Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/24442
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dc.contributor.authorAttwood, Lucy O-
dc.contributor.authorHolmes, Natasha E-
dc.contributor.authorHui, Lisa-
dc.date2020-08-29-
dc.date.accessioned2020-09-28T20:38:22Z-
dc.date.available2020-09-28T20:38:22Z-
dc.date.issued2020-12-
dc.identifier.citationPrenatal Diagnosis 2020; 40(13): 1722-1731en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/24442-
dc.description.abstractParvovirus B19 (B19V) infection is well known for its mild, self-limiting clinical presentations in children, such as erythema infectiosum. Approximately 40% of women of childbearing age are susceptible to B19V infection. While maternal B19V infection usually has a good prognosis, B19V can cause severe fetal anaemia and pregnancy loss due to its ability to suppress erythroid progenitor cells. Noninvasive ultrasound monitoring for fetal anaemia is usually performed if maternal seroconversion occurs in the first 20 weeks of gestation, with amniocentesis for fetal infection reserved for those who first present with fetal anaemia or hydrops of unknown cause. Intrauterine transfusion is the standard treatment for severe fetal anaemia and is associated with a significant improvement in survival. However, survivors of hydrops fetalis may have a higher rate of long-term neurodevelopmental complications compared with nonhydropic survivors. This review aims to synthesise published data on the diagnosis, surveillance and outcomes of congenital parvovirus infection to assist clinicians in diagnosing and managing this important condition. This article is protected by copyright. All rights reserved.en
dc.language.isoeng-
dc.titleIdentification and management of congenital parvovirus B19 infection.en
dc.typeJournal Articleen
dc.identifier.journaltitlePrenatal Diagnosisen
dc.identifier.affiliationDepartment of Perinatal Medicine, Mercy Hospital for Women, Melbourne, Australiaen
dc.identifier.affiliationInfectious Diseasesen
dc.identifier.affiliationDepartment of Obstetrics and Gynaecology, Northern Healthen
dc.identifier.affiliationReproductive Epidemiology group, Murdoch Children's Research Instituteen
dc.identifier.affiliationDepartment of Obstetrics and Gynaecology, The University of Melbourne, Australiaen
dc.identifier.affiliationDepartment of Medicine and Radiology, The University of Melbourne, Australiaen
dc.identifier.doi10.1002/pd.5819en
dc.type.contentTexten
dc.identifier.orcid0000-0003-0447-7917en
dc.identifier.orcid0000-0002-9720-3562en
dc.identifier.orcid0000-0001-8501-4054-
dc.identifier.pubmedid32860469-
local.name.researcherHolmes, Natasha E
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
crisitem.author.deptInfectious Diseases-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
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