First-line noninvasive management of cytomegalovirus primary infection in pregnancy
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Marie Denef
, Laure Noel
, Gaëlle Bruck , Justine Gudelj , Malek Tebache , Renaud Viellevoye , Michelle Nisolle and Frédéric Chantraine
Abstract
Objectives
To introduce a first-line noninvasive antenatal management of maternal cytomegalovirus (CMV) primary infection based on ultrasound (US) and magnetic resonance imaging (MRI). Amniocentesis (AC) is used as a second-line tool in cases of abnormalities compatible with fetal CMV infection on US and/or MRI screening.
Methods
Between January 2011 and October 2018, pregnant women referred with a CMV primary infection on antibody screening were followed up by monthly US scans and a brain MRI at approximately 32 weeks. In cases with US and/or MRI abnormalities compatible with congenital CMV infection, AC was performed to confirm the diagnosis.
Results
Ninety pregnant women with a primary CMV infection were included (89 singleton and one twin pregnancy). The first-line screening by US and/or MRI was normal for 72 of 91 fetuses (79%). At birth, 19 of these 72 neonates (26%) had a positive urine sample for CMV but were asymptomatic. US and/or MRI abnormalities were identified in 19 fetuses (21%). AC confirmed a fetal CMV infection in 16 fetuses (84%); 12 pregnancies were terminated, and four were continued, with three symptomatic neonates at birth and one poor neurodevelopmental outcome at postnatal follow-up.
Conclusions
First-line noninvasive management of maternal CMV primary infection based on serial US scans and brain MRI can be offered to identify fetuses with severe symptomatic congenital CMV infection and reduce the number of ACs without compromising the fetal outcome.
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Research funding: None declared.
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Author contributions: Conceptualization: MD, LN, FC; Methodology: MD, LN, FC; Data collection: MD, LN, GB, JG; Data interpretation: MD, LN, MT, RV, FC; Manuscript draft: MD, LN; Manuscript review & editing: MD, LN, MT, RV, MN, FC. All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: The authors state no conflicts of interest.
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Informed consent: Informed consent was obtained from all individuals included in this study.
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Ethical approval: Research involving human subjects complied with all relevant national regulations and institutional policies and was in accordance with the tenets of the Helsinki Declaration (as revised in 2013). Approved by the authors’ Institutional Review Board or equivalent committee (JL/bl/1870 – B4122020000011).
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Supplementary Material
The online version of this article offers supplementary material (https://doi.org/10.1515/jpm-2021-0384).
© 2021 Walter de Gruyter GmbH, Berlin/Boston
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