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Prevention of maternal-fetal transmission of cytomegalovirus after primary maternal infection in the first trimester by biweekly hyperimmunoglobulin administration.
Kagan, K O; Enders, M; Schampera, M S; Baeumel, E; Hoopmann, M; Geipel, A; Berg, C; Goelz, R; De Catte, L; Wallwiener, D; Brucker, S; Adler, S P; Jahn, G; Hamprecht, K.
Afiliación
  • Kagan KO; Department of Women's Health, University of Tübingen, Tübingen, Germany.
  • Enders M; Laboratory Prof. Gisela Enders & Colleagues MVZ and Institute of Virology, Infectiology and Epidemiology e.V, Stuttgart, Germany.
  • Schampera MS; Institute of Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.
  • Baeumel E; Institute of Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.
  • Hoopmann M; Department of Women's Health, University of Tübingen, Tübingen, Germany.
  • Geipel A; Department of Obstetrics and Gynaecology, University of Bonn, Bonn, Germany.
  • Berg C; Department of Obstetrics and Gynaecology, University of Cologne, Cologne, Germany.
  • Goelz R; Department of Neonatology, University of Tübingen, Tübingen, Germany.
  • De Catte L; Department of Obstetrics and Gynaecology, University of Leuven, Leuven, Belgium.
  • Wallwiener D; Department of Women's Health, University of Tübingen, Tübingen, Germany.
  • Brucker S; Department of Women's Health, University of Tübingen, Tübingen, Germany.
  • Adler SP; CMV Research Foundation, Richmond, VA, USA.
  • Jahn G; Institute of Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.
  • Hamprecht K; Institute of Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.
Ultrasound Obstet Gynecol ; 53(3): 383-389, 2019 Mar.
Article en En | MEDLINE | ID: mdl-29947159
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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_doencas_nao_transmissiveis Asunto principal: Inmunoglobulinas / Infecciones por Citomegalovirus / Transmisión Vertical de Enfermedad Infecciosa / Citomegalovirus / Enfermedades Fetales Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Ultrasound Obstet Gynecol Asunto de la revista: DIAGNOSTICO POR IMAGEM / GINECOLOGIA / OBSTETRICIA Año: 2019 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_doencas_nao_transmissiveis Asunto principal: Inmunoglobulinas / Infecciones por Citomegalovirus / Transmisión Vertical de Enfermedad Infecciosa / Citomegalovirus / Enfermedades Fetales Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Ultrasound Obstet Gynecol Asunto de la revista: DIAGNOSTICO POR IMAGEM / GINECOLOGIA / OBSTETRICIA Año: 2019 Tipo del documento: Article País de afiliación: Alemania
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