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Hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape

BACKGROUND: Prevention of pregnancy-related alloimmunization and the management of hemolytic disease of the fetus and newborn (HDFN) has significantly improved over the past decades. Considering improvements in HDFN care, the objectives of this systematic literature review were to assess the prenata...

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Autores principales: de Winter, Derek P., Kaminski, Allysen, Tjoa, May Lee, Oepkes, Dick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824959/
https://www.ncbi.nlm.nih.gov/pubmed/36611144
http://dx.doi.org/10.1186/s12884-022-05329-z
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author de Winter, Derek P.
Kaminski, Allysen
Tjoa, May Lee
Oepkes, Dick
author_facet de Winter, Derek P.
Kaminski, Allysen
Tjoa, May Lee
Oepkes, Dick
author_sort de Winter, Derek P.
collection PubMed
description BACKGROUND: Prevention of pregnancy-related alloimmunization and the management of hemolytic disease of the fetus and newborn (HDFN) has significantly improved over the past decades. Considering improvements in HDFN care, the objectives of this systematic literature review were to assess the prenatal treatment landscape and outcomes of Rh(D)- and K-mediated HDFN in mothers and fetuses, to identify the burden of disease, to identify evidence gaps in the literature, and to provide recommendations for future research. METHODS: We performed a systematic search on MEDLINE, EMBASE and clinicaltrials.gov. Observational studies, trials, modelling studies, systematic reviews of cohort studies, and case reports and series of women and/or their fetus with HDFN caused by Rhesus (Rh)D or Kell alloimmunization. Extracted data included prevalence; treatment patterns; clinical outcomes; treatment efficacy; and mortality. RESULTS: We identified 2,541 articles. After excluding 2,482 articles and adding 1 article from screening systematic reviews, 60 articles were selected. Most abstracted data were from case reports and case series. Prevalence was 0.047% and 0.006% for Rh(D)- and K-mediated HDFN, respectively. Most commonly reported antenatal treatment was intrauterine transfusion (IUT; median frequency [interquartile range]: 13.0% [7.2–66.0]). Average gestational age at first IUT ranged between 25 and 27 weeks. weeks. This timing is early and carries risks, which were observed in outcomes associated with IUTs. The rate of hydrops fetalis among pregnancies with Rh(D)-mediated HDFN treated with IUT was 14.8% (range, 0–50%) and 39.2% in K-mediated HDFN. Overall mean ± SD fetal mortality rate that was found to be 19.8%±29.4% across 19 studies. Mean gestational age at birth ranged between 34 and 36 weeks. CONCLUSION: These findings corroborate the rareness of HDFN and frequently needed intrauterine transfusion with inherent risks, and most births occur at a late preterm gestational age. We identified several evidence gaps providing opportunities for future studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-022-05329-z.
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spelling pubmed-98249592023-01-08 Hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape de Winter, Derek P. Kaminski, Allysen Tjoa, May Lee Oepkes, Dick BMC Pregnancy Childbirth Research BACKGROUND: Prevention of pregnancy-related alloimmunization and the management of hemolytic disease of the fetus and newborn (HDFN) has significantly improved over the past decades. Considering improvements in HDFN care, the objectives of this systematic literature review were to assess the prenatal treatment landscape and outcomes of Rh(D)- and K-mediated HDFN in mothers and fetuses, to identify the burden of disease, to identify evidence gaps in the literature, and to provide recommendations for future research. METHODS: We performed a systematic search on MEDLINE, EMBASE and clinicaltrials.gov. Observational studies, trials, modelling studies, systematic reviews of cohort studies, and case reports and series of women and/or their fetus with HDFN caused by Rhesus (Rh)D or Kell alloimmunization. Extracted data included prevalence; treatment patterns; clinical outcomes; treatment efficacy; and mortality. RESULTS: We identified 2,541 articles. After excluding 2,482 articles and adding 1 article from screening systematic reviews, 60 articles were selected. Most abstracted data were from case reports and case series. Prevalence was 0.047% and 0.006% for Rh(D)- and K-mediated HDFN, respectively. Most commonly reported antenatal treatment was intrauterine transfusion (IUT; median frequency [interquartile range]: 13.0% [7.2–66.0]). Average gestational age at first IUT ranged between 25 and 27 weeks. weeks. This timing is early and carries risks, which were observed in outcomes associated with IUTs. The rate of hydrops fetalis among pregnancies with Rh(D)-mediated HDFN treated with IUT was 14.8% (range, 0–50%) and 39.2% in K-mediated HDFN. Overall mean ± SD fetal mortality rate that was found to be 19.8%±29.4% across 19 studies. Mean gestational age at birth ranged between 34 and 36 weeks. CONCLUSION: These findings corroborate the rareness of HDFN and frequently needed intrauterine transfusion with inherent risks, and most births occur at a late preterm gestational age. We identified several evidence gaps providing opportunities for future studies. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12884-022-05329-z. BioMed Central 2023-01-07 /pmc/articles/PMC9824959/ /pubmed/36611144 http://dx.doi.org/10.1186/s12884-022-05329-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
de Winter, Derek P.
Kaminski, Allysen
Tjoa, May Lee
Oepkes, Dick
Hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape
title Hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape
title_full Hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape
title_fullStr Hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape
title_full_unstemmed Hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape
title_short Hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape
title_sort hemolytic disease of the fetus and newborn: systematic literature review of the antenatal landscape
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9824959/
https://www.ncbi.nlm.nih.gov/pubmed/36611144
http://dx.doi.org/10.1186/s12884-022-05329-z
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