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Disease severity in subsequent pregnancies with RhD immunization: A nationwide cohort.

Authors :
Zwiers C
Slootweg YM
Koelewijn JM
Ligthart PC
van der Bom JG
van Kamp IL
Lopriore E
van der Schoot CE
Oepkes D
de Haas M
Source :
Vox sanguinis [Vox Sang] 2024 Aug; Vol. 119 (8), pp. 859-866. Date of Electronic Publication: 2024 May 21.
Publication Year :
2024

Abstract

Background and Objectives: To evaluate the severity of haemolytic disease of the foetus and newborn (HDFN) in subsequent pregnancies with RhD immunization and to identify predictive factors for severe disease.<br />Materials and Methods: Nationwide prospective cohort study, including all pregnant women with RhD antibodies. All women with at least two pregnancies with RhD antibodies and RhD-positive foetuses were selected. The main outcome measure was the severity of HDFN in the first and subsequent pregnancy at risk. A subgroup analysis was performed for the group of women where RhD antibodies developed after giving birth to an RhD-positive child and thus after receiving anti-D at least twice (group A) or during the first pregnancy at risk for immunization (group B).<br />Results: Sixty-two RhD immunized women with a total of 150 RhD-positive children were included. The severity of HDFN increased for the whole group significantly in the subsequent pregnancy (pā€‰<ā€‰0.001), although it remained equal or even decreased in 44% of women. When antibodies were already detected at first trimester screening in the first immunized pregnancy, after giving birth to an RhD-positive child (group A), severe HDFN in the next pregnancy was uncommon (22%). Especially when no therapy or only non-intensive phototherapy was indicated during the first immunized pregnancy (6%) or if the antibody-dependent cell-mediated cytotoxicity result remained <10%. Contrarily, women with a negative first trimester screening and RhD antibodies detected later during the first pregnancy of an RhD-positive child (group B), often before they had ever received anti-D prophylaxis, were most prone for severe disease in a subsequent pregnancy (48%).<br />Conclusion: RhD-mediated HDFN in a subsequent pregnancy is generally more severe than in the first pregnancy at risk and can be estimated using moment of antibody detection and severity in the first immunized pregnancy. Women developing antibodies in their first pregnancy of an RhD-positive child are at highest risk of severe disease in the next pregnancy.<br /> (© 2024 The Authors. Vox Sanguinis published by John Wiley & Sons Ltd on behalf of International Society of Blood Transfusion.)

Details

Language :
English
ISSN :
1423-0410
Volume :
119
Issue :
8
Database :
MEDLINE
Journal :
Vox sanguinis
Publication Type :
Academic Journal
Accession number :
38772910
Full Text :
https://doi.org/10.1111/vox.13651