Fetal and maternal outcome after hyperimmunoglobulin administration for prevention of maternal-fetal transmission of cytomegalovirus during pregnancy: retrospective cohort analysis
- PMID: 32754858
- PMCID: PMC7584525
- DOI: 10.1007/s00404-020-05728-7
Fetal and maternal outcome after hyperimmunoglobulin administration for prevention of maternal-fetal transmission of cytomegalovirus during pregnancy: retrospective cohort analysis
Abstract
Purpose: To determine the frequency of fetal infection as well as adverse pregnancy outcomes following antenatal hyperimmunoglobulin (HIG) treatment for primary cytomegalovirus (CMV) infection in pregnancy.
Methods: In our observational cohort study, data from 46 women with a primary CMV infection during pregnancy were evaluated. Primary CMV infection was defined by seroconversion or the presence of CMV-IgM and low CMV-IgG avidity. All women received at least two or more infusions of HIG treatment (200 IU/kg). Congenital CMV infection (cCMV) was diagnosed by detection of CMV in amniotic fluid and/or neonatal urine. We compared the rate of maternal-fetal transmission from our cohort to data without treatment in the literature. The frequency of adverse pregnancy outcomes was compared to those of live-born infants delivered in our clinic.
Results: We detected 11 intrauterine infections in our cohort, which correlates to a transmission rate of 23.9%. Compared to the transmission rate found in cases without treatment (39.9%), this is a significant reduction (P = 0.026). There were no adverse pregnancy outcomes in our cohort. The mean gestational age at delivery was 39 weeks gestation in treatment and control group.
Conclusion: The administration of HIG for prevention of maternal-fetal CMV transmission during pregnancy seems safe and effective.
Keywords: Cytomegalovirus; Fetal transmission; Hyperimmunoglobulin; Pregnancy; Prevention of maternal.
Conflict of interest statement
VS, MH, RCR, and WH declare that they have no conflict of interest. JPS has served as local PI in a prospective randomized trial on Cytotect® conducted by Biotest AG, Dreieich Germany. In this position, he has received travel grants to a study meeting and a conference on CMV in 2016.
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