Terminating Routine Cord Blood RhD Typing of the Newborns to Guide Postnatal Anti-D Immunoglobulin Prophylaxis Based on the Results of Fetal RHD Genotyping.


Journal

Fetal diagnosis and therapy
ISSN: 1421-9964
Titre abrégé: Fetal Diagn Ther
Pays: Switzerland
ID NLM: 9107463

Informations de publication

Date de publication:
2023
Historique:
received: 14 03 2023
accepted: 09 06 2023
medline: 4 10 2023
pubmed: 29 6 2023
entrez: 28 6 2023
Statut: ppublish

Résumé

Targeted routine antenatal prophylaxis with anti-D immunoglobulin (Ig) only to RhD-negative pregnant women who carry RhD-positive fetuses (determined by fetal RHD genotyping) has reduced D-alloimmunization significantly when administered in addition to postnatal prophylaxis. Achieving high analysis sensitivity and few false-negative fetal RHD results will make RhD typing of the newborn redundant. Postnatal prophylaxis can then be given based on the result of fetal RHD genotyping. Terminating routine RhD typing of the newborns in cord blood will streamline maternity care. Accordingly, we compared the results of fetal RHD genotyping with RhD typing of the newborns. Fetal RHD genotyping was performed, and antenatal anti-D Ig was administered at gestational week 24 and 28, respectively. Data for 2017-2020 are reported. Ten laboratories reported 18,536 fetal RHD genotypings, and 16,378 RhD typing results of newborns. We found 46 false-positive (0.28%) and seven false-negative (0.04%) results. Sensitivity of the assays was 99.93%, while specificity was 99.24%. Few false-negative results support the good analysis quality of fetal RHD genotyping. Routine cord blood RhD typing will therefore be discontinued nationwide and postnatal anti-D Ig will now be given based on the result of fetal RHD genotyping.

Identifiants

pubmed: 37379821
pii: 000531694
doi: 10.1159/000531694
pmc: PMC10614222
doi:

Substances chimiques

RHO(D) antibody 0
Rh-Hr Blood-Group System 0
Rho(D) Immune Globulin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

276-281

Informations de copyright

© 2023 The Author(s). Published by S. Karger AG, Basel.

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Auteurs

Monica Stensrud (M)

Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway.

Mette Silihagen Bævre (MS)

Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway.

Inger Margit Alm (IM)

Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway.

Ho Yi Wong (HY)

Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway.

Ida Herud (I)

Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway.

Barbora Jacobsen (B)

Department of Immunology and Transfusion Medicine, St. Olavs University Hospital, Trondheim, Norway.

Dijanne Dicky Jannie Anne de Vos (DDJA)

Department of Laboratory Medicine, Blood Bank, Nordland Hospital, Bodø, Norway.

Helena Eriksson Stjern (HE)

Department of Immunology and Transfusion Medicine, Akershus University Hospital, Lørenskog, Norway.

Ingvild Hausberg Sørvoll (IH)

Department of Laboratory Medicine, University Hospital of North Norway, Tromsø, Norway.

Janne Brit Barane (JB)

Department of Immunology and Transfusion Medicine, Stavanger University Hospital, Stavanger, Norway.

Tonje Espeland Bagås (TE)

Department of Immunology and Transfusion Medicine, Haukeland University Hospital, Bergen, Norway.

Mona Rasmussen (M)

Innlandet Hospital Trust, Lillehammer, Norway.

Norunn Ulvahaug (N)

Transfusion Service, Vestfold Hospital, Tønsberg, Norway.

Vendula Wamstad (V)

Department of Laboratory Medicine, Vestre Viken Health Trust, Drammen, Norway.

Geir Tomter (G)

Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway.

Cigdem Akalin Akkök (CA)

Department of Immunology and Transfusion Medicine, Oslo University Hospital, Oslo, Norway.

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Classifications MeSH