Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Jul 1;11(1):e2019040.
doi: 10.4084/MJHID.2019.040. eCollection 2019.

Sickle Cell Disease and Pregnancy

Affiliations
Review

Sickle Cell Disease and Pregnancy

Dipty Jain et al. Mediterr J Hematol Infect Dis. .

Abstract

Sickle cell disease (SCD) is the most common inherited hemoglobinopathy and is associated with increased risk of complications and early mortality. Nowadays, with improved health care facilities, antibiotic prophylaxis, vaccination, and availability of drugs like hydroxyurea, the life expectancy of SCD patients has improved. More women are reaching reproductive age group and are expressing their desire to reproduce. Though SCD adversely affects pregnancy, leading to increased incidence of maternal and perinatal complications like pre-eclampsia, preterm labor, IUGR, abortions etc., adequate care throughout pregnancy ensures a better outcome. Also, recent advancements in the fields of prenatal diagnosis and preimplantation genetic diagnosis, help couples suffering from SCD to have a healthy baby. This paper focuses on the effects of SCD on pregnancy outcomes and effective management of complications during pregnancy, also comparing maternal and perinatal outcomes in studies conducted in different countries. The second part of the paper summarizes pregnancy management in SCD for better maternal and fetal outcomes.

Keywords: Pregnancy; Sickle Cell Disease.

PubMed Disclaimer

Conflict of interest statement

Competing interests: The authors have declared that no competing interests exist.

Similar articles

Cited by

References

    1. Piel FB, Hay SI, Gupta S, Weatherall DJ, Williams TN. Global burden of sickle cell anaemia in children under five, 2010–2050: modelling based on demographics, excess mortality, and interventions. Plos Med. 2013;10(7):e1001484. doi: 10.1371/journal.pmed.1001484. - DOI - PMC - PubMed
    1. Koshy M. Sickle cell disease and pregnancy. Blood Rev. 1995;9(3):157–64. doi: 10.1016/0268-960X(95)90021-7. - DOI - PubMed
    1. Rogers DT, Molokie R. Sickle cell disease in pregnancy. Obstetrics and Gynecology Clinics of North America. 2010;37(2):223–237. doi: 10.1016/j.ogc.2010.02.015. [pubmed: 20685550] - DOI - PubMed
    1. Luban NL, Leikin SL, August GA. Growth and development in sickle cell anemia. Preliminary report. Am J Pediatr Hematol Oncol. 1982;4:61–65. - PubMed
    1. Jesus AC, Konstantyner T, Lôbo IK, Braga JA. Socioeconomic and nutritional characteristics of children and adolescents with sickle cell anemia: a systematic review. Revistapaulista de Pediatria. 2018 Dec;36(4):491–9. doi: 10.1590/1984-0462/;2018;36;4;00010. - DOI - PMC - PubMed