CMV, IgG




Test Mnemonic

CMVG

CPT Codes

  • 86644 - QTY (1)

Aliases

  • Cytomegalovirus Antibody IgG

Performing Laboratory

Cleveland Clinic Laboratories

FDA Category

In Vitro Diagnostic


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
1 mLSerumSST (Gold) Refrigerated 

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
0.5 mL     

Stability

Environmental Condition Description
Ambient24 hours
Refrigerated7 days
Frozen14 days

Days Performed

Mon, Wed, Fri

Turnaround Time

1 - 4 days

Methodology

Name Description
Chemiluminescence Immunoassay (CLIA) 

Reference Range

CMV IgG Qual
Sex Age From Age To Type Range Range Unit
       NormalNegative 
Cytomegalovirus IgG
Sex Age From Age To Type Range Range Unit
       NormalRefer to report 

Special Info

Grossly hemolyzed, icteric or lipemic samples as well as samples containing particulate matter or exhibiting obvious microbial contamination will be rejected.

Clinical Info

The presence of CMV IgM should also be determined to assess the stage of CMV infection. Diagnosis of infectious diseases should not be established on the basis of a single test result, but should be determined in conjunction with clinical findings and other diagnostic procedures as well as in association with medical judgment. Diseases such as Epstein-Barr viral syndrome, toxoplasmosis and hepatitis may cause symptoms similar to CMV infection and must be excluded before confirmation of diagnosis.

Clinical Limitation

Results from immunosuppressed patients should be interpreted with caution. Screening of the general population should not be performed. The positive predictive value depends on the likelihood of the virus being present. Testing should only be performed on patients with clinical symptoms or when exposure is suspected.