Test Code CCMVU Congenital Cytomegalovirus (cCMV), Molecular Detection, PCR, Urine
Ordering Guidance
This test should be ordered to test urine specimens from patients aged 21 days or younger. To test urine from patients older than 21 days, order CMVPV / Cytomegalovirus (CMV) Molecular Detection, PCR, Varies.
To test saliva specimens from patients aged 21 days or younger, order CCMVS / Congenital Cytomegalovirus (cCMV), Molecular Detection, PCR, Saliva. To test saliva from patients older than 21 days, order CMVPV / Cytomegalovirus (CMV) Molecular Detection, PCR, Varies.
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Container/Tube: Plastic sterile container, 5 mL
Specimen Volume: 0.2 mL
Collection Instruction:
1. Collect a random urine from a urine bag, container, or catheter.
2. Transfer urine to sterile container.
3. No preservative
Secondary ID
620658Useful For
Aiding in the rapid diagnosis of cytomegalovirus infections in neonates 21 days of age or younger using urine specimens
Method Name
Real-Time Polymerase Chain Reaction (PCR)
Specimen Type
UrineSpecimen Minimum Volume
0.1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Urine | Frozen | 72 hours |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
Negative
Interpretation
A positive result indicates the presence of cytomegalovirus (CMV) DNA in the patient sample.
A negative result indicates the absence of CMV DNA in the patient sample.
An invalid result indicates inability to conclusively determine presence or absence of CMV DNA in the patient sample.
Method Description
The Simplexa Congenital CMV (cytomegalovirus) Direct assay is a real-time polymerase chain reaction system that enables the direct amplification and detection of CMV DNA from either saliva swab or urine specimens without nucleic acid extraction. The system consists of the Simplexa Congenital CMV Direct Reaction Mix, the LIAISON MDX (with LIAISON MDX Studio Software), the direct amplification disc, and associated accessories.
In the Simplexa Congenital CMV Direct assay, bifunctional fluorescent probe-primers are used together with corresponding reverse primers to amplify CMV DNA. A well-conserved region of the CMV UL83 gene is targeted to identify CMV DNA. An internal control is used to detect PCR failure and/or inhibition.(Package insert: Simplexa Congenital CMV Direct. Diasorin; REF MOL2255. Rev. 01, 11/2022)
Day(s) Performed
Monday through Sunday
Report Available
Same day/1 to 2 daysSpecimen Retention Time
3 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterCPT Code Information
87496
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
CCMVU | Congenital CMV, PCR, Urine | 4999-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
620658 | Congenital CMV, PCR, Urine | 4999-9 |