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[Congenital diaphragmatic hernia presenting after the neonatal period]

A Szold1, D Dror, R Udassin

  • 1Dept. of Pediatric Surgery, Hadassah-University Hospital, Jerusalem.

Harefuah
|April 1, 1990
PubMed

Insights

Congenital diaphragmatic hernia (Bochdalek) is a rare birth defect. Early diagnosis and surgery, even in older children, improve outcomes for this condition.

Area of Science:

  • Pediatric Surgery
  • Congenital Malformations
  • Neonatal Care

Context:

  • Congenital diaphragmatic hernia (Bochdalek) is a significant congenital malformation with high neonatal mortality.
  • Diagnosis after the neonatal period is uncommon, but prognosis is generally favorable.
  • This study focuses on surgical outcomes in children diagnosed beyond the neonatal stage.

Purpose:

  • To evaluate the surgical outcomes of congenital diaphragmatic hernia (Bochdalek) in children diagnosed after the neonatal period.
  • To assess the impact of early surgical intervention on prognosis in this patient group.

Summary:

  • Eleven children aged 6 months to 5.5 years with congenital diaphragmatic hernia (Bochdalek) were surgically treated.
  • Nine patients presenting with respiratory symptoms underwent semi-elective surgery with excellent results.
  • Two patients who presented with strangulation of incarcerated bowel died, highlighting the risk of delayed diagnosis and treatment.

Impact:

  • Early diagnosis and surgical intervention are crucial for improving survival rates in congenital diaphragmatic hernia (Bochdalek).
  • Even asymptomatic cases benefit from early surgery, as demonstrated by the favorable outcomes in the majority of patients.
  • This research underscores the importance of considering congenital diaphragmatic hernia (Bochdalek) in older children presenting with respiratory issues or bowel obstruction.

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