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 AviditySpecimen Type
SerumSpecimen 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 daysPerforming Laboratory
Quest DiagnosticsTest 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