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Two-year outcome data suggest that less invasive surfactant administration (LISA) is safe. Results from the follow-up of the randomized controlled AMV (avoid mechanical ventilation) study.
Herting, Egbert; Kribs, Angela; Härtel, Christoph; von der Wense, Axel; Weller, Ursula; Hoehn, Thomas; Vochem, Matthias; Möller, Jens; Wieg, Christian; Roth, Bernhard; Göpel, Wolfgang.
Afiliación
  • Herting E; Department of Paediatrics, University Hospital of Schleswig-Holstein, University of Lübeck, Ratzeburger Allee 160, D-23538, Lübeck, Germany. egbert.herting@uksh.de.
  • Kribs A; Department of Neonatology, University of Cologne, Cologne, Germany.
  • Härtel C; Department of Paediatrics, University Hospital of Schleswig-Holstein, University of Lübeck, Ratzeburger Allee 160, D-23538, Lübeck, Germany.
  • von der Wense A; Department of Neonatology, Children's Hospital Hamburg-Altona, Hamburg, Germany.
  • Weller U; Department of Paediatrics, Evangelical Klinikum Bethel, Bielefeld, Germany.
  • Hoehn T; Department of Paediatrics, University of Düsseldorf, Düsseldorf, Germany.
  • Vochem M; Department of Neonatology, Olgahospital Stuttgart, Stuttgart, Germany.
  • Möller J; Department of Paediatrics, Saarbrücken General Hospital, Saarbrücken, Germany.
  • Wieg C; Germany Children's Hospital Aschaffenburg-Alzenau, Aschaffenburg, Germany.
  • Roth B; Department of Neonatology, University of Cologne, Cologne, Germany.
  • Göpel W; Department of Paediatrics, University Hospital of Schleswig-Holstein, University of Lübeck, Ratzeburger Allee 160, D-23538, Lübeck, Germany.
Eur J Pediatr ; 179(8): 1309-1313, 2020 Aug.
Article en En | MEDLINE | ID: mdl-32067100
ABSTRACT
Less invasive surfactant administration (LISA) is a method to deliver surfactant to spontaneously breathing premature infants via a thin catheter. Here we report the two-year outcome from the AMV (avoid mechanical ventilation) study, the first randomized controlled trial on this mode of surfactant delivery. No statistically significant differences in weight, length or neurodevelopmental outcome (Bayley II scores) were found between the LISA intervention group (n = 95) and the control group (n = 84) that received standard treatment.

Conclusion:

No differences in outcome were observed at 2 years. LISA seems safe in that aspect. What is Known • LISA is a method that is in increasing use for surfactant delivery to spontaneously breathing infants. LISA reduces the need for mechanical ventilation. What is New • Outcome data at 2 years from the first randomized study with LISA raise no safety concerns in comparison to a group of infants that received standard treatment.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Dificultad Respiratoria del Recién Nacido / Surfactantes Pulmonares / Trastornos del Neurodesarrollo / Trastornos del Crecimiento Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies Límite: Child, preschool / Female / Humans / Male / Newborn Idioma: En Revista: Eur J Pediatr Año: 2020 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome de Dificultad Respiratoria del Recién Nacido / Surfactantes Pulmonares / Trastornos del Neurodesarrollo / Trastornos del Crecimiento Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies Límite: Child, preschool / Female / Humans / Male / Newborn Idioma: En Revista: Eur J Pediatr Año: 2020 Tipo del documento: Article País de afiliación: Alemania