Low tidal volume ventilation (LTV) has been proposed and widely used in patients with acute respiratory distress syndrome (ARDS) to prevent ventilator-induced lung injury (VILI) and mitigate its effects. The LTV strategy is intended to protect the "baby lung" from overdistension while simultaneously allowing acutely injured tissue to continually collapse. Airway pressure release ventilation (APRV) is a highly effective strategy improving lung recruitment and oxygenation in clinical studies, but its effects on lung injury and mortality is debatable. Animal studies revealed that APRV could normalize post-injury heterogeneity and reduce the risk of VILI. Our objective was to investigate the impact of APRV and LTV on regional ventilation and perfusion distribution in ARDS patients by electrical impedance tomography (EIT).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Patients with moderate-to-severe ARDS were supported with APRV.
Patients with moderate-to-severe ARDS were supported with LTV.
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, China
RECRUITINGLung ventilation/perfusion matching
Lung ventilation/perfusion matching assessed by EIT
Time frame: 24hour
Lung ventilation distrubution
Lung ventilation distrubution assessed by EIT
Time frame: up to 72hour
Lung perfusion distrubution
Lung perfusion distrubution assessed by EIT
Time frame: up to 72hour
Dead-space% and shunting%
Lung Dead-space% and shunting% assessed by EIT
Time frame: up to 72hour
Oxygenation index
Oxygenation index=Arterial partial pressure of oxygen /fraction of inspired oxygen
Time frame: up to 72hour
Arterial partial pressure of carbon dioxide (PaCO2)
PaCO2 is one of the key indicators of pulmonary ventilation which can be obtained from arterial blood gas analysis.
Time frame: up to 72hour
Static respiratory compliance (Crs)
Crs=tidal volume/driving pressure
Time frame: up to 72hour
Cardiac output
Cardiac output assessed by echocardiography
Time frame: up to 72hour
Right ventricular function
Right ventricular function assessed by echocardiography
Time frame: up to 72hour
Ventilator free days
28d-ventilator free days after randomization
Time frame: up to 28days
Duration of Intensive care units stay
28d-duration of Intensive care units stay after randomization
Time frame: up to 28days
Mortality after randomization
28d-all-cause mortality
Time frame: up to 28days
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