Journal Article

Evaluating the efficacy of Seattle-PAP for the respiratory support of premature neonates: study protocol for a randomized controlled trial

Backes, Carl H., Hillman, Noah H., Zupancic, John A. F., Stenger, Michael R., Hansen, Thomas N., Notestine, Jennifer L., Lamp, Jane M., Alfred, Crystal M., Balough, Jeanne C., Howard, Christopher R., Cooper, Jennifer N., Notestine, Allison M., Kern, Juli M., Naik, Apurwa, Smith, Charles V., Rivera, Brian K., Welty, Stephen E., Miller, Randy R., Stanberry, Larissa I., Moallem, Mohannad

2019

Overview

Background At birth, the majority of neonates born at <30 weeks of gestation require respiratory support to facilitate transition and ensure adequate gas exchange. Although the optimal approach to the initial respiratory management is uncertain, the American Academy of Pediatrics endorses noninvasive respiratory support with nasal continuous positive airway pressure (nCPAP) for premature neonates with respiratory insufficiency. Despite evidence for its use, nCPAP failure, requiring intubation and mechanical ventilation, is common. Recently, investigators have described a novel method to deliver bubble nCPAP, termed Seattle-PAP. While preclinical and pilot studies are encouraging regarding the potential value of Seattle-PAP, a large trial is needed to compare Seattle-PAP directly with the current standard of care for bubble nCPAP (Fisher & Paykel CPAP or FP-CPAP). Methods/design We designed a multicenter, non-blinded, randomized controlled trial that will enroll 230 premature infants (22 0/7 to 29 6/7 weeks of gestation). Infants will be randomized to receive Seattle-PAP or FP-CPAP. The primary outcome is respiratory failure requiring intubation and mechanical ventilation. Secondary outcomes include measures of short- and long-term respiratory morbidity and cost-effectiveness. Discussion This trial will assess whether Seattle-PAP is more efficacious and cost-effective than FP-CPAP in real-world practice among premature neonates. Trial registration ClinicalTrials.gov, NCT03085329 . Registered on 21 March 2017.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Analysis / Biomedicine / Clinical trials / Consent / Continuous positive airway pressure / Continuous positive airway pressure (CPAP) / Costs / Costs analysis / Guardians / Health aspects / Health Sciences / Hypotheses / Infant / Infants / Intubation / Lungs / Medicine / Medicine & Public Health / Morbidity / Neonate / Newborn babies / Newborn infants / Pediatrics / Pregnancy / Premature babies / Premature infants / Preterm Infant / Respiratory failure / Respiratory insufficiency / Statistics for Life Sciences / Study Protocol / Surfactants / Ventilators / Welfare economics