Infants With Severe Acute Respiratory Distress Syndrome: The Prone Trial
Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS), Surfactant Dysfunction, Infant
About this trial
This is an interventional treatment trial for Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS) focused on measuring Acute Respiratory Distress Syndrome, Electrical Impedance Tomography, Lung Ultrasonography, Prone Position, Infants
Eligibility Criteria
Inclusion Criteria:
- Patients hospitalized at Pediatric Intensive Care Unit (PICU) or Neonatal Intensive Care Unit (NICU) of the Medical University Vienna.
- Patients aged >36 weeks (corrected gestational age) and <24 months.
- Patient intubated and mechanically ventilated for at least 6 hours, with an expected requirement of invasive ventilatory support for at least 12 hours.
- Clinical picture strongly suggestive for acute bronchiolitis or pneumonia (fever, fine crackles, prolonged expiration, lung hyperinflation and/or findings of new infiltrates consistent with acute pulmonary parenchymal disease on chest X-ray).
- Severe pediatric acute respiratory distress syndrome (ARDS), defined by OSI ≥12.3 (wean FIO2 to maintain SpO2 ≤ 97% to calculate oxygen saturation index).
- Written informed consent obtained from parents.
Exclusion Criteria:
Clinical context
- Need for O2 supplementation to maintain SpO2>94% in the 4 weeks preceding hospitalization in the PICU/NICU
- Cyanotic congenital heart disease Cardiogenic pulmonary edema
- Severe pulmonary hypertension
- Untreated pneumothorax
- Severe neurological abnormalities
- Other severe congenital anomalies such as congenital diaphragmatic hernia
- Ongoing cardiopulmonary resuscitation or limitation of life support
Contradictions for prone positioning (adapted from Guerin, C., et al., Prone positioning in severe acute respiratory distress syndrome. N Engl J Med, 2013. 368(23): p. 2159-68):
- Intracranial pressure >30 millimeters of mercury (mmHg) in supine position or cerebral perfusion pressure <60 mmHg
- Massive hemoptysis requiring an immediate surgical or interventional radiology procedure
- Tracheal surgery or sternotomy during the previous 15 days
- Serious facial trauma or facial surgery during the previous 15 days
- Deep venous thrombosis treated for less than 2 days
- Cardiac pacemaker inserted in the last 2 days
- Unstable spine, femur, or pelvic fractures
- Use of extracorporeal membrane oxygenation (ECMO) before inclusion
- Lung transplantation
- Burns on more than 20% of the body surface
Other non-inclusion criteria
- Indication not to attempt resuscitation
- Patient already recruited for other clinical studies
- Patients who already received surfactant in the last 4 weeks
- Thoracic skin lesions or wounds on the thorax, where the EIT-electrode-belt would be placed
Sites / Locations
- Medical University of ViennaRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Prone Group
Supine Group
Turn patient in prone position after surfactant administration. After 6 hours turn patient in supine position and perform EIT and LUS.
Leave patient in supine position after surfactant administration. After 6 hours perform EIT and LUS.