The main objective of this study is to evaluate the gas exchange (ventilation-perfusion ratio) with the system Optiflow® compared to facial mask among patients having an acute respiratory failure after cardiac surgery.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
90
J0: randomization (Optiflow® or facial mask), lung X-ray, kinesiotherapy H0 : clinical examination, blood gas, respiratory frequency H1 : clinical examination, blood gas, respiratory frequency H6 : clinical examination, blood gas J1: clinical examination, blood gas, respiratory frequency, lung X-ray, diaphragmatic echography, kinesiotherapy J2: clinical examination, blood gas, lung X-ray, kinesiotherapy Follow-up (until withdrawal of Optiflow or facial mask): clinical examination, blood gas, lung X-ray, kinesiotherapy
Nantes University Hospital
Nantes, France
Measure of PaO2/FiO2 ratio
The main objective of this study is to evaluate the gas exchange (ventilation-perfusion ratio) with the system Optiflow® compared to facial mask among patients having an acute respiratory failure after cardiac surgery.
Time frame: One hour and 24 hours
Scale of satisfaction completed by the patient
To evaluate the tolerance of high flow oxygen therapy: satisfaction scale
Time frame: at withdrawal of oxygen system
Measure of pH, SatO2, PaO2, FiO2
To evaluate hypoxia duration
Time frame: 2 days
Number of days of hospitalization
To evaluate the duration of hospitalization with the medical device
Time frame: at day 28
Measure of PCO2 and respiratory frequency
To evaluate PCO2 and respiratory frequency at H+1 and J1
Time frame: One day
Possibility of patient transfer in conventional service
To evaluate the reception in post reanimation if transfer under oxygen therapy
Time frame: at day 5
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