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Variations and Opportunities in Postnatal Management of Hemolytic Disease of the Fetus and Newborn
De Winter, D.P. (Sanquin Diagnostic Services)
Verweij, E.J.T. (Leiden University Medical Center)
Debeer, A. (University Hospitals Leuven (Bèlgica))
Devlieger, Roland (University Hospitals Leuven (Bèlgica))
Lewi, L. (University Hospitals Leuven (Bèlgica))
Verbeeck, S. (University Hospitals Leuven (Bèlgica))
Maurice, P. (Sorbonne University)
Jouannic, J.M. (Sorbonne University)
Guillemin, M.G. (Sorbonne University)
Mailloux, A. (Sorbonne University)
Pessoa Dos Santos, M.C. (Instituto Nacional de Saúde da Mulher. da Criança e do Adolescente Fernandes Figueira (IFF/Fiocruz))
Amaral De Moura Sá Pacheco, C. (Instituto Nacional de Saúde da Mulher. da Criança e do Adolescente Fernandes Figueira (IFF/Fiocruz))
Lopes Moreira, M.E. (Instituto Nacional de Saúde da Mulher. da Criança e do Adolescente Fernandes Figueira (IFF/Fiocruz))
Martins De Vasconcelos Vaena, M. (Instituto Nacional de Saúde da Mulher. da Criança e do Adolescente Fernandes Figueira (IFF/Fiocruz))
Bohlin, K. (Karolinska Institutet)
Tiblad, E. (Umeå University Hospital)
Thorup, E. (University of Copenhagen)
Petersen, O.B. (University of Copenhagen)
Sanchez-Holgado, M. (Hospital Universitario La Paz (Madrid))
Viejo Llorente, A. (Hospital Universitario La Paz (Madrid))
Poljak, B. (Liverpool Women's Hospital NHS Foundation Trust)
Khalil, A. (St George's Hospital. St George's University of London)
Le Duc, K. (Université de Lille. CHU Lille)
Ghesquiere, L. (Université de Lille. CHU Lille)
Lozar Krivec, J. (Univerza V Ljubljani)
Soltirovska-Šalamon, A. (Univerza V Ljubljani)
Dame, C. (Charité-Universitätsmedizin Berlin)
Blank, J.D. (Charité-Universitätsmedizin Berlin)
Hohnecker, A. (Kinderklinik des Klinikums Dritter Orden. Klinikums Dritter Orden)
Saxonhouse, M. (Atrium Healthcare Levine Children's Hospital)
Connors, N.K. (Atrium Healthcare Carolinas Medical Center)
Geipel, A. (University Hospital Bonn (Bonn, Alemanya))
Rath, J. (University Hospital Bonn (Bonn, Alemanya))
Prasad, S. (St George's Hospital. St George's University of London)
Van Wyk, L. (Stellenbosch University and Tygerberg Hospital)
Geerts, L. (Stellenbosch University)
Schuler, R. (Justus-Liebig-University)
Thon, N. (Justus-Liebig-University)
Leibovitch, L. (Sheba Medical Center)
Cohen, S. (Tel Aviv University)
Canul-Euan, A.A. (National Institute of Perinatology)
Kelly, E. (University of Toronto)
Raghuram, K. (University of Toronto)
Cavigioli, F. (University of Milan)
Colombo, S.F.G. (University of Milan)
Elanjikal, Z. (University Hospitals Bristol and Weston NHS Trust)
Brayley, J. (University Hospitals Bristol and Weston NHS Trust)
Pfurtscheller, D. (Medical University of Graz)
Pichler, G. (Medical University of Graz)
Alcázar Grisi, Á.G. (Hospital de La Mujer)
Chávez Navarro, E.J.J. (Hospital de La Mujer)
Pereira-Nunes, J. (Porto University)
Soares, H. (Porto University)
Zhou, M. (Tongji University School of Medicine)
Garcia Borau, Maria José (Institut de Recerca Sant Pau)
Moliner Calderón, E. (Institut de Recerca Sant Pau)
Galletti, M.F. (Instituto Universitario Hospital Italiano de Buenos Aires)
Mariani, G.L. (Instituto Universitario Hospital Italiano de Buenos Aires)
Mackin, D. (Royal Women's Hospital Melbourne)
Malone, F. (Rotunda Hospital Dublin)
Lampland, A. (Children's Minnesota)
Tse, W.T. (The Chinese University of Hong Kong)
Castleman, J. (Birmingham Women's and Children's NHS Foundation Trust)
Van Der Bom, J.G. (Leiden University Medical Center)
De Haas, M. (Leiden University Medical Center)
Lopriore, E. (Leiden University Medical Center)
Universitat Autònoma de Barcelona

