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Congenital cytomegalovirus infection

Congenital cytomegalovirus infection


Congenital cytomegalovirus infection
Classification and external resources

Micrograph of a cytomegalovirus (CMV) infection of the placenta (CMV placentitis). The characteristic large nucleus of a CMV infected cell is
seen off-centre at the bottom-right of the image. H&E stain.
[1]

ICD-10

P35.1

ICD-9

771.1

MedlinePlus

001343

eMedicine

article/963090

[2]
[3]
[4]

Congenital cytomegalovirus infection refers to a condition where cytomegalovirus is transmitted in the perinatal
period.
HCMV is one of the TORCH infections that lead to congenital abnormalities. (These are: toxoplasmosis, rubella,
cytomegalovirus, and herpes simplex. )

Epidemiology
Congenital HCMV infection occurs when the mother suffers a primary infection (or reactivation) during pregnancy.
Due to the lower seroprevalence of HCMV in industrialized countries and higher socioeconomic groups, congenital
infections are actually less common in poorer communities, where more women of child-bearing age are already
seropositive. In industrialized countries up to 8% of HCMV seronegative mothers contract primary HCMV infection
during pregnancy, of which roughly 50% will transmit to the fetus. Between 22-38% of infected fetuses are then
born with symptoms, which may include pneumonia, gastrointestinal, retinal and neurological disease. HCMV
infection occurs in roughly 1% of all neonates with those who are not congenitally infected contracting the infection
possibly through breast milk. Other sources of neonatal infection are bodily fluids which are known to contain high
titres in shedding individuals: saliva (<107copies/ml) and urine (<105copies/ml ) seem common routes of
transmission.
The incidence of primary CMV infection in pregnant women in the United States varies from 1% to 3%. Healthy
pregnant women are not at special risk for disease from CMV infection. When infected with CMV, most women
have no symptoms and very few have a disease resembling infectious mononucleosis. It is their developing fetuses
that may be at risk for congenital CMV disease. CMV remains the most important cause of congenital viral infection
in the United States. HCMV is the most common cause of congenital infection in humans and intrauterine primary
infections are more common than other well-known infections and syndromes, including Down Syndrome, Fetal

Congenital cytomegalovirus infection


Alcohol Syndrome, Spina Bifida, and Pediatric HIV/AIDS.[5]

Presentation
For infants who are infected by their mothers before birth, two potential adverse scenarios exist:
Generalized infection may occur in the infant, and can cause complications such as low birth weight,
microcephaly, seizures, petechial rash similar to the "blueberry muffin" rash of congenital rubella syndrome, and
moderate hepatosplenomegaly (with jaundice). Though severe cases can be fatal, with supportive treatment most
infants with CMV disease will survive. However, from 80% to 90% will have complications within the first few
years of life that may include hearing loss, vision impairment, and varying degrees of mental retardation.
Another 5% to 10% of infants who are infected but without symptoms at birth will subsequently have varying
degrees of hearing and mental or coordination problems.
These risks appear to be almost exclusively associated with women who previously have not been infected with
CMV and who are having their first infection with the virus during pregnancy. There appears to be little risk of
CMV-related complications for women who have been infected at least 6 months prior to conception. For this group,
which makes up 50% to 80% of the women of child-bearing age, the rate of newborn CMV infection is 1%, and
these infants appear to have no significant illness or abnormalities.
The virus can also be transmitted to the infant at delivery from contact with genital secretions or later in infancy
through breast milk. However, these infections usually result in little or no clinical illness in the infant.
To summarise, during a pregnancy when a woman who has never had CMV infection becomes infected with CMV,
there is a risk that after birth the infant may have CMV-related complications, the most common of which are
associated with hearing loss, visual impairment, or diminished mental and motor capabilities. On the other hand,
infants and children who acquire CMV after birth have few, if any, symptoms or complications.

Prevention
Recommendations for pregnant women with regard to CMV infection:
Throughout the pregnancy, practice good personal hygiene, especially handwashing with soap and water, after
contact with diapers or oral secretions (particularly with a child who is in day care).
Women who develop a mononucleosis-like illness during pregnancy should be evaluated for CMV infection and
counseled about the possible risks to the unborn child.
Laboratory testing for antibody to CMV can be performed to determine if a woman has already had CMV
infection.
Recovery of CMV from the cervix or urine of women at or before the time of delivery does not warrant a
cesarean section.
The demonstrated benefits of breast-feeding outweigh the minimal risk of acquiring CMV from the breast-feeding
mother.
There is no need to either screen for CMV or exclude CMV-excreting children from schools or institutions
because the virus is frequently found in many healthy children and adults.

