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Screening for congenital heart disease

Published online by Cambridge University Press:  01 May 1999

S Hunter
Affiliation:
Department of Academic Cardiology, Freeman Hospital, Newcastle upon Tyne
J Norman
Affiliation:
Department of Obstetrics and Gynaecology, Royal Victoria Infirmary, Newcastle upon Tyne

Abstract

Congenital heart disease (CHD) is the commonest congenital malformation with an incidence of approximately 8 per 1000 live births. Half of the defects are severe. Cardiac anomalies at birth are 4 times more common than neural tube defects and 6.5 times more common than chromosomal abnormalities. Within a stillborn population the incidence is approximately 10 times that of live births. Congenital heart disease is responsible for approximately 40% of the perinatal and 60% of post neonatal deaths due to congenital anomalies. Despite screening of the infant population, 30% of cases of CHD are unsuspected or unconfirmed prior to death. Sadly, many of these missed lesions are correctable. However, the overall outlook for CHD is excellent since 85% of infants born with heart malformations will survive into adult life.

Type
Research Article
Copyright
© 1999 Cambridge University Press

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