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Cytomegalovirus (CMV) IgG Avidity

CPT

86644

Test Details

Methodology

ELISA

Result Turnaround Time

5 days

Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

Related Documents

Use

The intended use of this test is to determine the avidity of CMV IgG antibody in patients known to be positive for CMV IgG antibody.

IgG avidity testing is used to support the diagnosis of recent primary Cytomegalovirus (CMV) infection during pregnancy. In addition, discrimination between recent (primary) and past CMV infection can be an important tool in the clinical management of transplant recipients. Maternal infections by Cytomegalovirus can cause severe complications to the fetus or congenital abnormalities. As a rule, the risk of maternal transmission is critically related to the time of infection; hence, it is important to determine the timing of infection in pregnant individuals. Cytomegalovirus (CMV) can cause central nervous system damage in the fetus and can lead to long-term sequelae, including sensorineural hearing loss and chorioretinitis, respectively. Since the risk to the fetus is critically related to the time of infection, it is essential to accurately determine whether a pregnant person has acquired a primary infection of CMV during gestation or earlier.

IgG avidity assays measure the binding strength between IgG antibodies and pathogen that can help distinguish a primary infection from a past infection. Following primary CMV infection, IgG antibodies have low binding strength (low avidity) then over 2-4 months mature to high binding strength (high avidity).

Special Instructions

This assay currently is not available in New York state.

Limitations

This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.

Specimen Requirements

Specimen

Serum

Volume

1 mL

Minimum Volume

0.5 mL (Note: This volume does not allow for repeat testing.)

Container

Red-top tube or gel-barrier tube

Stability Requirements

TemperaturePeriod
Room temperature14 days
Refrigerated14 days
Frozen14 days
Freeze/thaw cyclesStable x3

Storage Instructions

Maintain specimen at room temperature.

Causes for Rejection

Gross hemolysis; visible microbial contamination

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
006505 Cytomegalovirus IgG Avidity 52984-2 006506 CMV IgG Avidity Index Index 52984-2
Order Code006505
Order Code NameCytomegalovirus IgG Avidity
Order Loinc52984-2
Result Code006506
Result Code NameCMV IgG Avidity Index
UofMIndex
Result LOINC52984-2