Prevention of maternal–fetal transmission of cytomegalovirus after primary maternal infection in the first trimester by biweekly hyperimmunoglobulin administration

医学 羊膜穿刺术 巨细胞病毒 妊娠期 产科 怀孕 胎龄 胎儿 前瞻性队列研究 子宫内 妇科 儿科 产前诊断 外科 疱疹病毒科 病毒性疾病 免疫学 人类免疫缺陷病毒(HIV) 遗传学 生物
作者
K. O. Kagan,Martin Enders,Matthias Stefan Schampera,E. Baeumel,Markus Hoopmann,Annegret Geipel,Christoph Berg,Rangmar Goelz,Luc De Catte,D. Wallwiener,Sara Y. Brucker,S. P. Adler,Gerhard Jahn,Klaus Hamprecht
出处
期刊:Ultrasound in Obstetrics & Gynecology [Wiley]
卷期号:53 (3): 383-389 被引量:130
标识
DOI:10.1002/uog.19164
摘要

ABSTRACT Objective To examine the efficacy of biweekly hyperimmunoglobulin (HIG) administration to prevent maternal–fetal transmission of cytomegalovirus (CMV) in women with primary first‐trimester CMV infection. Methods This was a prospective observational study of women with confirmed primary CMV infection in the first trimester who had the first HIG administration at or before 14 weeks' gestation. All women had biweekly HIG treatment until 20 weeks' gestation at a dose of 200 IU/kg of maternal body weight. Each subject underwent amniocentesis at least 6 weeks after first presentation at about 20 weeks. Primary outcome was maternal–fetal transmission at the time of amniocentesis, and secondary outcome was the frequency of congenital CMV infection at birth. The results were compared with a historic cohort of women with first‐trimester CMV infection who did not undergo HIG treatment and who had amniocentesis at about 20 weeks. Results Subjects were 40 pregnant women with a primary CMV infection, with a median gestational age at first presentation of 9.6 (range, 5.1–14.3) weeks. On average, HIG administration started at 11.1 weeks and continued until 16.6 weeks. Within this interval, HIG was administered between two and six times in each patient. While CMV immunoglobulin‐G (IgG) monitoring showed periodic fluctuations during biweekly HIG administration cycles, high CMV‐IgG avidity indices remained stable over the whole treatment period. Maternal–fetal transmission before amniocentesis occurred in only one of the 40 cases (2.5% (95% CI, 0–13.2%)). At delivery, two additional subjects were found to have had late‐gestation transmission. Considering all three cases with maternal–fetal transmission, the transmission rate was 7.5% (95% CI, 1.6–20.4%) in our 40 cases. All infected neonates were asymptomatic at birth. The matched historical control group consisted of 108 pregnancies. Thirty‐eight transmissions (35.2% (95% CI, 26.2–45.0%)) occurred in the control group, which was significantly higher ( P < 0.0001) than the transmission rate in the HIG treatment group. Conclusion After a primary maternal CMV infection in the first trimester, biweekly HIG administration at a dose of 200 IU/kg prevents maternal–fetal transmission up to 20 weeks' gestation. Copyright © 2018 ISUOG. Published by John Wiley & Sons Ltd.
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