Journal Article10.1542/PEDS.109.6.1081
A multicenter, randomized, controlled trial comparing Surfaxin (Lucinactant) lavage with standard care for treatment of meconium aspiration syndrome.
Thomas E. Wiswell,Gail Knight,Neil N. Finer,Steven M. Donn,Hemant Desai,William F. Walsh,Krishnamurthy Sekar,Graham Bernstein,Graham Bernstein,Martin Keszler,Martin Keszler,Valya E. Visser,Valya E. Visser,Valya E. Visser,T. Allen Merritt,T. Allen Merritt,Frank L. Mannino,Lisa Mastrioianni,Lisa Mastrioianni,Brian Marcy,Brian Marcy,Susan D. Revak,Huei Tsai,Huei Tsai,Charles G. Cochrane +24 more
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TL;DR: Dilute Surfaxin lavage seems to be a safe and potentially effective therapy in the treatment of MAS, and data from this investigation support future prospective, controlled clinical trials of bronchoalveolar lavage withSurfaxin in neonates with MAS.
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Abstract: Objective. Infants with meconium aspiration syndrome (MAS) have marked surfactant dysfunction. Airways and alveoli of affected neonates contain meconium, inflammatory cells, inflammatory mediators, edema fluid, protein, and other debris. The objective of this study was to compare treatment with bronchoalveolar lavage using dilute Surfaxin with standard therapy in a population of newborn infants with MAS. Methods. Inclusion criteria were 1) gestational age ≥35 weeks, 2) enrollment within 72 hours of birth, 3) diagnosis of MAS, 4) need for mechanical ventilation, and 5) an oxygenation index ≥8 and ≤25. Subjects were randomized to either lavage with Surfaxin or standard care (2:1 proportion). In lavaged infants, a volume of 8 mL/kg dilute Surfaxin (2.5 mg/mL) was instilled into each lung over approximately 20 seconds followed by suctioning after 5 ventilator breaths. The procedure was repeated twice. The third and final lavage was with a more concentrated solution (10 mg/mL) of Surfaxin. Results. Twenty-two infants were enrolled (15 Surfaxin and 7 control). Demographic characteristics were similar. There were trends (not significant) for Surfaxin-lavaged infants to be weaned from mechanical ventilation earlier (mean of 6.3 vs 9.9 days, respectively), as well as to have a more rapid decline in their oxygenation indexes compared with control infants, the latter difference persisting for the 96-hour-long study period. The therapy was safe and generally well tolerated by the infants. Conclusions. Dilute Surfaxin lavage seems to be a safe and potentially effective therapy in the treatment of MAS. Data from this investigation support future prospective, controlled clinical trials of bronchoalveolar lavage with Surfaxin in neonates with MAS.
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Surfactant-Replacement Therapy for Respiratory Distress in the Preterm and Term Neonate
TL;DR: Because respiratory insufficiency may be a component of multiorgan dysfunction, preterm and term infants receiving surfactant-replacement therapy should be managed in facilities with technical and clinical expertise to administer surfactants and provide multisystem support.
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An overview of pulmonary surfactant in the neonate: Genetics, metabolism, and the role of surfactant in health and disease
TL;DR: Gene therapy could prove valuable in treating inherited defects of surfactant metabolism, which results in respiratory distress with attendant morbidity and mortality in newborns and preterm children.
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A multicenter, randomized, controlled trial of lucinactant versus poractant alfa among very premature infants at high risk for respiratory distress syndrome.
Sunil K. Sinha,Sunil K. Sinha,Thierry Lacaze-Masmonteil,Adolf Valls i Soler,Thomas E. Wiswell,Janusz Gadzinowski,Júlia Hajdú,Graham Bernstein,Manuel Sánchez-Luna,Robert Segal,Christopher Schaber,Joseph M. Massaro,Ralph B. D'Agostino +12 more
TL;DR: Lucinactant and poractant alfa were similar in terms of efficacy and safety when used for the prevention and treatment of RDS among preterm infants, with the lower boundary of the 95% CI for the difference being greater than the prespecified noninferiority margin.
190
Meconium aspiration syndrome: historical aspects.
TL;DR: The management of babies delivered with associated MSAF before the accumulation of evidence for best practice through appropriately powered, prospective randomized controlled trials is detailed.
151
Surfactant for meconium aspiration syndrome in full term/near term infants.
TL;DR: In infants with MAS, surfactant administration may reduce the severity of respiratory illness and decrease the number of infants with progressive respiratory failure requiring support with ECMO.
128
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Meconium-stained amniotic fluid and the meconium aspiration syndrome. An update.
TL;DR: The authors review the current status of knowledge concerning the MSAF and MAS and management of these entities.
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Surfactant Replacement Therapy for Meconium Aspiration Syndrome
TL;DR: Surfactant replacement therapy, if started within 6 hours after birth, improves oxygenation and reduces the incidence of air leaks, severity of pulmonary morbidity, and hospitalization time of term infants with MAS.
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Multicenter study of surfactant (beractant) use in the treatment of term infants with severe respiratory failure
A. Lotze,B. R. Mitchell,D. I. Bulas,E. M. Zola,R. A. Shalwitz,J. H. Gunkel,H. Feick,J. Fasules,M. Magoon,T. Weber,K. P. Van Meurs,L. Salter,A. Thompson,S. Pearlman,M. Rodriguez,D. Hsiao,R. Miller,J. McGowan,G. Waterkotte,F. Murphey,R. Baker,B. Patel,M. Keszler,J. Ferlauto,W. Engle,D. Stewart,J. Bhatia,W. Kanto,K. B. Al-Mateen,D. Purohit,C. Dothey,M. Fernandes,J. Gerdes,M. Shwer,E. Stork,D. Marsh,J. Gonzalez,M. Maurer,D. Sprague,G. Knight,P. Riedel,L. Parton,M. Antunes,E. Rider,D. J. Rawlings,W. Drummond,D. Kays,S. Denson,J. Sparks,S. Keeney,S. St. Charles,R. Cicco +51 more
TL;DR: Use of surfactant, particularly in the early phase of respiratory failure, significantly decreases the need for ECMO in the treatment of term newborns with respiratory failure and without increasing the risk of complications.
335
•Journal Article
Surfactant treatment of full-term newborns with respiratory failure.
TL;DR: Patients with respiratory failure associated with pneumonia and meconium aspiration syndrome were treated with 90 mg/kg of a calf lung surfactant extract, given intratracheally up to every 6 hours for a maximum of four doses to show significant improvement in oxygenation.
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