[Per and post-natal medical management of congenital diaphragmatic hernia]. / Prise en charge médicale per et post-natale de la hernie congénitale du diaphragme.
Arch Pediatr
; 17 Suppl 3: S85-92, 2010 Sep.
Article
in Fr
| MEDLINE
| ID: mdl-20728814
ABSTRACT
Congenital diaphragmatic hernia (CDH) is a 1 out of 3500 live-born malformation with persistent 30-40% mortality rate, related to severe pulmonary hypoplasia and hypertension. Better knowledge on the mechanisms inducing failure of adaptation at birth is a prerequisite for improving CDH prognosis. CDH is also associated with longterm morbidity, including prolonged respiratory failure, failure to growth, oral aversion, and scoliosis. Early prevention starting as soon as the first hours of life are required to reduced long term morbidity. The aims of the management are not only to reduce early mortality, related to persistent pulmonary hypertension, but also to prevent late morbidity.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Hernias, Diaphragmatic, Congenital
/
Infant, Newborn, Diseases
Type of study:
Etiology_studies
Limits:
Humans
/
Newborn
Language:
Fr
Journal:
Arch Pediatr
Year:
2010
Document type:
Article