Cytomegalovirus (CMV), Amniotic Fluid, PCR
Also known as: CMV, Amniotic Fluid
Use
This test is intended to be used as an aid in the diagnosis of CMV infection.
Special Instructions
Not provided.
Limitations
This test was developed and its performance characteristics determined by LabCorp. It has not been cleared or approved by the Food and Drug Administration (FDA), as the FDA has determined that such clearance or approval is not necessary. Possible limitations include false negatives if the viral load is below the detection limit or if improper specimen handling occurs.
Methodology
PCR-based (RT-PCR)
Biomarkers
LOINC Codes
- 34719-5 - CMV DNA Amn Ql NAA+probe
Result Turnaround Time
4-6 days
Related Documents
For more information, please review the documents below
Specimen
Amniotic Fluid
Volume
1 mL
Minimum Volume
0.2 mL
Container
Sterile container
Collection Instructions
Submit specimens in sterile containers. Ensure no contamination and avoid delays by submitting separate frozen specimens.
Storage Instructions
Freeze (preferred) or refrigerate.
Causes for Rejection
Quantity not sufficient for analysis; gross contamination; specimen too old; leaking or broken tube
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 3 days |
| Refrigerated | 7 days |
| Frozen | 90 days |
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