[HTML][HTML] Primary human cytomegalovirus (HCMV) infection in pregnancy

H Buxmann, K Hamprecht… - Deutsches Ärzteblatt …, 2017 - ncbi.nlm.nih.gov
H Buxmann, K Hamprecht, M Meyer-Wittkopf, K Friese
Deutsches Ärzteblatt International, 2017ncbi.nlm.nih.gov
Background In 0.5–4% of pregnancies, the prospective mother sustains a primary infection
with human cytomegalovirus (HCMV). An HCMV infection of the fetus in the first or second
trimester can cause complex post-encephalitic impairment of the infant brain, leading to
motor and mental retardation, cerebral palsy, epilepsy, retinal defects, and progressive
hearing loss. Methods This review is based on pertinent publications from January 2000 to
October 2016 that were retrieved by a selective search in PubMed employing the terms …
Abstract
Background
In 0.5–4% of pregnancies, the prospective mother sustains a primary infection with human cytomegalovirus (HCMV). An HCMV infection of the fetus in the first or second trimester can cause complex post-encephalitic impairment of the infant brain, leading to motor and mental retardation, cerebral palsy, epilepsy, retinal defects, and progressive hearing loss.
Methods
This review is based on pertinent publications from January 2000 to October 2016 that were retrieved by a selective search in PubMed employing the terms “cytomegalovirus and pregnancy” and “congenital cytomegalovirus.”
Results
85–90% of all neonates with HCMV infection are asymptomatic at birth. The main long-term sequela is hearing impairment, which develops in 8–15% of these affected children. Hygienic measures can lower the risk of primary HCMV infection in pregnancy by 50–85%. The first randomized and controlled trial (RCT) of passive immunization with an HCMV-specific hyperimmune globulin (HIG) preparation revealed a trend toward a lower risk of congenital transmission of the virus (30% versus 44% with placebo, p= 0.13). The effect of HIG was more marked in the initial non-randomized trial (15% versus 40%, p= 0.02). The RCT also showed HIG to be associated with a higher frequency of fetal growth retardation and premature birth (13% versus 2%, p= 0.06). Valaciclovir is a further, non-approved treatment option.
Conclusion
In the absence of an active vaccine against HCMV, counseling about hygienic measures may currently be the single most effective way to prevent congenital HCMV infection. Moreover, HCMV serologic testing is recommended in the guideline of the Association of the Scientific Medical Societies in Germany (Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften, AWMF). Further randomized trials of treatment with HIG and with valaciclovir are urgently needed so that the options for the prevention and treatment of congenital HCMV infection can be assessed.
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