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Congenital Diaphragmatic Hernia
Congenital Diaphragmatic Hernia
Congenital Diaphragmatic Hernia
DIAPHRAGMATIC HERNIA
GROUP: IM-650
Congenital diaphragmatic hernia (CDH) occurs when there is a hole in the diaphragm,
which is the the thin sheet of muscle seperating the chest from the abdomen.
When this gap forms during a fetus’s development in the womb, the bowel, stomach
or even the liver can move into the chest cavity.
It is associated with pulmonary hypoplasia.
CHD occurs in 1 in every 2500
births. It is 80 % left sided.
CHD
Etiology
Typically can be diagnosed at prenatal stage with the use of USG (40-60 %). It can be
diagnosed typically around 21-24 weeks of gestation.
Classic triad- cyanosis, dyspnea, apparent dextrocardia
Scaphoid abdomen
Bulging chest
Variable presentation
Amniocentesis
Congenital Diaphragmatic Hernia
Diagnosis Cont’d
After birth :
A chest xray nasogastric tube in situ is needed to confirm the diagnosis
CHD Cont’d
Management of CHD
Before birth :
Antenatally diagnosed case should be delivered in well equipped hospital
Termination of pregnancy may required in some cases diagnosed with chromosomal
anomalies
Fetal surgeries
Tracheal balloon obstruction
Maternal corticosteroids
Congenital Diaphragmatic Hernia
Management of CHD
After birth :
Initial mgt : Careful protocols of respiratory assistance should be implemented.
(Prolonged BVM should be avoided) (immediate intubation-low volume, low PIP, and
high frequency ventilation)
Ventilation strategies : ECMO (Extracorporeal membrane oxygenation)