[Prognostic factors and survival in neonates with congenital diaphragmatic hernia]

Luis R Longo dos Santos1, João G Maksoud-Filho, Uenis Tannuri

  • 1Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo (USP), São Paulo, SP, Brazil. luisrls@icr.hcnet.usp.br

Jornal De Pediatria
|September 16, 2003
PubMed

Insights

Congenital diaphragmatic hernia (CDH) survival in newborns is 56%, with severe respiratory distress and hypoxemia predicting poor outcomes. Extracorporeal membrane oxygenation may improve survival for non-responsive cases.

Area of Science:

  • Pediatric Surgery
  • Neonatology
  • Medical Research

Background:

  • Congenital diaphragmatic hernia (CDH) is a serious condition affecting newborns.
  • Accurate prognostic factors are crucial for managing CDH and counseling families.
  • Previous studies highlight the need for updated survival data and treatment strategies.

Purpose of the Study:

  • To determine prognostic factors for neonatal survival in congenital diaphragmatic hernia (CDH) patients.
  • To compare survival outcomes with international medical literature.
  • To inform clinical management and family counseling regarding CDH.

Main Methods:

  • A retrospective study of 27 newborns with congenital diaphragmatic hernia (CDH) was conducted.
  • Data were collected from April 1991 to January 2002 at a major university hospital.
  • Statistical comparisons were made with existing medical literature meta-analysis data.

Main Results:

  • Overall neonatal survival for CDH was 56% (15/27).
  • Severe respiratory distress, early mechanical ventilation, and severe hypoxemia were significant predictors of poor outcomes.
  • Survival rates differed between infants born at the institution (33%) and transferred infants (73%).

Conclusions:

  • The high mortality rate for congenital diaphragmatic hernia (CDH) in this study aligns with international findings.
  • Extracorporeal membrane oxygenation (ECMO) may reduce mortality in refractory CDH cases.
  • Family counseling for CDH can be guided by current global medical literature standards.
Abstract

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