What type of infection, parvovirus (Parvovirus B19) or varicella, is most likely associated with Intrauterine Fetal Death (IUFD)?

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From the Guidelines

Parvovirus B19 infection is more likely associated with intrauterine fetal death (IUFD) compared to varicella. This is because maternal parvovirus B19 infection, especially during the first 20 weeks of pregnancy, can lead to severe fetal anemia by directly infecting and destroying erythroid progenitor cells in the fetal bone marrow, as reported in the study by 1. The severe anemia caused by parvovirus B19 infection can result in high-output cardiac failure, hydrops fetalis, and ultimately intrauterine fetal death in approximately 5-10% of infected fetuses, with the risk being highest when maternal infection occurs between 9-20 weeks gestation when fetal red blood cell production is primarily in the liver and the fetus has a shorter red cell lifespan. While varicella (chickenpox) during pregnancy can cause complications including congenital varicella syndrome with limb hypoplasia, skin scarring, and neurological abnormalities, it less commonly results in IUFD, as noted in the study by 1. Management of confirmed maternal parvovirus infection includes serial ultrasounds to monitor for signs of fetal anemia or hydrops, with consideration for intrauterine transfusion if severe fetal anemia develops, which can significantly improve survival rates in hydropic fetuses, as shown in the studies by 1 and 1. Key points to consider in the management of parvovirus B19 infection in pregnancy include:

  • Serial ultrasounds to monitor for signs of fetal anemia or hydrops
  • Consideration for intrauterine transfusion if severe fetal anemia develops
  • Awareness of the potential for delayed psychomotor development and abnormal neurological outcomes in survivors of nonimmune hydrops fetalis, as reported in the study by 1. Overall, the evidence suggests that parvovirus B19 infection is a significant risk factor for IUFD, and prompt diagnosis and management are essential to improve outcomes, as emphasized in the study by 1.

From the Research

Infection Association with IUFD

  • Parvovirus B19 infection is a significant cause of Intrauterine Fetal Death (IUFD) due to its effects on fetal erythropoiesis, leading to anemia, hydrops fetalis, and ultimately fetal death 2, 3, 4, 5, 6.
  • The risk of fetal death is higher when maternal parvovirus B19 infection occurs before 20 weeks of gestation 5.
  • Varicella infection is not mentioned in the provided studies as a common cause of IUFD, whereas parvovirus B19 is consistently associated with IUFD in the literature 2, 3, 4, 5, 6.

Comparison of Infections

  • Parvovirus B19 infection can cause severe hydrops fetalis, which may result in fetal death if left untreated 3, 5, 6.
  • In contrast, there is no direct evidence in the provided studies linking varicella infection to IUFD, making parvovirus B19 a more likely cause of IUFD based on the available data 2, 3, 4, 5, 6.

Clinical Presentation

  • Parvovirus B19-associated IUFD can present with or without signs of fetal hydrops, with the latter being more common in late gestation 4.
  • Early diagnosis and treatment of parvovirus B19 infection are crucial in preventing fetal complications, including IUFD 2, 5, 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Parvovirus B19 infection in pregnancy.

Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 2006

Research

Long-term outcome in fetal hydrops from parvovirus B19 infection.

American journal of obstetrics and gynecology, 1992

Research

Revised clinical presentation of parvovirus B19-associated intrauterine fetal death.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2002

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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