Ms H Begum,
aged 29 yrs , primigravida , carrying 15 weeks of gestation with normal NT scan and Double marker reports had an attack of a Varicella zoster on 01-07-20
is worried about foetal abnormalities . Her husband has since gone to another country
on contractual basis and can’t come home in next seven yrs. She is worried about teratogenecity and reluctant
to simply go ahead with MTP based on theoretical or should I say presumptive possibility
of cong abnormalities. My Q to members can we offer any diag tests to confirm that
fetus in question is really affected? If so what are those tests that I shall advise
her enabling her and myself that there is almost certainly foetal affection?? After
how many weeks of acute varicella such targeted scan can be imaged?? Additionally
should we enquire about varicella vaccine
routinely to all women planning for pregancy or insist on some Lab tests to confirm presence of
antibodies in case she don’t remember details of childhood vaccination??
When to do USG to pick
up varicella induced changes?? Timing of
USG?? Ans: A time
lag of at least 5 weeks after the primary infection is advised because
ultrasound performed at 4 weeks has failed to detect the deformities.
Associated sonographic features of polyhydramnios fetal hydrops may add to
specific findings in aiding diagnosis.
What about foetal MRI??
Fetal magnetic resonance imaging
can be useful to look for morphological abnormalities . Yet , ultrasound
remains the best diagnostic modality to follow serially fetuses suspected or
known to have varicella infection.
What to look for?? There is no definitive method but targeted ultrasound for 1) limb deformity 2) microcephaly 3 ) hydrocephalus 4) gastrointestinal
and 5) genitourinary abnormalities ,6) cortical atrophy 7) soft tissue
calcification and 8) intrauterine growth restriction may be a method to assess the severity of
infection.
Long term ill health: - This syndrome is manifest by : Dermatomal scarring , Limb hypoplasia, ocular
abnormalities , Low birth weight , cortical atrophy and mental retardation , early
infant death .
What is role of amniocentesis
in this case ? Ans: VZV DNA can be detected by polymerase chain or culture in amniotic
fluid. VZV DNA has a high sensitivity but a low
specificity for the development of CVS(cong varicella syndrome)
Why don’t usually don’t embark
on amniocentesis so liberally? Ans: Stratification of risk in this case is very relevant. Amniocentesis is not routinely advised because
the risk of CVS(cong varicella syndrome) is low even in the presence of positive VZV
DNA in the amniotic fluid. If amniotic fluid is PCR positive for VZV and the
ultrasound is normal at 17-21 weeks the risk of CVS is low. Serial follow up
ultrasound are therefore advised and if repeat ultrasound is normal at 23-24
weeks the risk of CVS is remote. The risk of CVS(cong varicella syndrome) is very high if the ultrasound shows features
compatible with CVS and the amniotic fluid is positive. A negative result in
amniotic fluid and a normal ultrasound from 23 weeks onwards suggest a low risk
of intrauterine infection.
What about Cordocentesis in this case ?? Fetal bold sampling for varicella specific IgM
antibody is not useful. While total IgM concentration may be elevated in
setting of acute viral infection the detection of antibody in the fetal compartment does not indicate
the severity of fetal infection.
Prevalence
of foetal infection: - The incidence of CVS has been previously reported to be as high as 2%
when maternal infection occurs between 13 and 20 weeks gestation. A more recent
pooled estimate from cohort studies suggests a rate of 1.4% in the second
trimester and 0.55% in the first trimester . Virtually all cases occur in the first 20 weeks of
gestation with the overall rate in this period being 0.91% .
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