Author Of 1 Presentation

INCIDENCE OF ANTENATALLY MISSED MAJOR CONGENITAL HEART DISEASE (CHD) 1, EXPERIENCE FROM A UK TERTIARY NEONATAL UNIT.

Room
Doppler Hall
Date
20.06.2019
Session Time
09:10 - 10:40
Session Name
Duration
10 Minutes

Abstract

Background

Major Congenital Heart Disease (CHD) occurs in about 35/10,000 births.Despite advances in screening programme,up to 50% of major congenital heart diseases were still missed on fetal anomaly scans in UK.

Objectives

To identify missed cases of major congenital heart disease1 which require immediate cardiac assessment and/or treatment within the first two weeks of a child’s life.

Methods

Babies born from 1st January 2014- 31st Dec 2018 who were diagnosed with CHD were identified from local neonatal database. Cases with confirmed post-natal echocardiogram CHD were included and cases identified antenatally were excluded. Isolated cases of ASD and VSD were also excluded from analysis.

Results

48 babies with CHD were identified. 30 were missed on antenatal screening. Of them, 17 had major CHD needing surgical intervention. Out of 17, 11 had major cyanotic heart disease and 6 had major acyanotic heart disease.

Significant CHD –Postnatal diagnosis

S.I no

Cyanotic

Acyanotic

Mixed

1

Tetrology Of Fallot (TOF)

Hypoplastic Left Heart Syndrome

Cardiac TAPVD

2

TOF

COA+ASD

Supracardiac TAPVC

3

Critical Pulmonary stenosis

Interruprted Aortic Arch

TAPVD

4

Pulmonary Atresia

Hypoplastic Left Ventricle

Truncus Arteriosus + VSD

5

Critical Pulmonary Stenosis

Transverse Arch Hypoplasia

Aoto-pulmonary window

6

VSD needing medical/surgical closure

TGA +VSD

Conclusion

Up to 35% of major congenital heart diseases were still missed on foetal anomaly scans in UK. This highlights importance of implementing newborn pulse oximetry screening in conjunction with Foetal Cardiac Screening Protocol to improve detection of major CHD.

References:

NHS Fetal Anomaly Screening Programme - Congenital Heart Disease. Version 2. Apr 2013.

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