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Early perfluorodecalin lung distension in infants with congenital diaphragmatic hernia

G M Walker1, K F Kasem, S J O'Toole

  • 1Department of Surgical Paediatrics, Royal Hospital for Sick Children, Yorkhill NHS Trust, Glasgow, Scotland.

Insights

Perfluorodecalin lung distension in infants with severe congenital diaphragmatic hernia (CDH) on ECMO support significantly increased lung size. This approach shows promising outcomes for neonates with CDH, potentially promoting lung growth.

Area of Science:

  • Neonatal Medicine
  • Pediatric Surgery
  • Pulmonary Medicine

Background:

  • Pulmonary hypoplasia is a major cause of mortality in infants with severe congenital diaphragmatic hernia (CDH).
  • Accelerated postnatal lung growth has been observed in animal models using perfluorocarbon lung distension.
  • This study investigates perfluorodecalin lung distension in neonates with severe CDH requiring extracorporeal membrane oxygenation (ECMO) support.

Purpose of the Study:

  • To measure the effects of perfluorodecalin lung distension on lung volume in neonates with severe CDH on ECMO.
  • To assess the radiographic changes and clinical outcomes associated with this intervention.

Main Methods:

  • Six neonates with severe CDH requiring ECMO were treated with perfluorodecalin lung instillation and continuous positive airway pressure for a mean of 7.7 days.
  • Perfluorodecalin was exchanged four times daily.
  • Lung volume was estimated from radiographic projections using the ECMO cannula as a reference.

Main Results:

  • Perfluorodecalin instillation began shortly after ECMO initiation (mean 13.5 hours).
  • A significant increase in lung volume was observed (affected lung: 272% increase; contralateral lung: 51% increase; P <.02 for both).
  • All six patients survived and underwent CDH repair on ECMO.

Conclusions:

  • Early perfluorodecalin lung distension in severe CDH neonates on ECMO leads to significant radiographic lung enlargement.
  • Clinical outcomes are encouraging, with all patients surviving.
  • Potential mechanisms include alveolar recruitment, dilatation, and accelerated postnatal lung growth.
Abstract

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