Evidence map›Paper›PMID 40890649›Full record

ArticleBMC pregnancy and childbirth2025

Clinical characteristics, pregnancy outcomes, and neonatal effects of cytomegalovirus infection in pregnant women in Liuzhou city, North central Guangxi of Southern China: a retrospective study from 2018 to 2024.

Ling Zhang, Weiyou Lv, Jiaolian Ya, Yuanxiu Li, Dejian Yuan, Pengfei Cai, Lizhu Chen, Ning Tang, Hui Chen, Bailing Liu and 6 more

Abstract read
In one paragraph

Article in BMC pregnancy and childbirth, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Ling Zhang *Department of Medical Genetics, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Weiyou Lv *Department of Medical Reproductive Center, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Jiaolian YaLiuzhou Key Laboratory of Birth Defects Prevention and Control, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, 545000, Guangxi, China.
Yuanxiu LiDepartment of Medical Genetics, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Dejian YuanDepartment of Medical Genetics, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Pengfei CaiDepartment of Medical Genetics, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Lizhu ChenDepartment of Medical Genetics, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Ning TangComprehensive Experimental Center, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Hui ChenDepartment of Perinatal Health Clinic, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Bailing LiuDepartment of Perinatal Health Clinic, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, 545000, Guangxi, China.
Xiangrong TangDepartment of Otolaryngology, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, 545000, Guangxi, China.
Qiurong LaiDepartment of Ultrasound, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Guang ChengDepartment of Imaging, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Lifang ZhangComprehensive Experimental Center, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China.
Xiaoni Wei *Department of Medical Genetics, Liuzhou Hospital of Guangzhou Women and Children's Medical Center, Liuzhou, 545000, Guangxi, China. 13978083524@163.com.
Qingyan Zhong *Liuzhou Key Laboratory of Birth Defects Prevention and Control, Liuzhou Maternity and Child Healthcare Hospital, Liuzhou, 545000, Guangxi, China. 272509222@qq.com.

Funding

Innovative Research Group Project of the National Natural Science Foundation of China 82460332Natural Science Foundation of Guangxi Zhuang Autonomous Region 2024GXNSFAA010195Self-funded Scientific Research Project of Health Commission of Guangxi Zhuang Autonomous Region of China Z-B20232036The Guangxi Key Research and Development Program GuIKE AB25069054
6 · The paper itself

Abstract

objectiveTo evaluate the clinical characteristics, pregnancy and neonatal outcomes of cytomegalovirus (CMV) infection in pregnant women.

methodsThis retrospective study included 22,673 pregnant women from Liuzhou, Guangxi, China, between 2018 and 2024. Amniotic fluid samples collected during mid-to-late pregnancy were tested for CMV DNA. Clinical data among CMV-infected pregnant women were collected, including prenatal diagnosis indicators, early-pregnancy CMV antibodies, pregnancy and neonatal outcomes, and offspring follow-up outcomes.

resultsAmong 22,673 pregnant women, 36 (1.59‰) were tested positive for CMV DNA in amniotic fluid, among which 14 (38.9%) with adverse pregnancy outcomes, including 7(19.4%) termination of pregnancy, 3(8.3%) stillbirth and 4 (11.1%) preterm delivery. Prenatal imaging modalities detected fetal abnormalities 21 (58.3%) in the CMV-infected pregnant women, mainly were ventriculomegaly, fetal growth restriction (FGR), pericardial effusion, ascites, cardiomegaly, placentomegaly, enlarged cisterna magna and hyperechogenic bowel. Notably, Fetuses of 2 pregnant women with primary CMV infection developed severe edema. Four newborns failed with initial hearing screening during postnatal evaluation. Among them, two (50%) were diagnosed with severe sensorineural hearing loss (SNHL) and one child was diagnosed with cerebral palsy in subsequent clinical assessments.

conclusionDiagnosis of primary CMV infection during pregnancy is of critical importance. Current guidelines recommend implementing CMV serological screening during the first trimester, with subsequent CMV IgG avidity testing when CMV IgG antibodies are detected. Maternal CMV infection during the second and third trimesters may lead to fetal complications, including ventriculomegaly, FGR and fetal hydrops. Congenital CMV (cCMV) infection predominantly manifests with sensorineural hearing loss (SNHL) and cerebral palsy. It is essential to screen all neonates from CMV-infected pregnant women for CMV DNA and provide mandatory 5-year follow-up for symptomatic cCMV children.

Indexed as

Cytomegalovirus InfectionsPregnancy Complications, InfectiousPregnancy OutcomeAdultAmniotic FluidChinaCytomegalovirusDNA, ViralFemaleHumansInfant, NewbornPregnancyPremature BirthRetrospective StudiesDNA, ViralCMV IgGCMV IgMCMV PCRCongenital cytomegalovirus infectionNewbornPregnancySensorineural hearing loss (SNHL)

Identifiers

PMID40890649
PMCPMC12400692

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.