Abstract Survival rates in oesophageal atresia patients have reached over 90%. In long-term follow-up studies the focus has shifted from purely surgical or gastrointestinal evaluation to a multidisciplinary approach. We reviewed the literature on the long-term morbidity of these patients and discuss mainly issues of physical growth and neurodevelopment. We conclude that growth problems–both stunting and wasting–are frequently seen, but that sufficient longitudinal data are lacking. Therefore, it is unclear whether catch-up growth into adolescence and adulthood occurs. Data on determinants of growth retardation are also lacking in current literature. Studies on neurodevelopment beyond preschool age are scarce but oesophageal atresia pati...
Item does not contain fulltextSurvival rates in esophageal atresia (EA) patients have reached 90%. I...
International audienceBackground data: EA is the most frequent congenital esophageal malformation. L...
AbstractBackground/purposeTo evaluate growth and development in children with anorectal malformation...
markdownabstractAbstract Survival rates in oesophageal atresia patients have reached over 90%. I...
The aim of the study was to analyse the outcomes of children born with oesophageal atresia over the ...
A study carried out at the Paediatric Surgery Units in Siena and Toulouse evaluated the long term fo...
As survival of gastroschisis patients has improved significantly, it has become apparent that longit...
Introduction: Despite proper surgical management in neonatal period, congenital oesophageal atresia ...
Introduction Surgical treatment of esophageal atresia (EA) has markedly improved, allowing the focus...
INTRODUCTION: Long term outcomes of esophageal atresia (OA) are poorly understood. The Federation of...
Treatment modalities for newborns with anatomical congenital anomalies have greatly improved over th...
Background: Adults with esophageal atresia (EA) require a multidisciplinary follow-up approach, taki...
PURPOSE: Treatment for esophageal atresia has advanced over several decades due to improvements in s...
Introduction Gastric transposition (GT) is currently the oesophageal replacement of choice for long...
textabstractSurvival rates in esophageal atresia (EA) patients have reached 90%. In long-term follow...
Item does not contain fulltextSurvival rates in esophageal atresia (EA) patients have reached 90%. I...
International audienceBackground data: EA is the most frequent congenital esophageal malformation. L...
AbstractBackground/purposeTo evaluate growth and development in children with anorectal malformation...
markdownabstractAbstract Survival rates in oesophageal atresia patients have reached over 90%. I...
The aim of the study was to analyse the outcomes of children born with oesophageal atresia over the ...
A study carried out at the Paediatric Surgery Units in Siena and Toulouse evaluated the long term fo...
As survival of gastroschisis patients has improved significantly, it has become apparent that longit...
Introduction: Despite proper surgical management in neonatal period, congenital oesophageal atresia ...
Introduction Surgical treatment of esophageal atresia (EA) has markedly improved, allowing the focus...
INTRODUCTION: Long term outcomes of esophageal atresia (OA) are poorly understood. The Federation of...
Treatment modalities for newborns with anatomical congenital anomalies have greatly improved over th...
Background: Adults with esophageal atresia (EA) require a multidisciplinary follow-up approach, taki...
PURPOSE: Treatment for esophageal atresia has advanced over several decades due to improvements in s...
Introduction Gastric transposition (GT) is currently the oesophageal replacement of choice for long...
textabstractSurvival rates in esophageal atresia (EA) patients have reached 90%. In long-term follow...
Item does not contain fulltextSurvival rates in esophageal atresia (EA) patients have reached 90%. I...
International audienceBackground data: EA is the most frequent congenital esophageal malformation. L...
AbstractBackground/purposeTo evaluate growth and development in children with anorectal malformation...