Document Detail


Congenital diaphragmatic hernia.
MedLine Citation:
PMID:  18005901     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The incidence of congenital diaphragmatic hernia (CDH) may be as high as 1 in 2000. Over the past two decades, antenatal diagnosis rates have increased, the pathophysiology of CDH has become better understood, and advances in clinical care, including foetal surgery, have occurred. However, there remains a paucity of randomised controlled trials to provide evidence-based management guidelines. Reports of improved survival rates appear to be confined to a select subset of CDH infants, surviving to surgical repair, while the overall mortality, at over 60%, appears to be unchanged, largely due to the often forgotten 'hidden mortality' of CDH. The significant long-term morbidity in surviving infants has become apparent, and the need for long-term multidisciplinary follow up established. A total of 10% of cases may present later in life, and misdiagnosis on initial chest X-ray may lead to significant morbidity.
Authors:
Paul D Robinson; Dominic A Fitzgerald
Publication Detail:
Type:  Journal Article; Review     Date:  2007-11-05
Journal Detail:
Title:  Paediatric respiratory reviews     Volume:  8     ISSN:  1526-0542     ISO Abbreviation:  Paediatr Respir Rev     Publication Date:  2007 Dec 
Date Detail:
Created Date:  2007-11-16     Completed Date:  2008-03-05     Revised Date:  2009-10-14    
Medline Journal Info:
Nlm Unique ID:  100898941     Medline TA:  Paediatr Respir Rev     Country:  England    
Other Details:
Languages:  eng     Pagination:  323-34; quiz 334-5     Citation Subset:  IM    
Affiliation:
Department of Respiratory Medicine, The Children's Hospital at Westmead, University of Sydney, New South Wales, Westmead, Australia. paulr3@chw.edu.au
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MeSH Terms
Descriptor/Qualifier:
Child
Extracorporeal Membrane Oxygenation
Fetal Diseases / diagnosis
Hernia, Diaphragmatic / complications,  congenital*,  physiopathology
Humans
Prenatal Diagnosis
Prognosis
Respiratory Insufficiency / etiology

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