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Disease severity in subsequent pregnancies with RhD immunization: A nationwide cohort.
Zwiers, Carolien; Slootweg, Yolentha M; Koelewijn, Joke M; Ligthart, Peter C; van der Bom, Johanna G; van Kamp, Inge L; Lopriore, Enrico; van der Schoot, C Ellen; Oepkes, Dick; de Haas, Masja.
Afiliação
  • Zwiers C; Department of Obstetrics, Leiden University Medical Center, Leiden, the Netherlands.
  • Slootweg YM; Department of Experimental Immunohematology, Sanquin Research and Landsteiner Laboratory, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
  • Koelewijn JM; Department of Obstetrics, Leiden University Medical Center, Leiden, the Netherlands.
  • Ligthart PC; Department of Experimental Immunohematology, Sanquin Research and Landsteiner Laboratory, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
  • van der Bom JG; Department of Immunohematology, Sanquin Diagnostic Services, Amsterdam, the Netherlands.
  • van Kamp IL; Department of Immunohematology, Sanquin Diagnostic Services, Amsterdam, the Netherlands.
  • Lopriore E; Center for Clinical Transfusion Research, Sanquin Research, Leiden, the Netherlands.
  • van der Schoot CE; Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, the Netherlands.
  • Oepkes D; Department of Obstetrics, Leiden University Medical Center, Leiden, the Netherlands.
  • de Haas M; Department of Pediatrics, Leiden University Medical Center, Leiden, the Netherlands.
Vox Sang ; 119(8): 859-866, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38772910
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. 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).

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 (p < 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%).

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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistema do Grupo Sanguíneo Rh-Hr / Eritroblastose Fetal Limite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistema do Grupo Sanguíneo Rh-Hr / Eritroblastose Fetal Limite: Adult / Female / Humans / Newborn / Pregnancy Idioma: En Ano de publicação: 2024 Tipo de documento: Article