmH2O.

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Fifty patients will be enrolled, divided into 2 groups (n=26 each) according to a dynamic balanced sampling based on normalized respiratory system elastance (ERS) measured at PEEP 5 cmH2O with Vt 6-7 ml/kg PBW (\<2 cmH2O.mL-1.kg-1 vs. ≥2 cmH2O.mL-1.kg-1). Enrolment into each study group will be closed at 26 patients. Then, patients will be randomized and allocated to one of the following strategies: * Strategy A: PEEP 15 cmH2O → PEEP 5 cmH2O * Strategy B: PEEP 5 cmH2O → PEEP 15 cmH2O A parallel study will be conducted in Italy, to reach 50 more patients. Data will be shared between these two studies.

Eligibility

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

Inclusion criteria

* intubated patients with moderate and severe ARDS (Berlin definition, PaO2/FiO2 ≤200 mmHg at PEEP 5 cmH2O) * undergoing deep sedation * on controlled mechanical ventilation * between 24 hours and 5 days after intubation.

Exclusion criteria

* age \<18 years old; pregnancy * patient undergoing legal protection * contra-indications to EIT (e. g. severe chest trauma or wounds) * pneumothorax; patient undergoing ECMO * patient with BMI ≥35 kg/m2 * hemodynamic instability with MAP \<60 mmHg despite vasopressors.

Design outcomes

Primary

MeasureTime frameDescription
Difference in ventilation/perfusion mismatch between PEEP 5 and 15 cmH2O according to the two studied phenotypesimmediately after each interventionVentilation/perfusion (V/Q) mismatch will be assessed by Electrical Impedance Tomography (EIT). Mismatch is expressed in %. Comparison between phenotype with higher and lower elastance will be performed.

Secondary

MeasureTime frameDescription
Difference in oxygenation between PEEP 5 and 15 cmH2O according to the two studied phenotypesimmediately after each interventionPaO2 (in mmHg) will be assessed and compared between the two PEEP levels. Comparison between phenotype with higher and lower elastance will be performed.
Difference in carbon clearance between PEEP 5 and 15 cmH2O according to the two studied phenotypesimmediately after each interventionPaCO2 (in mmHg) will be assessed and compared between the two PEEP levels. Ventilatory ratio (no unit) will be derived from the PaCO2 values. Comparison between phenotype with higher and lower elastance will be performed.
Correlation between V/Q mismatch markers and recruitabilityimmediately after each interventionRecruitability will be assessed between 15 and 5 cmH2O by respiratory mechanics and EIT, as the recruited volumes value (in mL). R/I ratio will be derived from these data (no unit). V/Q mismatch will be computed by EIT, and expressed in %. Correlation will be performed by linear regression.
Difference in dead space measured by capnometric volumetry between PEEP 5 and 15 cmH2O according to the two studied phenotypesimmediately after each interventionVCO2 (measured by Vcap, in mmHg) will be assessed and compared between the two PEEP levels. Comparison between phenotype with higher and lower elastance will be performed.
Difference in respiratory mechanics between PEEP 5 and 15 cmH2O according to the two studied phenotypesimmediately after each interventionPlateau pressure and total PEEP will be aggregated to compute driving pressure (Plateau pressure minus total PEEP, all in cmH2O). Respiratory system compliance will be computed by dividing tidal volume by driving pressure (in mL.cmH2O-1; respiratory system resistance will be computed as the inverse of compliance; all these values will be assessed and compared between the two PEEP levels. Comparison between phenotype with higher and lower elastance will be performed.
Difference in venous oxygen saturation between PEEP 5 and 15 cmH2O according to the two studied phenotypesimmediately after each interventionSvO2 (in %) will be assessed and compared between the two PEEP levels. Comparison between phenotype with higher and lower elastance will be performed.
Correlations between V/Q mismatch assessed by EIT and dead space markersimmediately after each interventionDead space will be assessed by volumetric capnography (if available), venrtilatory ratio, and calorimetriy (if available). V/Q mismatch will be computed by EIT, and expressed in %. Correlation will be performed by linear regression.
Correlations between V.Q mismacth and overdisension and lung collapsusimmediately after each interventionOverdistension (%) and lung collapsus (%) will be assessed during the Step 3, by EIT. These two values cannot be measured separately. V/Q mismatch will be computed by EIT, and expressed in %. Correlation will be performed by linear regression.
Difference in stress index between PEEP 5 and 15 cmH2O according to the two studied phenotypesimmediately after each interventionstress index (no unit) will be assessed and compared between the two PEEP levels. Comparison between phenotype with higher and lower elastance will be performed.
Difference in dead space measured by calorimetry between PEEP 5 and 15 cmH2O according to the two studied phenotypesimmediately after each interventionVCO2 (measured by calorimetry, in mmHg) will be assessed and compared between the two PEEP levels. Comparison between phenotype with higher and lower elastance will be performed.

Countries

France

Contacts

Primary ContactFrançois Beloncle, MD
francois.Francois.Beloncle@chu-angers.fr+33 241 35 58 65
Backup ContactUH Angers DRCI
DRCI-Promotion-Interne@chu-angers.fr+33 2 41 35 54 96

Outcome results

None listed

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