Diagnosis of and screening for cytomegalovirus infection in pregnant women

被引:133
作者
Munro, SC
Hall, B
Whybin, LR
Leader, L
Robertsons, P
Maine, GT
Rawlinson, WD
机构
[1] Prince Wales Hosp, Div Virol, Dept Microbiol, SEALS, Randwick, NSW 2031, Australia
[2] Prince Wales Hosp, Serol Lab, Dept Microbiol, SEALS, Randwick, NSW 2031, Australia
[3] Univ New S Wales, Sch Biotechnol & Biomol Sci, Kensington, NSW 2033, Australia
[4] Univ New S Wales, Sch Med Sci, Kensington, NSW 2033, Australia
[5] Royal Hosp Women, Randwick, NSW, Australia
[6] Abbott Labs, Div Diagnost, Core Res & Dev, Abbott Pk, IL 60064 USA
关键词
D O I
10.1128/JCM.43.9.4713-4718.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
No single diagnostic test for cytomegalovirus (CMV) infection is currently available for pregnant women at all stages of gestation. Improved accuracy in estimating the timing of primary infections can be used to identify women at higher risk of giving birth to congenitally infected infants. A diagnostic algorithm utilizing immunoglobulin G (IgG), IgM, and IgG avidity was used to prospectively screen serum from 600 pregnant women enrolled from two groups: <= 20 weeks gestation (n = 396) or > 20 weeks gestation (n = 204). PCR testing of urine and/or blood was performed on all seropositive women (n = 341). The majority (56.8%) of women were CMV IgG seropositive, with 5.5% being also CMV IgM positive. In the IgM-positive women, 1.2% had a low-avidity IgG, indicating a primary CMV infection and a high risk of intrauterine transmission. Two infants with asymptomatic CMV infection were born of mothers who had seroconverted in the second trimester of pregnancy. Baseline, age-stratified CMV serostatus was established from 1,018 blood donors. Baseline seropositivity from a blood donor population increased with age from 34.9% seroprevalence at less than 20 years of age to 72% seroprevalence at 50 years of age. Women at high risk of intrauterine transmission of CMV were identified at all stages of gestation. Women infected with CMV during late gestation may be more likely to transmit the virus, so failure to detect seroconversions in late gestation may result in failure to detect infected neonates.
引用
收藏
页码:4713 / 4718
页数:6
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