Weaning Failure Clinical Trial
Official title:
Does High Flow Nasal Cannula Oxygen Therapy Prevent Reintubation in Pediatric Surgical Intensive Care Unit
monocentric randomized controlled trial starting from Mars 2017, recruitment is still
ongoing. Patients aged between 0-45 days needing mechanical ventilation (MV) with tracheal
intubation were included random assignation in two groups for post-extubation management:
Group Optiflow (GO) for patients receiving High Flow Nasal Cannula Oxygen Therapy HNFC and
Control Group (CG) for conventional treatment.
Patients were evaluated during the first 72h following extubation. Primary endpoint was the
incidence of reintubation. Secondary endpoints were incidence of post-extubation respiratory
failure, time to reintubate and weaning time from oxygen. Respiratory and hemodynamic
parameters were assessed and compared between the two groups upon extubation, after 2 hours
(H2), at H6, H12, H24, H36, H48 and H72. Length of stay (LOS) and mortality were also
estimated.
We conducted a monocentric randomized controlled trial starting from Mars 2017, recruitment is still ongoing. Patients aged between 0-45 days needing mechanical ventilation (MV) with tracheal intubation were included regardless type of admission, severity of disease and randomly assigned in two groups for post-extubation management: Group Optiflow (GO) for patients receiving HNFC oxygen therapy and Control Group (CG) for conventional treatment. Before programmed extubation, newborns and young infants received 0.15 mg/kg of Dexamethasone. Patients were evaluated during the first 72h following extubation. Primary endpoint was the incidence of reintubation. Secondary endpoints were incidence of post-extubation respiratory failure, time to reintubate and weaning time from oxygen. Respiratory and hemodynamic parameters were assessed and compared between the two groups upon extubation, after 2 hours (H2), at H6, H12, H24, H36, H48 and H72. Length of stay (LOS) and mortality were also estimated. ;
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