The Obstetrician & Gynaecologist 2008;10:1:33-37
doi: 10.1576/toag.10.1.033.27375
Copyright © 2008 by the Royal College of Obstetricians and Gynaecologists.
Congenital abnormalities: failure to detect and treat
Pamela Loughna, MD MRCGP FRCOG, Senior Lecturer in Obstetrics/Honorary Consultant Obstetrician1
1. Academic Division of Obstetrics and Gynaecology, Nottingham City Hospital, Hucknall Road, Nottingham NG5 1PB, UK Email: pam.loughna{at}nottingham.ac.uk (corresponding author)
Key content:
- Not all congenital abnormalities can be detected by routine screening.
- The primary reason for litigation in this area is failure to offer termination of pregnancy as a result of failure to diagnose a problem.
Learning objectives:
- To be aware that prenatal screening for anomalies is not restricted to screening for trisomy 21.
- To be aware of the limitations of the current UK screening programme.
- To be aware that difficulties encountered in achieving a satisfactory screening test must be recorded and the mother informed.
Ethical issues:
- Prenatal diagnosis is not a seek-and-destroy mission.
- Optimum management may, however, include termination of pregnancy.
Please cite this article as: Loughna P. Congenital abnormalities: failure to detect and treat. The Obstetrician & Gynaecologist 2008;10:33–37.
Keywords congenital abnormality / medicolegal / trisomy 21 / UK National Screening Committee / ultrasound scanning
Copyright © 2008 by the Royal College of Obstetricians and Gynaecologists.