Neonatal herpes affects about 1 in 15,000 newborns and the prognosis for di
sseminated disease with encephalitis is poor. We investigated whether acycl
ovir prophylaxis in late pregnancy effectively reduces the risk of viral sh
edding and. hence, of mother-to-child transmission at delivery.
A prospective study was conducted. Pregnant women who had at least one epis
ode of genital herpes during pregnancy were randomly assigned to two groups
: group 1 (n=167) received oral acyclovir from 36 weeks of gestation to ter
m, group 2 (n=121) received no treatment. Group 3 (n=201) comprised women n
ot given prophylaxis who had a history of genital herpes. but no active epi
sodes during pregnancy. No specific instruction were set up for obstetrical
management except For cesarean section in case of a suspected herpes lesio
n at the time of labor.
The rate of Cesarean section was 8.3% in group 1, 16.54 in group 3, and 9.9
% in group 3 (p<0.001). 75% of cesareans in group 2 and 10% in group 3 were
done for genital herpes. Percentage of viral shedding was, respectively. 0
% (group 1), 5% (group 2), and 0.5% (group 3) (p<0.05).
These findings underline the value of antiviral prophylaxis in late pregnan
cy for women with a known history of genital herpes. Such prophylaxis only
partly prevents neonatal herpes infection, because it is not applicable: to
patients with no known clinical history but may excrete the virus. (C) 200
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