Test Details
Methodology
Enzyme immunoassay (EIA)
Result Turnaround Time
2 - 6 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.
Use
The clinical utility of serological testing for HHV-6 is largely limited to diagnosing infection in immunocompromised individuals and for indentifying past infection/exposure to roseola infantum. IgG seroconversion or detection of HHV-6 IgM antibody may indicate a recent primary infection, reactivation or reinfection. Please note that nucleic acid amplification (PCR) is the recommended testing method for diagnosis of active HHV-6 infection. This assay is a qualitative assay and as such the numeric result provided does not equate to an antibody titer.
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The clinical utility of serological testing for HHV-6 is largely limited to diagnosing infection in immunocompromised individuals and for indentifying past infection/exposure to roseola infantum. IgG seroconversion or detection of HHV-6 IgM antibody may indicate a recent primary infection, reactivation or reinfection. Please note that nucleic acid amplification (PCR) is the recommended testing method for diagnosis of active HHV-6 infection. This assay is a qualitative assay and as such the numeric result provided does not equate to an antibody titer. |
Special Instructions
Please note that nucleic acid amplification (PCR) is the recommended testing method for diagnosis of active HHV-6 infection.
Please note that nucleic acid amplification (PCR) is the recommended testing method for diagnosis of active HHV-6 infection. |
Limitations
This procedure may be considered by Medicare and other carriers as investigational and, therefore, may not be payable as a covered benefit for patients.
References
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
Collection Instructions
If tube other than a gel-barrier tube is used, transfer separated serum to a plastic transport tube. Do not freeze gel-barrier tube (pour off serum first).
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If tube other than a gel-barrier tube is used, transfer separated serum to a plastic transport tube. Do not freeze gel-barrier tube (pour off serum first). |
Stability Requirements
Temperature | Period |
---|---|
Room temperature | 14 days |
Refrigerated | 14 days |
Frozen | 14 days |
Freeze/thaw cycles | Stable x4 |
Reference Range
• Negative: <0.90 index
• Equivocal: 0.90−1.10 index
• Positive: >1.10 index
• Negative: <0.90 index • Equivocal: 0.90−1.10 index • Positive: >1.10 index
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• Negative: <0.90 index • Equivocal: 0.90−1.10 index • Positive: >1.10 index
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Storage Instructions
Room temperature
Causes for Rejection
Hemolysis; lipemia; gross bacterial contamination
LOINC® Map
Order Code | Order Code Name | Order Loinc | Result Code | Result Code Name | UofM | Result LOINC |
---|---|---|---|---|---|---|
161075 | HHV 6 IgG Antibodies | 41148-8 | 161076 | HHV 6 IgG Antibodies | index | 41148-8 |
Order Code | 161075 | |||||
Order Code Name | HHV 6 IgG Antibodies | |||||
Order Loinc | 41148-8 | |||||
Result Code | 161076 | |||||
Result Code Name | HHV 6 IgG Antibodies | |||||
UofM | index | |||||
Result LOINC | 41148-8 |