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Test Code FCYTG Cytomegalovirus IgG Avidity


Specimen Required


Specimen Type: Serum

Container/Tube: Red

Specimen Volume: 1 mL

Collection Instructions: Draw blood in a plain, red-top tube, serum gel tube is acceptable. Spin down and send 1 mL of serum refrigerated in a plastic vial.


Method Name

Immunoassay

Reporting Name

Cytomegalovirus IgG Avidity

Specimen Type

Serum

Specimen Minimum Volume

0.5 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 14 days
  Frozen  30 days
  Ambient  7 days

Reject Due To

Hemolysis Mild OK; Gross reject

Clinical Information

Discrimination between recent (primary) and past cytomegalovirus (CMV) infection can be an important tool in the clinical management of pregnant women. Although nearly all individuals with recent CMV infection are positive for CMV IgM, individuals with past CMV may also express CMV IgM due to long-term IgM persistence or viral reactivation; thus, detection of CMV IgM is not a reliable indicator of recent CMV infection. Measurement of CMV IgG avidity can assist in discriminating recent from past CMV infection. A low avidity index is a reliable indicator of CMV infection within the previous 6 months, a high avidity index essentially excludes the possibility that infection occurred within the previous 4 months. Avidity index values should be considered within the context of other laboratory findings and clinical signs.

Reference Values

>0.70

Day(s) Performed

Sunday, Tuesday through Friday

Report Available

4 to 10 days

Performing Laboratory

Quest Diagnostics

Test Classification

This test was developed and its performance characteristics have been determined by Quest Diagnostics Infectious Disease. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

CPT Code Information

86644