High-frequency Oscillatory Ventilation (HFOV) in Preterm Infants With Severe Respiratory Distress Syndrome (RDS)
Respiratory Distress Syndrome
About this trial
This is an interventional prevention trial for Respiratory Distress Syndrome focused on measuring high-frequency oscillatory ventilation, respiratory distress syndrome, preterm infants, neurodevelopment, preterm infants with severe respiratory distress syndrome
Eligibility Criteria
Inclusion Criteria:
- Preterm infants admitted to the NICU with gestational age <32 weeks, birth weight <1500g and less than 24 hours of age
- Who developed RDS requiring mechanical ventilation
- Presented a partial pressure of oxygen (PaO2): fraction of inspired oxygen (FIO2) ratio <200
- Radiograph criteria of severe RDS
Exclusion Criteria:
- Infants with genetic metabolic diseases
- Congenital abnormalities
- Pneumothorax
- Grade III-IV intracranial hemorrhage
Sites / Locations
- Zhengzhou Children's Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
HFOV
CV
A SLE5000 infant ventilator was used as the high-frequency ventilator.HFOV setting were as follows: initial frequency was set between 11 and 15Hz; pressure amplitude of oscillation was initially adjusted to provide adequate chest wall movement and was subsequently titrated to maintain the PaCO2 between 40 and 55 mmHg.Extubation was considered when the patient's condition was stable for 12-24h, while adequate oxygenation could be maintained with an FIO2 <0.3 and respiratory rate <25/min.
A Servo-i-Maquet will be used as the conventional mechanical ventilator. CV settings were: exhaled tidal volumes set at 5-6 mL/kg, initial peak inspiratory pressure (PIP) of 15-25 cmH2O; positive expiratory end pressure (PEEP) set to 4-6 cmH2O; inspiratory times of 0.25-0.40s; rates set to <60/min. The weaning process was initiated when the following parameters were achieved: PIP <18 cmH2O, PEEP <4 cmH2O, and FIO2 <0.4. Extubation was considered when the patient's condition was stable for 12-24h, while adequate oxygenation could be maintained with an FIO2 <0.3 and respiratory rate <25/min. All infants extubated onto nasal continuous positive airway pressure (Infant Flow, Electro Medical Equipment) and then weaned to a nasal cannula, and then to room air.