Obstetrics, Gynaecology and Reproductive Medicine
Volume 18, Issue 10 , Pages 272-278, October 2008

Sickle cell disease in pregnancy

Eugene Oteng-Ntim MBBS PGDip MRCOG is Consultant Obstetrician at the Women's Services, Guys & St Thomas' NHS Foundation Trust, London, UK

Apryll R Chase MBBS DFFP is a Specialist Registrar Obstetrics and Gynaecology at the Women's Services, Guys & St Thomas' NHS Foundation Trust, London, UK

Jo Howard MBBS MRCP is a Consultant Haematologist at the Department of Haematology, Guys & St Thomas' NHS Foundation Trust, London, UK

Nina Khazaezadeh is a Consultant Midwife in Public Health, Guys & St Thomas’ NHS Foundation Trust, London, UK

Elizabeth N Anionwu RN NV Tutor PhD CBE is at the Mary Seacole Centre for Nursing Practice, Thames Valley University, London, UK

Abstract 

With advances in management, the majority of women in the UK with sickle cell disease now survive to have children. The high risk of fetal and maternal sequelae in their pregnancies mandates multidisciplinary management involving an obstetrician, a haematologist, an anaesthetist and a haemoglobinopathy specialist nurse. Hydroxycarbamide, a new treatment for sickle cell disease, is contraindicated in pregnancy. Exchange transfusion may be indicated in women with serious obstetric or haematological complications. In those with sickle cell disease, the entire pregnancy is a high-risk period that warrants close monitoring. It is thus important for every obstetrician to be familiar with the condition.

Keywords: clinical presentation, pregnancy, pathophysiology, sickle cell disease, management

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PII: S1751-7214(08)00158-9

doi:10.1016/j.ogrm.2008.08.001

Obstetrics, Gynaecology and Reproductive Medicine
Volume 18, Issue 10 , Pages 272-278, October 2008