Cytomegalovirus (CMV), Quantitative, Urine, PCR
Also known as: CMV, PCR Quantitation
Use
This test is intended to be used to quantitatively detect CMV DNA in urine specimens as an aid to diagnosis and management of CMV infections.
Special Instructions
The test results have a quantitative range of 250−1,000,000 copies/mL. Specimens should be collected in a sterile urine container, without any preservatives. Ensure proper collection and handling of the urine specimen to prevent contamination and ensure accurate test results.
Limitations
The quantitative range of this assay is limited to 250−1,000,000 copies/mL. Results may be impacted by improper specimen handling, including contamination, insufficient volume, and improper storage conditions. The performance characteristics of this test have been developed by Labcorp and are not cleared or approved by the FDA.
Methodology
PCR-based (qPCR)
Biomarkers
LOINC Codes
- 49347-8
- 49347-8
- 53763-9
Result Turnaround Time
3-4 days
Related Documents
For more information, please review the documents below
Specimen
Urine
Volume
2 mL
Minimum Volume
0.5 mL
Container
Sterile urine container, no preservative
Storage Instructions
Refrigerate or freeze.
Causes for Rejection
Quantity not sufficient for analysis; gross specimen contamination; specimen too old; leaking or broken tube
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 7 days |
| Frozen | 7 days |
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