首次妊娠时血清阴性的妇女在随后妊娠中先天性巨细胞病毒感染(cCMV)的长期后遗症的量化负担

M. Leruez-Ville, T. Guilleminot, J. Stirnemann, L. Salomon, E. Spaggiari, V. Faure-Bardon, J. Magny, Y. Ville
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All women had CMV IgG and IgM testing at 11-14 weeks' of each pregnancy.\n\n\nRESULTS\n15.6% (115/739) of women seroconverted between 2 consecutive pregnancies. 29% (33/115) of seroconversions occurred in the periconceptional period or in the first trimester. The risks for cCMV and related sequelae (neurologic and/or hearing loss) following maternal infection in the first trimester were respectively 24 and 6-fold higher (RR [95%CI] =24 [10.8-62.3] and 6 [1.5-24]) than the general pregnant population. 88% (29/33) and 92% (11/12) of, respectively, all primary maternal infections and fetal infections in the 1st trimester occurred when the inter-pregnancy interval was ≤2 years.\n\n\nCONCLUSION\nWomen seronegative at their first pregnancy with a subsequent pregnancy within 2 years have the highest risk of delivering a child with cCMV-related sequelae. 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引用次数: 21

摘要

在孕前血清阴性的妇女中,cCMV相关的后遗症仅见于妊娠前三个月感染的妇女。在妊娠早期,多达30%的受感染新生儿在母体初次感染后会出现长期后遗症。在以前血清阴性的妇女中,产妇产次是cCMV的一个确定的危险因素。目的量化首次妊娠血清阴性妇女妊娠早期感染cCMV及相关后遗症的风险。方法739例首次妊娠血清阴性的妇女,在我院管理的971例妊娠和分娩中至少有一例。结果15.6%(115/739)的妇女在连续两次妊娠期间血清转化。29%(33/115)的血清转换发生在妊娠期或妊娠早期。妊娠前三个月母体感染cCMV及相关后遗症(神经和/或听力损失)的风险分别是一般妊娠人群的24倍和6倍(RR [95%CI] =24[10.8-62.3]和6[1.5-24])。88%(29/33)和92%(11/12)的孕妇在妊娠早期感染发生在妊娠间隔≤2年。结论首次妊娠血清阴性且2年内再次妊娠的妇女,其分娩时伴有ccv相关后遗症的风险最高。应该让这些妇女意识到这种风险,并在妊娠早期给予血清学筛查的机会。
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Quantifying the burden of congenital CMV infection (cCMV) with long-term sequelae in subsequent pregnancies of women seronegative at their first pregnancy.
BACKGROUND In women seronegative before pregnancy, cCMV related sequelae are exclusively seen in those infected in the first trimester of pregnancy. Up to 30% of infected neonates following maternal primary infection in the first trimester suffer long-term sequelae. Maternal parity is an established risk factor of cCMV in previously seronegative women. OBJECTIVE to quantify the risk of cCMV and related sequelae following primary infection in the first trimester in subsequent pregnancies in a population of women seronegative at their first pregnancy. METHODS 739 women seronegative at their first pregnancy had at least one of 971 subsequent pregnancies and deliveries managed at our institution. All women had CMV IgG and IgM testing at 11-14 weeks' of each pregnancy. RESULTS 15.6% (115/739) of women seroconverted between 2 consecutive pregnancies. 29% (33/115) of seroconversions occurred in the periconceptional period or in the first trimester. The risks for cCMV and related sequelae (neurologic and/or hearing loss) following maternal infection in the first trimester were respectively 24 and 6-fold higher (RR [95%CI] =24 [10.8-62.3] and 6 [1.5-24]) than the general pregnant population. 88% (29/33) and 92% (11/12) of, respectively, all primary maternal infections and fetal infections in the 1st trimester occurred when the inter-pregnancy interval was ≤2 years. CONCLUSION Women seronegative at their first pregnancy with a subsequent pregnancy within 2 years have the highest risk of delivering a child with cCMV-related sequelae. These women should be made aware of the risk and given the opportunity of serology screening in the first trimester.
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