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Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report

BACKGROUND: Parvovirus is a common childhood infection that could be very dangerous to the fetus, if pregnant women become infected. The spectrum of effects range from pure red blood cell aplasia with hydrops fetalis to meningoencephalitis, with many symptoms in between. Severe anemia in the setting...

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Autores principales: Aronson, Stephanie T., Celiker, Mahmut Y., Guarini, Ludovico, Agha, Rabia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405454/
https://www.ncbi.nlm.nih.gov/pubmed/37544998
http://dx.doi.org/10.1186/s40748-023-00164-2
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author Aronson, Stephanie T.
Celiker, Mahmut Y.
Guarini, Ludovico
Agha, Rabia
author_facet Aronson, Stephanie T.
Celiker, Mahmut Y.
Guarini, Ludovico
Agha, Rabia
author_sort Aronson, Stephanie T.
collection PubMed
description BACKGROUND: Parvovirus is a common childhood infection that could be very dangerous to the fetus, if pregnant women become infected. The spectrum of effects range from pure red blood cell aplasia with hydrops fetalis to meningoencephalitis, with many symptoms in between. Severe anemia in the setting of pure red blood cell aplasia is one of the more common effects that neonatal experience (if infected intrapartum), with the current gold standard treatment being intrauterine or postnatal packed red blood cell (PRBC) transfusions, yet intravenous immunoglobulin (IVIG) may be a superior treatment option. CASE PRESENTATION: A preterm infant was born at 26th week of gestational age via emergency Cesarean section due to hydrops fetalis, with parvovirus B19 exposure one month prior. The infant tested positive for IgM antibodies against parvovirus B19. Among many other serious complications of both hydrops fetalis and premature delivery, the infant had severe unremitting anemia, and received many PRBC transfusion over the course of his 71-day-long neonatal intensive care unit stay. During a follow up appointments as outpatient, his blood tests showed persistent high copies of parvovirus B19. He was then supported with PRBC transfusions and treated with IVIG. After three doses of IVIG, the infant’s parvovirus B19 viral copy numbers have dramatically reduced and the infant did not require any more PRBC transfusions. CONCLUSIONS: IVIG infusion effectively treated the parvovirus B19 infection and restored erythropoiesis making the child transfusion independent. Furthermore, since IVIG is safe and readily crosses the placenta, further studies are needed to determine if IVIG should be considered as an alternative prenatal treatment for congenital parvovirus B19 infection.
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spelling pubmed-104054542023-08-08 Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report Aronson, Stephanie T. Celiker, Mahmut Y. Guarini, Ludovico Agha, Rabia Matern Health Neonatol Perinatol Case Report BACKGROUND: Parvovirus is a common childhood infection that could be very dangerous to the fetus, if pregnant women become infected. The spectrum of effects range from pure red blood cell aplasia with hydrops fetalis to meningoencephalitis, with many symptoms in between. Severe anemia in the setting of pure red blood cell aplasia is one of the more common effects that neonatal experience (if infected intrapartum), with the current gold standard treatment being intrauterine or postnatal packed red blood cell (PRBC) transfusions, yet intravenous immunoglobulin (IVIG) may be a superior treatment option. CASE PRESENTATION: A preterm infant was born at 26th week of gestational age via emergency Cesarean section due to hydrops fetalis, with parvovirus B19 exposure one month prior. The infant tested positive for IgM antibodies against parvovirus B19. Among many other serious complications of both hydrops fetalis and premature delivery, the infant had severe unremitting anemia, and received many PRBC transfusion over the course of his 71-day-long neonatal intensive care unit stay. During a follow up appointments as outpatient, his blood tests showed persistent high copies of parvovirus B19. He was then supported with PRBC transfusions and treated with IVIG. After three doses of IVIG, the infant’s parvovirus B19 viral copy numbers have dramatically reduced and the infant did not require any more PRBC transfusions. CONCLUSIONS: IVIG infusion effectively treated the parvovirus B19 infection and restored erythropoiesis making the child transfusion independent. Furthermore, since IVIG is safe and readily crosses the placenta, further studies are needed to determine if IVIG should be considered as an alternative prenatal treatment for congenital parvovirus B19 infection. BioMed Central 2023-08-07 /pmc/articles/PMC10405454/ /pubmed/37544998 http://dx.doi.org/10.1186/s40748-023-00164-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Case Report
Aronson, Stephanie T.
Celiker, Mahmut Y.
Guarini, Ludovico
Agha, Rabia
Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report
title Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report
title_full Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report
title_fullStr Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report
title_full_unstemmed Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report
title_short Intravenous immunoglobulin treatment of congenital parvovirus B19 induced anemia - a case report
title_sort intravenous immunoglobulin treatment of congenital parvovirus b19 induced anemia - a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10405454/
https://www.ncbi.nlm.nih.gov/pubmed/37544998
http://dx.doi.org/10.1186/s40748-023-00164-2
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