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RhD alloimmunization in pregnancy and hemolytic disease of the fetus and newborn in Africa: A systematic review and meta-analysis

  • Assefa Desalew
  • , Rafiki Nickson Mjema
  • , Henk Schonewille
  • , C. Ellen van der Schoot
  • , Derek P. de Winter
  • , Thomas van den Akker
  • , Tadesse Gure
  • , Jeremia Pyuza
  • , Abera Kenay Tura
  • , E. J.T.Joanne Verweij
  • , Enrico Lopriore
  • , Tienke Vermeiden
  • , Peter Ligthart
  • , Tewodros Tesfa
  • , Konjit Eshetu
  • , Priscus John Mapendo
  • , Jeremiah John Hhera
  • , Bariki Mchome
  • , Patricia Swai
  • , Blandina T. Mmbaga
  • Aisa Shayo, Peter Moons, Kondwani Kawaza, Luis Gadama, Gari Makonyola
  • Haramaya University
  • Leiden University
  • Kilimanjaro Christian Medical Centre
  • University of Amsterdam
  • Sanquin Blood Supply Foundation
  • Kamuzu University of Health Sciences
  • Queen Elizabeth Central Hospital Malawi

Research output: Contribution to journalReview articlepeer-review

1 Citation (Scopus)

Abstract

Although hemolytic disease of the fetus and newborn (HDFN), caused by maternal alloimmunization against fetal erythrocytes, has been nearly eliminated in high-income settings, it likely remains a significant public health problem in low-resource settings in Africa and elsewhere. We performed a comprehensive literature review across six major databases to determine the proportion of RhD-negativity, anti-D immunoprophylaxis utilization, RhD-alloimmunization prevalence, and the burden of RhD-mediated HDFN among pregnant women in Africa. A random-effects model was used to determine pooled estimates. We included 74 studies from 17 countries (42 from Nigeria), published between 1960 and 2024, involving 245,046 pregnancies, mostly from tertiary centers. The proportion of RhD negativity was 4.8 % (95 % CI: 4.1–5.7 %). The proven RhD alloimmunization rate was 5.8 % (95 % CI: 4.1–8.2 %). In multigravida women, the proportion of RhD alloimmunization was 5.7 % (95 % CI: 3.1–10.4 %). Anti-D immunoprophylaxis utilization after a previous pregnancy, reported in 18 studies (1490/3756 women), was 29.7 % (95 % CI: 18.0–45.0 %), with no effect on alloimmunization rate. Nine studies (including 50 neonates from 168 alloimmunized women) provided data on HDFN, with a pooled prevalence of 36.2 % (95 % CI: 16.8–61.4 %). In many papers, the specificity of the alloantibodies was not determined. Data on gravidity and the clinical definition of HDFN were incomplete. We conclude that there is a lack of robust data from Africa, thereby hampering HDFN prevention efforts. To eliminate HDFN in Africa, integrated strategies are urgently needed, including universal RhD typing and antibody screening, access to polyclonal anti-D immunoprophylaxis, and population-based surveillance.

Original languageEnglish
Article number102700
JournalBest Practice and Research: Clinical Obstetrics and Gynaecology
Volume104
Early online date16 Dec 2025
DOIs
Publication statusPublished - Feb 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Africa
  • anti-D immunoprophylaxis
  • Erythroblastosis
  • Fetal
  • Hemolytic disease of fetus and newborn
  • Pregnancy
  • Rh disease
  • RhD-alloimmunization

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