The World Health Organization has declared the Zika virus an international public health emergency, with a prediction of about
four million people being infected at the end of the year.
WHO has issued a travel warning for pregnant women advising
them not to travel to areas with continuing outbreaks of Zika virus due to the
potential risk of birth defects.
Sexual transmission appears to be more common than
previously thought of. "Pregnant women whose sexual partners live in or
travel to areas with Zika virus outbreaks should ensure safe sexual practices
or abstain from sex for the duration of their pregnancy," the WHO said,
based on advice from its Emergency Committee of independent experts.
According to a preliminary report of case series from Rio
de Janeiro, Brazil,
published online
March 4 issue of the New England Journal of Medicine, ZIKA is also
linked to fetal death, placental insufficiency, IUGR and Nervous system
malformation.
Dr. PatrĂcia Brasil, MD, the principal investigator of the
study “our findings provide further
support for a link between maternal ZIKV infection and fetal and placental
abnormalities that is not unlike that of other viruses that are known to cause
congenital infections characterized by intrauterine growth restriction and
placental insufficiency.”
In September, 2015 researchers in Brazil identified dengue like
fever, which was later identified as ZIKV. In the same month the ZIKV was
linked to microcepahy, cases in Brazil
rocketed to 3,500 from 147, the average for the same time last year (2014).
The link was first detected when Brazilian health
authorities found traces of the Zika virus in a deceased infant born with
microcephaly or in amniotic fluid of mothers delivering microcephalic infants.
In the present study, the researchers enrolled pregnant
women of any gestation, who presented with a rash that had developed within the
previous 5 days. Out of 88 women, 72 (82%) women tested positive ZIKV in blood
and/or urine by reverse-transcriptase polymerase chain reaction assays. The
researchers followed the women prospectively with clinical examinations and
serial ultrasound. All the study participants were generally healthy with no
h/o congenital malformations.
Clinically the women presented with a macular or maculopapular
rash, pruritus (94%) arthalgia (65%), conjuntival redness (58%). Fever was not
a significant symptom with only one third of women reporting it.
All the ZIKV negative as well as positive women had
ultrasound. USG showed abnormalities in 12 of ZIKV positive women while those
women who are negative showed normal USG.
Sonographically detected abnormalities include:
- intrauterine growth restriction, with or without accompanying microcephaly(5)
- cerebral calcification (4)
- CNS alterations (n = 2)
- Oligohydramnios and anhydramnios (2)
- Abnormal arterial flow in the cerebral or umbilical arteries(4)
- additional malformations, including agenesis of the vermis, Blake’s pouch cyst, and potentially a club foot, in addition to cerebral calcifications, intrauterine growth restriction, and microcephaly(1)
Abnormalities were present in fetuses of women irrespective
of there gestational age at ZIKV infection, although those women infected in
first trimester show signs of insult during embryogenesis. CNS abnormalities
seen in fetuses infected as late as 27 weeks.
Six live births and two still births occurred during the
follow up and confirmed the Sonography findings.
The authors suggest that “many aspects of ZIKV infection are
similar to those of rubella, particularly rash, arthralgias, pruritus, and
lymphadenopathy in the mother without high fever.” But, it is worrisome that
there is no population immunity for ZIKV as compared to rubella U.S.
pandemic of 1959–1965, when only 17.5% of women of childbearing age lacked
rubella antibodies.
In summary the study findings provide support to the
hypothesis of link between maternal ZIKV infection and fetal and placental
abnormalities. The women infected with ZIKV should be followed up closely with
serial ultrasonography to evaluate for signs of placental insufficiency, given
the risks of fetal death and intrauterine growth restriction.
References:
http://www.nejm.org/doi/full/10.1056/NEJMoa1602412?query=featured_home#t=articleDiscussion
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