Evidence map›Paper›PMID 40792190›Full record

ArticleAJOG global reports2025

Clinical characteristics and outcomes of pregnancies at-risk of hemolytic disease of the fetus and newborn in Sweden, Finland, and Denmark: a population-based register study.

Kelvin H M Kwok, Mika Gissler, Mette Ø Thunbo, Elizabeth C Hsia, May Lee Tjoa, Shengxin Liu, Malin Almgren, Vedran Stefanovic, Lars H Pedersen, Agneta Wikman

Abstract read
In one paragraph

Article in AJOG global reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Kelvin H M KwokSchain Research AB, Stockholm, Sweden (Kwok, Liu, and Almgren).
Mika GisslerDepartment of Data and Analytics, Finnish Institute for Health and Welfare, Helsinki, Finland (Gissler).
Mette Ø ThunboDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark (Thunbo and Pedersen).
Elizabeth C HsiaJohnson & Johnson, Spring House, PA (Hsia).
May Lee TjoaJohnson & Johnson, Cambridge, MA (Tjoa).
Shengxin LiuSchain Research AB, Stockholm, Sweden (Kwok, Liu, and Almgren).
Malin AlmgrenSchain Research AB, Stockholm, Sweden (Kwok, Liu, and Almgren).
Vedran StefanovicFetomaternal Medical Centre, Department of Obstetrics and Gynecology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland (Stefanovic).
Lars H PedersenDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark (Thunbo and Pedersen).
Agneta WikmanClinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden (Wikman).

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Red blood cell (RBC) alloimmunization is an immune response where the maternal immune system produces antibodies against fetal RBCs, which can lead to hemolytic disease of the fetus and newborn (HDFN). Despite the significant clinical burden of HDFN, there are few large international cohorts that focus on perinatal care and outcomes of at-risk pregnancies. Objective: To describe the maternal characteristics and outcomes of pregnancies affected by RBC alloimmunization, as well as the characteristics and outcomes of neonates from such pregnancies. Study Design: Utilizing data from nationwide health registers, this population-based cohort study identified all singleton pregnancies in individuals who had ≥1 pregnancy monitored or treated for potential alloimmunization, or ≥1 child with a postnatal diagnosis of HDFN-related conditions, between January 1, 2000, and December 31, 2021, in Sweden and Finland, and between January 1, 1997, and December 31, 2018, in Denmark. Among the identified pregnancies, those with a diagnosis of maternal care for alloimmunization or fetal hydrops, or neonates with a postnatal diagnosis of HDFN-related conditions, were categorized as HDFN pregnancies. The remaining pregnancies-sibling pregnancies that may have been at risk of alloimmunization but did not receive any alloimmunization- or HDFN-related diagnosis-were categorized as non-HDFN pregnancies. Results: This study included 14,732 singleton pregnancies in Sweden, 5863 in Finland, and 11,964 in Denmark. Among these pregnancies, 7391 (50%) in Sweden, 2885 (49%) in Finland, and 6150 (51%) in Denmark were categorized as HDFN pregnancies. Maternal complications and stillbirth rates were comparable between HDFN and non-HDFN pregnancies. Caesarean deliveries were more frequent in HDFN pregnancies. A total of 14,519 neonates in Sweden, 5827 in Finland, and 11,803 in Denmark were born to all pregnancies identified. Of these, 7289 (50%), 2849 (49%), and 6076 (51%) had HDFN. Among the neonates with HDFN, 27% in Sweden, 38% in Finland, and 12% in Denmark received HDFN-related treatment, including intrauterine transfusion (IUT; data unavailable for Finland), neonatal transfusion, and phototherapy. Compared to non-HDFN neonates, those in the IUT and neonatal transfusion groups had lower gestational age, birth weight and length, and higher rates of neonatal unit admission, and were more frequently diagnosed postnatally with growth disturbances and disorders of the nervous system. Conclusion: This is a comprehensive overview of perinatal characteristics and outcomes of pregnancies at risk of HDFN in Sweden, Finland, and Denmark. Our findings highlight the significant unmet need in perinatal care among neonates with HDFN, particularly those treated with IUT or neonatal transfusion. Further research is warranted to improve the management of severe HDFN pregnancies.

Indexed as

Alloimmunizationhemolytic disease of the fetus and newbornintrauterine transfusionneonatal outcomespopulation-based studypregnancy outcomes

Identifiers

PMID40792190
PMCPMC12337666

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