The 2020 pandemic of the coronavirus (SARS-CoV2) has lead to an increase in ARDS cases requiring invasive mechanical ventilation in the ICU (Intensive Care Unit). The investigators hypothesize that airway pressure release ventilation (APRV) could be beneficial in patients with ARDS secondary to SARS-COV2 viral pneumonia.
Lung protective mechanical ventilation is the cornerstone of ARDS management, reducing the work of respiratory muscles and optimizing gas exchange. However, it can be the source of deleterious effects, grouped under the terms of ventilator induced lung injury (VILI) and ventilator induced diaphragm dysfunction. The protective ventilatory strategy has led to a significant improvement in the prognosis of ARDS patients, by reducing the volume of the air and oxygen mixture (lower tidal volume) delivered to the lungs and thus reducing the pulmonary stress and strain. However, this protective ventilation usually requires deep sedation and neuromuscular blockade to avoid deleterious patient-ventilator asynchrony. Airway Pressure Release Ventilation (APRV) has been proposed to reduce patient-ventilator asynchrony and reduce the VILI. The operating principles of APRV are based on the presence of two pressure levels that are kept constant. Spontaneous breathing is possible at any time at both pressure levels if the patient is not deeply sedated or under neuromuscular blockade. The investigators hypothesize that APRV mode could be beneficial on oxygenation and respiratory work in patients with ARDS secondary to SARS-COV2 viral pneumonia.
Study Type
OBSERVATIONAL
Enrollment
17
Ventilator management strategy
Centre Hospitalier Régional Universitaire de Nancy
Nancy, France
Proportion of patients improving PaO2/FiO2 ratio at 6 hours of APRV
Increase of at least 20% of the PaO2/FiO2 ratio
Time frame: 6 hours after starting APRV
Number of interventions on ventilator settings
Number of interventions by the physician on APRV settings
Time frame: 6 hours after starting APRV
Change in mean blood pressure
Variations of blood pressure in millimeters of mercury
Time frame: 6 hours after starting APRV
Change in heart rate
Variations of heart rate in beats per minute
Time frame: 6 hours after starting APRV
Changes in catecholamine doses
Variations of catecholamine doses in milligrams per hours
Time frame: 6 hours after starting APRV
Changes in static compliance at the end of 6 hours of APRV
Static compliance (Cstat) defined as : Cstat = (VT/(Pplat-PEPtot)) Tidal Volume (VT), Plateau pressure (Pplat) and Total Positive End-expiratory Pressure (PEEPtot)
Time frame: 6 hours after starting APRV
Variations of minute ventilation
Minute ventilation in liters per minute
Time frame: 6 hours after starting APRV
Changes in static compliance 4 hours after stopping APRV
Static compliance (Cstat) defined as : Cstat = (VT/(Pplat-PEPtot)) Tidal Volume (VT), Plateau pressure (Pplat) and Total Positive End-expiratory Pressure (PEEPtot)
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Time frame: 4 hours after starting APRV
Proportion of patients with a decrease of the PaO2/FiO2 ratio
Percentage of patients with a decrease of the PaO2/FiO2 ratio
Time frame: 4 hours after stopping APRV