Growth and development after oesophageal atresia surgery: Need for long-term multidisciplinary follow-up

Hanneke IJsselstijn1, Saskia J Gischler1, Leontien Toussaint1

  • 1Department of Intensive Care and Paediatric Surgery, Erasmus MC - Sophia Children's Hospital, Rotterdam, The Netherlands.

Insights

Long-term survival for oesophageal atresia patients exceeds 90%. However, growth and neurodevelopmental issues are common, necessitating multidisciplinary adult care to enhance quality of life.

Area of Science:

  • Pediatric Surgery
  • Developmental Pediatrics
  • Longitudinal Health Outcomes

Background:

  • Oesophageal atresia (OA) survival rates now exceed 90%.
  • Long-term follow-up has evolved from surgical/gastrointestinal focus to a multidisciplinary approach.
  • Focus is shifting to long-term morbidity, particularly growth and neurodevelopment.

Purpose of the Study:

  • To review the literature on long-term morbidity in oesophageal atresia patients.
  • To discuss physical growth and neurodevelopmental outcomes.
  • To propose a multidisciplinary follow-up schedule into adulthood.

Main Methods:

  • Literature review of long-term morbidity in oesophageal atresia patients.
  • Analysis of studies focusing on physical growth (stunting, wasting).
  • Review of neurodevelopmental outcomes beyond preschool age.

Main Results:

  • Growth problems like stunting and wasting are frequent in OA patients.
  • Sufficient longitudinal data on catch-up growth into adulthood is lacking.
  • OA patients are at risk for academic and motor function delays, with limited data beyond preschool age.

Conclusions:

  • Growth retardation determinants in OA patients require further investigation.
  • Long-term neurodevelopmental studies are scarce but indicate potential academic and motor issues.
  • A multidisciplinary follow-up into adulthood is crucial for improving OA patient quality of life.

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