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ABSTRACT: Objectives
To compare the efficacy and safety of poractant alfa and bovine lipid extract surfactant in preterm infants.Study design
Randomized, partially-blinded, multicenter trial. Infants <32 weeks needing surfactant before 48 hours were randomly assigned to receive poractant alfa or bovine lipid extract surfactant. The primary outcome was being alive and extubated at 48 hours post-randomization. Secondary outcomes included need for re-dosing, duration of respiratory support and oxygen, bronchopulmonary dysplasia, mortality and complications during administration.Results
Three centers recruited 87 infants (mean 26.7 weeks and 906 grams) at a mean age of 5.9 hours, between March 2013 and December 2015. 21/42 (50%) were alive and extubated at 48 hours in the poracta
SUBMITTER: Lemyre B
PROVIDER: S-EPMC5417427 | biostudies-literature | 2017
REPOSITORIES: biostudies-literature