Congenital CMV Infection Blood Test

What is Congenital Cytomegalovirus (CMV) Infection?

Congenital cytomegalovirus (CMV) infection is a viral infection present at birth that occurs when a baby is infected with CMV before birth through transmission from the mother during pregnancy. It is caused by the cytomegalovirus crossing the placenta during maternal primary infection or reactivation of a previous CMV infection. The Cytomegalovirus (CMV) Antibodies, IgM, Quantitative test is the most important test for diagnosis because it detects IgM antibodies indicating recent or active infection in the newborn.

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What causes congenital CMV infection?

Congenital CMV infection is caused by the cytomegalovirus (CMV) crossing the placenta from an infected mother to her developing baby during pregnancy. This transmission can happen when a pregnant woman experiences a primary CMV infection for the first time or when a previous CMV infection reactivates during pregnancy. The virus can be transmitted at any stage of pregnancy, though the risk and severity of complications may vary depending on when during pregnancy the transmission occurs.

What is the best test for congenital CMV infection?

The Cytomegalovirus (CMV) Antibodies, IgM, Quantitative test is the most important test for congenital CMV infection because it detects IgM antibodies that indicate a recent or active CMV infection in the newborn. IgM antibodies are the first immune response produced when the body encounters CMV, and their presence in a newborn's blood strongly suggests that the baby was infected during pregnancy. This quantitative test measures specific levels of these antibodies, helping doctors assess both the likelihood of infection and its potential severity, which guides decisions about monitoring and treatment.

When should I get tested for congenital CMV infection?

You should get tested if you are pregnant and have symptoms of CMV infection such as fever, fatigue, sore throat, or swollen glands, or if you have been exposed to someone with CMV. Testing is also recommended for newborns who show signs of congenital infection at birth, including small head size, jaundice, enlarged liver or spleen, purple skin spots, or seizures. Additionally, babies who appear healthy at birth but fail newborn hearing screenings should be tested, as hearing loss is one of the most common complications of congenital CMV infection that may not be immediately apparent.

What are the symptoms of congenital CMV infection?
Most babies with congenital CMV infection appear healthy at birth and show no immediate symptoms, but about 10-20% are born with signs of the infection. Symptomatic newborns may have a small head size (microcephaly), premature birth, low birth weight, jaundice, enlarged liver and spleen, purple skin spots or rashes, seizures, or feeding difficulties. Even babies who seem healthy at birth can develop complications later, including hearing loss, vision problems, developmental delays, intellectual disabilities, or coordination problems, which is why monitoring is important.
Who is at risk for congenital CMV infection?
Babies are at risk for congenital CMV infection when their mothers become infected with CMV for the first time during pregnancy or experience reactivation of a dormant CMV infection while pregnant. Pregnant women who work with young children, such as daycare workers or preschool teachers, face higher risk because CMV spreads easily among young children through saliva and urine. Women with weakened immune systems or those who have other children at home, particularly toddlers in daycare, are also at increased risk of contracting CMV during pregnancy.
What happens if congenital CMV infection is left untreated?
Untreated congenital CMV infection can lead to serious long-term complications that may worsen over time. The most common complication is progressive hearing loss, which can occur even in children who appeared healthy at birth and may not develop until months or years later. Other potential complications include vision problems or blindness, intellectual disabilities, developmental delays, seizures, coordination problems, and learning difficulties. Early detection through testing allows for antiviral treatment in severe cases and enables doctors to monitor children closely for these complications so interventions can begin as soon as problems are detected.
Can congenital CMV infection be diagnosed with a blood test?
Yes, congenital CMV infection can be diagnosed with blood tests that detect antibodies the body produces in response to the virus. The CMV IgM antibody test is particularly useful because IgM antibodies appear first when someone is newly infected, making them a good indicator of recent infection in newborns. For the most accurate diagnosis of congenital CMV, testing should be done within the first three weeks of life, as this confirms the baby was infected before birth rather than after delivery. Blood tests may be combined with urine or saliva tests for comprehensive diagnosis.
How is congenital CMV infection treated?
Babies with symptomatic congenital CMV infection may be treated with antiviral medications such as ganciclovir or valganciclovir, which can help reduce the severity of complications, particularly hearing loss and developmental problems. Treatment typically lasts for six months and is most effective when started early in infancy. Even if antiviral treatment is not used, all babies diagnosed with congenital CMV require ongoing monitoring, including regular hearing tests, vision checks, and developmental assessments throughout childhood. Supportive therapies such as hearing aids, speech therapy, physical therapy, and early intervention programs can help children reach their full potential.
How can I prevent congenital CMV infection?
Pregnant women can reduce their risk of CMV infection by practicing good hygiene, especially if they have young children or work with children. Wash your hands thoroughly with soap and water for 15-20 seconds after changing diapers, feeding young children, wiping noses or drool, or handling children's toys. Avoid sharing food, drinks, eating utensils, toothbrushes, or towels with young children, and avoid putting a child's pacifier in your mouth. Do not kiss young children on the mouth or cheek; instead kiss them on the head or give hugs. These simple precautions can significantly reduce the risk of CMV transmission during pregnancy.
What can I do at home for congenital CMV infection?
While congenital CMV infection requires medical supervision and cannot be cured with home remedies, you can support your baby's health and development at home with proper care. Ensure your baby attends all scheduled medical appointments and hearing screenings, as early detection of problems allows for prompt intervention. If your child is receiving therapies such as speech, physical, or occupational therapy, practice the recommended exercises and activities at home consistently. Maintain good nutrition, adequate sleep, and a stimulating environment with age-appropriate activities to support optimal development. Stay connected with your healthcare team and early intervention services to address any emerging concerns quickly.
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Cytomegalovirus (CMV) Antibodies, IgM, Quantitative
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