Can we improve outcome of congenital diaphragmatic hernia?

Pediatr Surg Int. 2009 Sep;25(9):733-43. doi: 10.1007/s00383-009-2425-8.

Abstract

This review gives an overview of the disease spectrum of congenital diaphragmatic hernia (CDH). Etiological factors, prenatal predictors of survival, new treatment strategies and long-term morbidity are described. Early recognition of problems and improvement of treatment strategies in CDH patients may increase survival and prevent secondary morbidity. Multidisciplinary healthcare is necessary to improve healthcare for CDH patients. Absence of international therapy guidelines, lack of evidence of many therapeutic modalities and the relative low number of CDH patients calls for cooperation between centers with an expertise in the treatment of CDH patients. The international CDH Euro-Consortium is an example of such a collaborative network, which enhances exchange of knowledge, future research and development of treatment protocols.

Publication types

  • Review

MeSH terms

  • Animals
  • Critical Care
  • Extracorporeal Membrane Oxygenation
  • Female
  • Gastroesophageal Reflux / etiology
  • Gastroesophageal Reflux / therapy
  • Hearing Loss, Sensorineural / etiology
  • Hernia, Diaphragmatic / complications*
  • Hernia, Diaphragmatic / etiology
  • Hernias, Diaphragmatic, Congenital*
  • High-Frequency Ventilation
  • Humans
  • Hypoxia, Brain / etiology
  • Infant, Newborn
  • Intestinal Obstruction / etiology
  • Intestinal Obstruction / therapy
  • Language Disorders / etiology
  • Lung Diseases / etiology
  • Lung Diseases / therapy
  • Motor Skills Disorders / etiology
  • Pregnancy
  • Prenatal Care
  • Respiratory Tract Infections / etiology