Position statement on the management of pregnancy in sickle cell disease

Aust N Z J Obstet Gynaecol. 2024 Sep 27. doi: 10.1111/ajo.13888. Online ahead of print.

Abstract

Sickle cell disease (SCD) is a hereditary haemoglobinopathy which causes multi-organ dysfunction. Pregnancies in SCD are high risk with significant maternal and fetal morbidity and mortality, including vaso-occlusive crises, thrombosis, anaemia, placental insufficiency, fetal growth restriction, preterm birth and medication effects. High level evidence on this topic is lacking. The Australian Sickle Cell Disease Working Group has reviewed international guidelines on this topic and provide an up-to-date and structured approach to the pre-conception, antenatal, birth and post-partum management of these women. Early and comprehensive multidisciplinary care involving experienced clinicians is recommended.

Keywords: anaemia; pregnancy; pregnancy complications; prenatal care; sickle cell.