Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-09T06:47:29.658Z Has data issue: false hasContentIssue false

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

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)