Prone Positioning in Pediatric Acute Lung Injury
Overview
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- National Institute of Nursing Research (NINR)
- Enrollment
- 102
- Locations
- 1
- Primary Endpoint
- Prone positioning versus supine positioning in determining ventilator-free days in infants and children
Overview
Brief Summary
The purpose of this trial is to test the hypothesis that at the end of 28 days, infants and children with acute lung injury treated with prone positioning would have more ventilator-free days than those treated with supine positioning.
Detailed Description
Multicenter, randomized, controlled clinical trial conducted from August 28, 2001 to April 23, 2004, of 102 pediatric patients from 7 US pediatric intensive care units aged 2 weeks to 18 years who were treated with supine vs. prone positioning. Randomization was concealed and group assignment was not blinded.
Patients were randomized to either supine or prone positioning within 48 hours of meeting acute lung injury criteria, with those patients in the prone group being positioned within 4 hours of randomization and remaining prone for 20 hours each day during the acute phase of their illness for a maximum of 7 days, after which they were positioned supine. Both groups were treated using lung protective ventilator and sedation protocols, extubation readiness testing, and hemodynamic, nutrition, and skin care guidelines.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 2 Weeks to 18 Years (Child, Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Age \>42 weeks post-conceptual age and \<18 years of age
- •On mechanical ventilation (defined as presence of an endotracheal/tracheostomy tube and currently using ventilator support)
- •All of the following in the same 48 hour period:
- •acute pulmonary parenchymal disease (i.e., chest radiograph report of diffuse bilateral pulmonary alveolar infiltrates)
- •mechanical ventilation for at least 1 hour and anticipated need to continue mechanical ventilation for at least 24 hours
- •at least one PaO2/FiO2 ratio \<300 (adjusted for barometric pressure: if altitude \> 1000m, then PaO2/FiO2 \<= 300x(B.P./760), regardless of mean airway pressure)
- •functional arterial catheter for blood gas analysis
Exclusion Criteria
- •Persistent hypotension (defined as systolic blood pressure of 70mmHg+(2x age in years)); i.e. patients requiring either intravenous fluids and/or increases of additional cardiotonic medications every 2 hours
- •Active bleeding that requires ongoing blood/fluid volume replacement
- •Currently on extracorporeal membrane oxygenation (ECMO)
- •Severe chronic lung disease (cystic fibrosis or bronchopulmonary dysplasia)
- •Respiratory failure presumed to be the result of cardiac disease
- •History of symptomatic or uncorrected congenital heart disease or a right to left intracardiac shunt
- •Bone marrow or lung transplant
- •Current known diagnosis of any of the following:
- •upper airway disease (i.e., tracheitis, tracheomalacia)
- •reactive airway disease (receiving beta agonists or acute doses of systemic corticosteroids)
Outcomes
Primary Outcomes
Prone positioning versus supine positioning in determining ventilator-free days in infants and children
Secondary Outcomes
No secondary outcomes reported