Key result
Maternal primary CMV infection in the first trimester of a subsequent pregnancy was associated with a 24-fold higher risk of cCMV (RR 24; 95% CI 10.8-62.3) than the general pregnant population.
Why the study?
Maternal parity is an established risk factor of cCMV in previously seronegative women, but the specific risk of cCMV and related sequelae following primary first-trimester infections in subsequent pregnancies required quantification.
Cohort (n=739)
No
Relative Risk: 24 (95% CI 10.8–62.3)
Women seronegative at their first pregnancy who have a subsequent pregnancy within 2 years are at a significantly increased risk of delivering a child with cCMV-related sequelae.
Short inter-pregnancy intervals may heighten cCMV sequelae risk after seronegative first pregnancy; leaves optimal screening open pending prospective data.
BACKGROUND: In women seronegative before pregnancy, congenital cytomegalovirus (cCMV)-related sequelae are exclusively seen in those infected in the first trimester of pregnancy. Following a maternal primary infection in the first trimester, up to 30% of infected neonates suffer long-term sequelae. Maternal parity is an established risk factor of cCMV in previously seronegative women. Our objective was to quantify, in a population of women seronegative at their first pregnancy, the risk of cCMV and related sequelae following primary infections in the first trimester in subsequent pregnancies. METHODS: There were 739 women seronegative at their first pregnancy who had at least 1 of 971 subsequent pregnancies and deliveries managed at our institution. All women had CMV immunoglobin (Ig) G and IgM testing at 11-14 weeks of each pregnancy. RESULTS: Between 2 consecutive pregnancies, 15.6% (115/739) of women seroconverted. Of these seroconversions, 29% (33/115) occurred in the periconceptional period or in the first trimester. The risks for cCMV and related sequelae (neurologic and/or hearing loss) following a maternal infection in the first trimester were, respectively, 24- and 6-fold higher (risk ratios, 24 [95% confidence interval {CI}, 10.8-62.3] and 6 [95% CI 1.5-24], respectively) than in the general pregnant population. Of all primary maternal infections and fetal infections in the first trimester, 88% (29/33) and 92% (11/12), respectively, occurred when the inter-pregnancy interval was ≤2 years. CONCLUSIONS: 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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Leruez‐Ville et al. (2019) conducted a cohort in Congenital cytomegalovirus (cCMV) infection (n=739). Maternal primary CMV infection in the first trimester vs. General pregnant population was evaluated on Congenital cytomegalovirus (cCMV) (RR 24, 95% CI 10.8-62.3). Maternal primary CMV infection in the first trimester of a subsequent pregnancy was associated with a 24-fold higher risk of cCMV (RR 24; 95% CI 10.8-62.3) than the general pregnant population.
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