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Chapter 5 - Prenatal Diagnosis, Screening and Wrongful Birth

Published online by Cambridge University Press:  22 April 2022

By
David Howe
Edited by
Swati Jha  and
Eloise Power
Swati Jha
Affiliation:
Royal Hallamshire Hospital, Sheffield
Eloise Power
Affiliation:
Sergeants’ Inn, London
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Summary

The claimant had a baby with Down’s syndrome in her first pregnancy. It was stated by the claimant that two opportunities to carry out screening for Down’s syndrome were missed, and that had this been offered and detected the underlying abnormality, it would have led to a termination of the pregnancy.

Type
Chapter
Information
Lessons from Medicolegal Cases in Obstetrics and Gynaecology
Improving Clinical Practice
 , pp. 55 - 68
Publisher: Cambridge University Press
Print publication year: 2022

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References

Fetal Anomaly Screening Programme. Fetal Anomaly Screening Programme Handbook for Ultrasound Practitioners. Published 2015.Google Scholar
Fetal Anomaly Screening Programme. NHS Fetal Anomaly Screening Programme Handbook. Published 2018.Google Scholar
National Down’s Syndrome Screening Programme for England. Antenatal Screening – Working Standards for Down’s Syndrome Screening. Published 2007.Google Scholar
Callen, PW, et al. Columns of the fornix, not to be mistaken for the cavum septi pellucidi on prenatal sonography. J Ultrasound Med 2008; 27(1): 25–31.Google Scholar
Guibaud, L. Fetal cerebral ventricular measurement and ventriculomegaly: time for procedure standardization. Ultrasound Obstet Gynecol 2009; 34(2): 127–30.CrossRefGoogle ScholarPubMed
Salomon, LJ, et al. Practice guidelines for performance of the routine mid-trimester fetal ultrasound scan. Ultrasound Obstet Gynecol 2011; 37(1): 116–26.Google Scholar
Carvalho, J, et al. ISUOG Practice Guidelines (updated): sonographic screening examination of the fetal heart. Ultrasound Obstet Gynecol 2013; 41(3): 348–59.CrossRefGoogle Scholar

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