Rationale: Despite the lack of clear clinical protocols, High Flow Nasal Oxygen (HFNO) is used as post-extubation respiratory support. Although HFNO seems to reduce the need for re-intubation, scepticism on its use persists as the mechanism of action in post-extubation patients remains undefined. Monitoring weaning from invasive mechanical ventilation while monitoring respiratory effort might help to determine the added value of HFNO surrounding extubation. We hypothesize that HFNO, compared to conventional oxygen therapy (COT), prevents de-recruitment of the lung and reduces respiratory effort, and so provides a physiologic clarification for the reduction in the need for reintubation. Objective: Determine the physiological effect of HFNO compared to COT in the extubation phase regarding respiratory effort and lung aeration. Study design: A physiologic, randomized clinical study comparing two standard of clinical care therapies. Study population: Adult patients on invasive mechanical ventilation (IMV) for \>72 hours, who are scheduled for extubation. Intervention (if applicable): Before extubation, patients are randomized to receive COT (reference group) or HFNO as oxygenation regimen after extubation. Main study parameters/endpoints: The main outcome is the difference in change in lung respiratory muscle effort (mean ΔPES) at 24 hours post-extubation between the study groups. Secondary parameters are differences in changes in respiratory effort at 2 and 4 hours post-extubation, difference in change in lung aeration (mean ΔEELI), differences in tidal volume, dyspnea score, and respiratory and sputum parameters between patients undergoing different post-extubation oxygenation regimens.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
42
Flow 60L/minute. FiO2 according to clinical protocol. Temperature highest tolerated by patient, starting with 37 degrees Celsius.
Nasal Cannula, Venturi Mask or Non-rebreathing mask, according to local clinical protocols
Erasmus MC
Rotterdam, Netherlands
Maasstad Ziekenhuis
Rotterdam, Netherlands
delta Esophageal Pressure (ΔPES)
The difference between groups in change in ΔPES in patients 24 hours post-extubation.
Time frame: At 24 hours after extubation
ΔPES
The difference between groups in change in ΔPES after extubation
Time frame: At 2 and 4 hours post-extubation
delta global End-expiratory lung impedance (∆EELIglobal)
Difference between the groups in change in mean ∆EELIglobal
Time frame: At 2, 4 and 24 hours after extubation
Pressure-time product of Esophageal Pressure (PTPES)
The difference between the groups in mean pressure-time product (PTPES) compared to baseline.
Time frame: At 2,4 and 24 hours after extubation
EIT parameters
∆VARt, ∆EELIdependent, ∆EELInon-dependent compared to baseline (impedance on IMV).
Time frame: At 2, 4 and 24 hours after extubation
Global Inhomogeneity index
Time frame: At 2, 4 and 24 hours after extubation
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