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Published on: July 24, 2016
Prenatal parvovirus B19 infection
Karl Oliver Kagan1, Markus Hoopmann2, Annegret Geipel3
1Department of Obstetrics and Gynaecology, University Hospital Tuebingen, Calwerstrasse 7, 72076, Tuebingen, Germany. KOKagan@gmx.de.
Insights
Parvovirus B19 infection during pregnancy can lead to fetal complications like anemia and hydrops fetalis. Early monitoring and intervention, including intrauterine transfusions, are crucial for managing severe cases.
Area of Science:
- Virology
- Obstetrics
- Pediatrics
Background:
- Parvovirus B19 (B19V) causes fifth disease, typically mild in children.
- Pregnant women not immune to B19V are at risk for primary infection.
- B19V infection in pregnancy poses risks including fetal anemia, hydrops fetalis, miscarriage, and intrauterine fetal death.
Purpose of the Study:
- To provide a comprehensive overview of B19V infection in pregnancy.
- To detail the epidemiology, pathogenesis, clinical features, diagnosis, and management of B19V during gestation.
Main Methods:
- Review of existing literature on B19V infection in pregnancy.
- Discussion of diagnostic methods including ultrasound and Doppler studies.
- Outline of management strategies, including fetal blood sampling and intrauterine transfusions.
Main Results:
- Maternal-fetal transmission occurs in 30-50% of primary B19V infections during pregnancy.
- Risk of fetal anemia or hydrops is 3-4% overall, increasing to 6-7% if infection occurs before 20 weeks gestation.
- Fetal monitoring involves ultrasounds and Doppler measurements; intrauterine transfusions are used for severe fetal anemia.
Conclusions:
- B19V infection during pregnancy requires careful monitoring due to potential severe fetal outcomes.
- Timely diagnosis and intervention, such as intrauterine transfusions, can improve fetal prognosis.
- Understanding B19V's impact is vital for obstetric and pediatric care providers.
Abstract:
Parvovirus B19 (B19V) causes erythema infectiosum, a.k.a., fifth disease. This disease primarily affects children. It is generally self-limiting and subsides after 1-2 weeks. In pregnancy, the virus can cross the placenta and result in a fetal infection. This may lead to severe fetal anemia, hydrops fetalis, a miscarriage, or intrauterine fetal death. The risk of long-term sequelae also appears to be increased. About one-third of pregnant women are not immune to B19V and, therefore, are at risk to contract a primary infection. The seroconversion rate during pregnancy is generally around 1-2%. During a primary infection, maternal-fetal transplacental transmission of B19V occurs in about 30-50% of the cases and the risk of fetal infection increases with advancing gestational age. The risk of severe fetal anemia or hydrops is around 3-4% overall and is around 6-7% if the primary infection occurs before 20 weeks' gestation. Fetal monitoring in women with a primary B19V infection includes regular ultrasound examinations looking for evidence of hydrops fetalis and Doppler measurements of the middle cerebral artery peak velocity. Fetal blood sampling is performed if a significant anemia is suspected and, if such is found, an intrauterine blood transfusion is needed. This article provides an overview of the epidemiology, pathogenesis, clinical manifestations, diagnostic methods, and management of B19V infection during pregnancy.
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