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Tytuł pozycji:

Neonatal and long-term outcomes of infants with congenital cytomegalovirus infection and negative amniocentesis: systematic review and meta-analysis.

Tytuł:
Neonatal and long-term outcomes of infants with congenital cytomegalovirus infection and negative amniocentesis: systematic review and meta-analysis.
Autorzy:
Chatzakis C; Second Department of Obstetrics and Gynaecology, Faculty of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Sotiriadis A; Second Department of Obstetrics and Gynaecology, Faculty of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Dinas K; Second Department of Obstetrics and Gynaecology, Faculty of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Ville Y; EA Fetus, Paris Descartes University, University of Paris, Paris, France.; Department of Obstetrics, Fetal Medicine and Surgery, Necker-Enfants Malades Hospital, AP-HP, Paris, France.
Źródło:
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology [Ultrasound Obstet Gynecol] 2023 Feb; Vol. 61 (2), pp. 158-167.
Typ publikacji:
Meta-Analysis; Systematic Review; Journal Article; Review
Język:
English
Imprint Name(s):
Publication: 2003- : Chichester, West Sussex, UK : John Wiley & Sons, Ltd.
Original Publication: Carnforth, Lancs, UK ; Park Ridge, N.J., USA : Parthenon Pub., c1991-
MeSH Terms:
Pregnancy Complications, Infectious*/epidemiology
Cytomegalovirus Infections*
Infant, Newborn ; Child ; Pregnancy ; Infant ; Female ; Humans ; Amniocentesis/methods ; Prospective Studies ; Cytomegalovirus ; Infectious Disease Transmission, Vertical ; Observational Studies as Topic
References:
Clin Infect Dis. 2016 Jul 1;63(1):33-8. (PMID: 27114380)
Am J Obstet Gynecol. 2016 Oct;215(4):462.e1-462.e10. (PMID: 27083761)
Am J Obstet Gynecol. 2020 Sep;223(3):330-349. (PMID: 32105678)
Clin Infect Dis. 2016 Jul 1;63(1):39-40. (PMID: 27114377)
BMC Public Health. 2005 Jun 20;5:70. (PMID: 15967030)
Clin Infect Dis. 2023 Feb 8;76(3):513-520. (PMID: 35717635)
Rev Med Virol. 2007 Jul-Aug;17(4):253-76. (PMID: 17579921)
Obstet Gynecol. 2001 Mar;97(3):443-8. (PMID: 11239654)
Obstet Gynecol. 1997 May;89(5 Pt 1):763-7. (PMID: 9166317)
J Virol. 2000 Aug;74(15):6808-20. (PMID: 10888620)
Am J Obstet Gynecol. 2000 Aug;183(2):476-82. (PMID: 10942490)
Am J Obstet Gynecol. 2020 Dec;223(6):870-883.e11. (PMID: 32460972)
J Matern Fetal Neonatal Med. 2012 Sep;25(9):1787-90. (PMID: 22489602)
Prenat Diagn. 2020 Dec;40(13):1671-1680. (PMID: 32459019)
J Infect Dis. 2008 Feb 15;197(4):593-6. (PMID: 18275277)
Ultrasound Obstet Gynecol. 2021 Apr;57(4):568-572. (PMID: 33533526)
Ultrasound Obstet Gynecol. 2020 Jul;56(1):128-151. (PMID: 32400006)
J Infect Dis. 1993 Sep;168(3):552-6. (PMID: 8394857)
J Clin Virol. 2006 Feb;35(2):210-5. (PMID: 16386950)
Prenat Diagn. 2013 Aug;33(8):751-8. (PMID: 23553686)
Prenat Diagn. 2001 May;21(5):362-77. (PMID: 11360277)
Obstet Gynecol. 2000 Jun;95(6 Pt 1):881-8. (PMID: 10831985)
Contributed Indexing:
Keywords: CMV; amniocentesis; congenital cytomegalovirus infection; cytomegalovirus; meta-analysis; sequelae
Entry Date(s):
Date Created: 20221122 Date Completed: 20230202 Latest Revision: 20230526
Update Code:
20240104
PubMed Central ID:
PMC10107880
DOI:
10.1002/uog.26128
PMID:
36412976
Czasopismo naukowe
Objective: Cytomegalovirus (CMV) DNA is detectable in the amniotic fluid collected by amniocentesis in cases in which the fetus has been infected. However, cases of congenital neonatal CMV infection with a negative amniocentesis result have also been reported in the literature. The aim of the present study was to compare pregnancies with a negative amniocentesis result to those with a positive amniocentesis result in terms of incidence of fetal insult and long-term sequelae.
Methods: Observational studies that included pregnant women with CMV infection who underwent amniocentesis and that reported their results together with neonatal and/or long-term outcomes of the offspring were included. The risk of bias in included studies was assessed using the Newcastle-Ottawa Scale. The rate of severe symptoms at birth, defined as neurological symptoms or multiorgan involvement at birth, and the rate of severe sensorineural hearing loss (SNHL) and/or neurodevelopmental impairment at follow-up were the main outcomes of the study. The secondary outcome was the rate of pregnancy termination due to the presence of CMV-associated central nervous system (CNS) findings or multiorgan involvement on ultrasound/magnetic resonance imaging (MRI).
Results: Seven studies were included in the systematic review and meta-analysis. The pooled false-negative rate of amniocentesis was 8.0% (95% CI, 5.0-13.0%). The pooled rate of severe symptoms at birth was 0.0% (95% CI, 0.0-1.0%; I 2  = 0%) in fetuses with a negative amniocentesis result and 22.0% (95% CI, 11.0-38.0%; I 2  = 75%) in those with a positive amniocentesis result. The pooled odds ratio (OR) was 0.03 (95% CI, 0.01-0.10; I 2  = 0%). The pooled rate of severe SNHL and/or neurodevelopmental impairment at follow-up in fetuses with a negative amniocentesis result was 0.0% (95% CI, 0.0-1.0%; I 2  = 0%) and, in those with a positive amniocentesis result, it was 14.0% (95% CI, 7.0-26.0%; I 2  = 64%). The pooled OR was 0.04 (95% CI, 0.01-0.14; I 2  = 0%). The pooled rate of pregnancy termination due to the presence of CMV-associated CNS findings or multiorgan involvement on ultrasound/MRI was 0.0% (95% CI, 0.0-2.0%; I 2  = 0%) in fetuses with a negative amniocentesis result and 20.0% (95% CI, 10.0-36.0%; I 2  = 82%) in those with a positive amniocentesis result. The pooled OR was 0.03 (95% CI, 0.01-0.08; I 2  = 0%). A subgroup analysis including only pregnancies with primary CMV infection and a sensitivity analysis including only prospective studies were carried out, showing very similar results to those of the main analysis.
Conclusion: A negative amniocentesis result in pregnant women with CMV infection ensures lack of fetal insult and long-term sequelae to the child, even if transmission has occurred. © 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
(© 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.)

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