Childcare
Most healthy people working with infants and children face no special risk from CMV infection. However, for
women of child-bearing age who previously have not been infected with CMV, there is a potential risk to the
developing unborn child (the risk is described above in the Pregnancy section). Contact with children who are in day
care, where CMV infection is commonly transmitted among young children (particularly toddlers), may be a source
of exposure to CMV. Since CMV is transmitted through contact with infected body fluids, including urine and
saliva, child care providers (meaning day care workers, special education teachers, as well as mothers) should be

Congenital cytomegalovirus infection


educated about the risks of CMV infection and the precautions they can take. Day care workers appear to be at a
greater risk than hospital and other health care providers, and this may be due in part to the increased emphasis on
personal hygiene in the health care setting.
Recommendations for individuals providing care for infants and children:
Employees should be educated concerning CMV, its transmission, and hygienic practices, such as handwashing,
which minimize the risk of infection.
Susceptible nonpregnant women working with infants and children should not routinely be transferred to other
work situations.
Pregnant women working with infants and children should be informed of the risk of acquiring CMV infection
and the possible effects on the unborn child.
Routine laboratory testing for CMV antibody in female workers is not specifically recommended due to its high
occurrence, but can be performed to determine their immune status.

CMV Testing and Diagnosis


People infected with CMV develop antibodies to it, initially IgM later IgG indicating current infection and immunity
respectively. If the virus is detected in the blood, saliva, urine or other body tissues, it means that the person has an
active infection.
When infected with CMV, most women have no symptoms, but some may have symptoms resembling
mononucleosis. Women who develop a mononucleosis-like illness during pregnancy should consult their medical
provider.
The Centers for Disease Control and Prevention (CDC) does not recommend routine maternal screening for CMV
infection during pregnancy because there is no test that can definitively rule out primary CMV infection during
pregnancy. Women who are concerned about CMV infection during pregnancy should practice CMV prevention
measures.Considering that the CMV virus is present in saliva, urine, tears, blood, mucus, and other bodily fluids,
frequent hand washing with soap and water is important after contact with diapers or oral secretions, especially with
a child who is in daycare or interacting with other young children on a regular basis.
A diagnosis of congenital CMV infection can be made if the virus is found in an infant's urine, saliva, blood, or other
body tissues during the first week after birth. Antibody tests cannot be used to diagnose congenital CMV; a diagnosis
can only be made if the virus is detected during the first week of life. Congenital CMV cannot be diagnosed if the
infant is tested more than one week after birth.
Visually healthy infants are not routinely tested for CMV infection although only 10-20% will show signs of
infection at birth[citation needed] though up to 80% may go onto show signs of prenatal infection in later life. If a
pregnant woman finds out that she has become infected with CMV for the first time during her pregnancy, she
should have her infant tested for CMV as soon as possible after birth.

Congenital cytomegalovirus infection

References
[1]
[2]
[3]
[4]
[5]

http:/ / apps. who. int/ classifications/ icd10/ browse/ 2010/ en#/ P35. 1
http:/ / www. icd9data. com/ getICD9Code. ashx?icd9=771. 1
http:/ / www. nlm. nih. gov/ medlineplus/ ency/ article/ 001343. htm
http:/ / emedicine. medscape. com/ article/ 963090-overview
()

External links
Cytomegalovirus (CMV) (http://www.nhs.uk/conditions/Cytomegalovirus/) - NHS Choices
CMV: Congenital CMV Infection (http://www.cdc.gov/cmv/congenital-infection.html) - CDC

Article Sources and Contributors

Article Sources and Contributors


Congenital cytomegalovirus infection Source: http://en.wikipedia.org/w/index.php?oldid=593844694 Contributors: Arcadian, ArcadianOnUnsecuredLoc, Bearcat, Diptanshu.D, Download,
John of Reading, Klgillis, Lepidoptera, Ruslik0, Wolfmankurd, Xezbeth, 2 anonymous edits

Image Sources, Licenses and Contributors


File:CMV placentitis1 mini.jpg Source: http://en.wikipedia.org/w/index.php?title=File:CMV_placentitis1_mini.jpg License: Creative Commons Attribution-Sharealike 3.0 Contributors:
Nephron

License
Creative Commons Attribution-Share Alike 3.0
//creativecommons.org/licenses/by-sa/3.0/

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