Bovine surfactant replacement therapy in neonates of less than 30 weeks' gestation: a randomized controlled trial of prophylaxis versus treatment
- PMID: 2000278
Bovine surfactant replacement therapy in neonates of less than 30 weeks' gestation: a randomized controlled trial of prophylaxis versus treatment
Abstract
The influence of the timing of surfactant replacement therapy for the treatment of neonatal respiratory distress syndrome was evaluated in a study of 182 neonates of less than 30 weeks' gestation who were randomly assigned prior to delivery to one of three study groups: control (dummy instillation of air given at birth), early surfactant (surfactant given at birth), or late surfactant (surfactant given at less than 6 hours of age). Subjects in the late surfactant group could avoid treatment if they had a clear chest roentgenogram and required no supplemental oxygen at a mean airway pressure of less than 7 cm of water. All treated neonates were eligible to receive up to three additional doses during the first 5 days of life. The three groups were comparable with respect to birth weight, gestational age, and other perinatal parameters with the exception of a lower cord arterial pH and 1-minute Apgar score in the early surfactant group. Of the 60 neonates randomly assigned to late treatment, 29 (48%) were deemed surfactant sufficient and thereby avoided treatment; the other 31 received their first dose at a mean age of 2.9 hours. There was a significant improvement in gas exchange during the first week of life in both surfactant groups compared with the control group, reflected by differences in fraction of inspired oxygen, arterial/alveolar PO2, and ventilation index (peak pressure x rate on the ventilator) (P less than .001). Surfactant therapy also resulted in a lower incidence of pulmonary air leak and severe chronic lung disease (defined as requirement for respiratory support beyond 36 weeks post-conceptional age). There were no differences between early and late surfactant groups in any of these parameters. The only statistically significant difference between the surfactant groups was that the early group had a higher incidence of mild chronic lung disease (respiratory support beyond 28 days of age) than the late treatment group (P less than .005). Neonates in the late treatment group were extubated earlier and had a shorter neonatal intensive care unit stay than control neonates (P less than .05), whereas those in the early group were not significantly different from control neonates in these parameters. It is concluded that replacement therapy with bovine lung surfactant extract in neonates of less than 30 weeks' gestation results in decreased oxygen and ventilatory requirements during the first week of life and a lower incidence of pulmonary air leak and severe chronic lung disease.(ABSTRACT TRUNCATED AT 400 WORDS)
Similar articles
-
Single- versus multiple-dose surfactant replacement therapy in neonates of 30 to 36 weeks' gestation with respiratory distress syndrome.Pediatrics. 1990 Oct;86(4):564-71. Pediatrics. 1990. PMID: 2216622 Clinical Trial.
-
Prophylactic administration of calf lung surfactant extract is more effective than early treatment of respiratory distress syndrome in neonates of 29 through 32 weeks' gestation.Pediatrics. 1993 Jul;92(1):90-8. Pediatrics. 1993. PMID: 8516091 Clinical Trial.
-
Multicenter trial of single-dose modified bovine surfactant extract (Survanta) for prevention of respiratory distress syndrome. Ross Collaborative Surfactant Prevention Study Group.Pediatrics. 1990 Jun;85(6):1092-102. Pediatrics. 1990. PMID: 2187176 Clinical Trial.
-
[Surfactant to premature neonates].Ugeskr Laeger. 1991 Jul 29;153(31):2166-9. Ugeskr Laeger. 1991. PMID: 1866827 Review. Danish.
-
[Treatment of preterm neonates with severe respiratory distress syndrome using exogenous natural surfactants of porcine origin].An Esp Pediatr. 1992 May;36(5):375-81. An Esp Pediatr. 1992. PMID: 1616198 Review. Spanish.
Cited by
-
Pulmonary Surfactant in Adult ARDS: Current Perspectives and Future Directions.Diagnostics (Basel). 2023 Sep 15;13(18):2964. doi: 10.3390/diagnostics13182964. Diagnostics (Basel). 2023. PMID: 37761330 Free PMC article. Review.
-
The fate of exogenous surfactant in neonates with respiratory distress syndrome.Clin Pharmacokinet. 1994 Mar;26(3):215-32. doi: 10.2165/00003088-199426030-00005. Clin Pharmacokinet. 1994. PMID: 8194284 Review.
-
One-year experience in the retinopathy of prematurity: frequency and risk factors, short-term results and follow-up.Int J Ophthalmol. 2011;4(6):634-40. doi: 10.3980/j.issn.2222-3959.2011.06.12. Epub 2011 Dec 18. Int J Ophthalmol. 2011. PMID: 22553735 Free PMC article.
-
Poractant alfa versus bovine lipid extract surfactant for infants 24+0 to 31+6 weeks gestational age: A randomized controlled trial.PLoS One. 2017 May 4;12(5):e0175922. doi: 10.1371/journal.pone.0175922. eCollection 2017. PLoS One. 2017. PMID: 28472058 Free PMC article. Clinical Trial.
-
Exogenous surfactant therapy in 2013: what is next? Who, when and how should we treat newborn infants in the future?BMC Pediatr. 2013 Oct 10;13:165. doi: 10.1186/1471-2431-13-165. BMC Pediatr. 2013. PMID: 24112693 Free PMC article. Review.