Abstract
Pregnancy in repaired tetralogy of Fallot may be associated with arrhythmia, heart failure and low birthweight babies. Women who have favourable anatomy and underwent uncomplicated repair of tetralogy of Fallot in childhood can expect low risks in pregnancy and good life expectancy. However, higher maternal risk is associated with features such as more complex underlying anatomy and surgical history, residual or postoperative haemodynamically significant lesions and abnormal right or left ventricular function. For selected patients, prepregnancy intervention for the most common lesion, pulmonary regurgitation, may be justified. For women without a family history of congenital heart disease, the risk of vertical transmission is low at around 2-3% unless the patient also has DiGeorge syndrome which will affect 50% of offspring. Elective DiGeorge genetic testing should be offered at precounselling and fetal echocardiography in the antenatal period.
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- CMR:
-
Cardiovascular magnetic resonance
- ECG:
-
Electrocardiogram
- MAPCAs:
-
Major aortopulmonary collateral arteries
- PR:
-
Pulmonary regurgitation
- RA:
-
Right atrium
- RPA:
-
Right pulmonary artery
- RV:
-
Right ventricle
- RVOT:
-
Right ventricular outflow tract
- WHO:
-
World Health Organisation
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Acknowledgements
Sonya V. Babu-Narayan is supported by an Intermediate Clinical Research Fellowship from the British Heart Foundation (FS/11/38/28864). This project was supported by the NIHR Cardiovascular Biomedical Research Unit of Royal Brompton and Harefield NHS Foundation Trust and Imperial College London. This report is an independent research by the National Institute for Health Research Biomedical Research Unit Funding Scheme. The views expressed in this publication are those of the author(s) and not necessarily those of the NHS, the National Institute for Health Research or the Department of Health.
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Babu-Narayan, S.V., Li, W., Uebing, A. (2017). Pregnancy in Repaired Tetralogy of Fallot. In: Roos-Hesselink, J., Johnson, M. (eds) Pregnancy and Congenital Heart Disease. Congenital Heart Disease in Adolescents and Adults. Springer, Cham. https://doi.org/10.1007/978-3-319-38913-4_7
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