Date: 2025
Abstract: Importance: Preventive efforts in pregnancy-related alloimmunization have considerably decreased the prevalence of hemolytic disease of the fetus and newborn (HDFN). International studies are therefore essential to obtain a deeper understanding of the postnatal management and outcomes of HDFN. Taken together with numerous treatment options, large practice variations among centers may exist. Objectives: To assess variations in postnatal management and outcomes of HDFN among international centers and to identify opportunities to improve care. Design, Setting, and Participants: In this international, retrospective, cohort study, 31 expert centers from 22 countries retrieved data on neonates with HDFN managed between January 1, 2006, and July 1, 2021. Statistical analysis was performed from July 19, 2023, to October 28, 2024. Main Outcomes and Measures: Main outcomes included the frequency of exchange transfusions, administration of intravenous immunoglobulin, administration of erythropoiesis-stimulating agents, and red blood cell transfusions, as well as the association of gestational age at birth with exchange transfusion frequency and risk factors for adverse neonatal outcomes. Results: The study included 1855 neonates (median gestational age at birth, 36. 4 weeks [IQR, 35. 0-37. 3 weeks]; 1034 boys [55. 7%]), of whom 1017 (54. 8%) received any form of antenatal treatment. Most neonates (1447 [78. 0%]) had anti-D antibodies. Exchange transfusions were performed in 436 neonates (23. 5%), with proportions in exchange transfusion frequency varying from 0% to 78% among centers. Intravenous immunoglobulin was administered to 429 of 1743 neonates (24. 6%), with proportions varying from 0% to 100% among centers. A higher gestational age at birth was associated with a reduction in exchange transfusion frequency in neonates with intrauterine transfusion, decreasing from approximately 38. 2% (13 of 34) at 34 weeks to 16. 8% (18 of 107) after 37 weeks and 0 days. A weekly increase in gestational age at birth was associated with a 43. 3% decrease (95% CI, 36. 1%-49. 7%) in the likelihood of adverse neonatal outcomes, and neonates who received an exchange transfusion were 1. 55 (95% CI, 1. 10-2. 18) times more likely to experience unfavorable outcomes. Conclusions and Relevance: In this cohort study of neonates with HDFN managed at 31 centers in 22 countries, significant practice variations in the postnatal management of HDFN were identified, highlighting the lack of, and need for, consensus. The study suggests that there is a potential beneficial clinical association of waiting for delivery until after 37 weeks and 0 days with frequency of exchange transfusions among neonates with HDFN. The framework to implement international guidelines is provided.
Rights: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Language: Anglès
Document: Article ; recerca ; Versió publicada
Subject: Erythroblastosis, Fetal ; Erythrocyte Transfusion ; Exchange Transfusion, Whole Blood ; Female ; Gestational Age ; Humans ; Immunoglobulins, Intravenous ; Infant, Newborn ; Male ; Postnatal Care ; Pregnancy ; Retrospective Studies
Published in: JAMA network open, Vol. 8 Núm. 1 (october 2025) , p. e2454330, ISSN 2574-3805

DOI: 10.1001/jamanetworkopen.2024.54330
PMID: 39792381


13 p, 1.1 MB

The record appears in these collections:
Research literature > UAB research groups literature > Research Centres and Groups (research output) > Health sciences and biosciences > Institut de Recerca Sant Pau
Articles > Research articles
Articles > Published articles

 Record created 2025-10-01, last modified 2026-01-02



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