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


Journal

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology
ISSN: 1469-0705
Titre abrégé: Ultrasound Obstet Gynecol
Pays: England
ID NLM: 9108340

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 04 05 2018
revised: 11 06 2018
accepted: 14 06 2018
pubmed: 28 6 2018
medline: 3 5 2019
entrez: 28 6 2018
Statut: ppublish

Résumé

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. 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. 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. 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.

Identifiants

pubmed: 29947159
doi: 10.1002/uog.19164
doi:

Substances chimiques

Immunoglobulin G 0
Immunoglobulins 0

Types de publication

Comparative Study Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

383-389

Informations de copyright

Copyright © 2018 ISUOG. Published by John Wiley & Sons Ltd.

Auteurs

K O Kagan (KO)

Department of Women's Health, University of Tübingen, Tübingen, Germany.

M Enders (M)

Laboratory Prof. Gisela Enders & Colleagues MVZ and Institute of Virology, Infectiology and Epidemiology e.V, Stuttgart, Germany.

M S Schampera (MS)

Institute of Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.

E Baeumel (E)

Institute of Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.

M Hoopmann (M)

Department of Women's Health, University of Tübingen, Tübingen, Germany.

A Geipel (A)

Department of Obstetrics and Gynaecology, University of Bonn, Bonn, Germany.

C Berg (C)

Department of Obstetrics and Gynaecology, University of Cologne, Cologne, Germany.

R Goelz (R)

Department of Neonatology, University of Tübingen, Tübingen, Germany.

L De Catte (L)

Department of Obstetrics and Gynaecology, University of Leuven, Leuven, Belgium.

D Wallwiener (D)

Department of Women's Health, University of Tübingen, Tübingen, Germany.

S Brucker (S)

Department of Women's Health, University of Tübingen, Tübingen, Germany.

S P Adler (SP)

CMV Research Foundation, Richmond, VA, USA.

G Jahn (G)

Institute of Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.

K Hamprecht (K)

Institute of Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.

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Classifications MeSH