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

被引:15
作者
Chatzakis, C. [1 ]
Sotiriadis, A. [1 ]
Dinas, K. [1 ]
Ville, Y. [2 ,3 ,4 ]
机构
[1] Aristotle Univ Thessaloniki, Fac Med, Dept Obstet & Gynaecol 2, Thessaloniki, Greece
[2] Univ Paris, Paris Descartes Univ, EA Fetus, Paris, France
[3] Necker Enfants Malad Hosp, AP HP, Dept Obstet Fetal Med & Surg, Paris, France
[4] Univ Paris, AP HP, F-75005 Paris, France
关键词
amniocentesis; CMV; congenital cytomegalovirus infection; cytomegalovirus; meta-analysis; sequelae; PRENATAL-DIAGNOSIS; PREGNANCIES;
D O I
10.1002/uog.26128
中图分类号
O42 [声学];
学科分类号
070206 ; 082403 ;
摘要
ObjectiveCytomegalovirus (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. MethodsObservational 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%; I2 = 0%) in fetuses with a negative amniocentesis result and 22.0% (95% CI, 11.0-38.0%; I2 = 75%) in those with a positive amniocentesis result. The pooled odds ratio (OR) was 0.03 (95% CI, 0.01-0.10; I2 = 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%; I2 = 0%) and, in those with a positive amniocentesis result, it was 14.0% (95% CI, 7.0-26.0%; I2 = 64%). The pooled OR was 0.04 (95% CI, 0.01-0.14; I2 = 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%; I2 = 0%) in fetuses with a negative amniocentesis result and 20.0% (95% CI, 10.0-36.0%; I2 = 82%) in those with a positive amniocentesis result. The pooled OR was 0.03 (95% CI, 0.01-0.08; I2 = 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. ConclusionA 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. (c) 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
引用
收藏
页码:158 / 167
页数:10
相关论文
共 24 条
[1]  
[Anonymous], 2014, NEWCASTLE OTTAWA SCA, DOI DOI 10.1007/S10654-010-9491-Z
[2]   Prenatal diagnosis of congenital cytomegalovirus infection [J].
Azam, AZ ;
Vial, Y ;
Fawer, CL ;
Zufferey, J ;
Hohlfeld, P .
OBSTETRICS AND GYNECOLOGY, 2001, 97 (03) :443-448
[3]   Clinical Implications for Children Born With Congenital Cytomegalovirus Infection Following a Negative Amniocentesis [J].
Bilavsky, Efraim ;
Pardo, Joseph ;
Attias, Joseph ;
Levy, Itzhak ;
Magny, Jean-Francois ;
Ville, Yves ;
Leruez-Ville, Marianne ;
Amir, Jacob .
CLINICAL INFECTIOUS DISEASES, 2016, 63 (01) :33-38
[4]   Washing our hands of the congenital cytomegalovirus disease epidemic [J].
Cannon, MJ ;
Davis, KF .
BMC PUBLIC HEALTH, 2005, 5 (1)
[5]   Timing of primary maternal cytomegalovirus infection and rates of vertical transmission and fetal consequences [J].
Chatzakis, Christos ;
Ville, Yves ;
Makrydimas, George ;
Dinas, Konstantinos ;
Zavlanos, Apostolos ;
Sotiriadis, Alexandros .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2020, 223 (06) :870-+
[6]   Prenatal diagnosis of congenital cytomegalovirus infection in 189 pregnancies with known outcome [J].
Enders, G ;
Bäder, U ;
Lindemann, L ;
Schalasta, G ;
Daiminger, A .
PRENATAL DIAGNOSIS, 2001, 21 (05) :362-377
[7]   First-trimester diagnosis of congenital cytomegalovirus infection after maternal primary infection in early pregnancy: feasibility study of viral genome amplification by PCR on chorionic villi obtained by CVS [J].
Faure-Bardon, V ;
Fourgeaud, J. ;
Guilleminot, T. ;
Magny, J-F ;
Salomon, L. J. ;
Bernard, J-P ;
Leruez-Ville, M. ;
Ville, Y. .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2021, 57 (04) :568-572
[8]   Human cytomegalovirus infection of placental cytotrophoblasts in vitro and in utero: Implications for transmission and pathogenesis [J].
Fisher, S ;
Genbacev, O ;
Maidji, E ;
Pereira, L .
JOURNAL OF VIROLOGY, 2000, 74 (15) :6808-6820
[9]   MATERNAL AGE AND CONGENITAL CYTOMEGALOVIRUS-INFECTION - SCREENING OF 2 DIVERSE NEWBORN POPULATIONS, 1980-1990 [J].
FOWLER, KB ;
STAGNO, S ;
PASS, RF .
JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (03) :552-556
[10]   Congenital cytomegalovirus infection following antenatal negative diagnostic amniotic fluid analysis - A single center experience [J].
Gabbay-Ben Ziv, Rinat ;
Yogev, Yariv ;
Peled, Yoav ;
Amir, Jacob ;
Pardo, Joseph .
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2012, 25 (09) :1787-1790