Test ID CMVLR Cytomegalovirus (CMV) Molecular Detection, PCR, Lower Respiratory
Ordering Guidance
For plasma specimens, order CMVQN / Cytomegalovirus (CMV) DNA Detection and Quantification by Real-Time PCR, Plasma.
Necessary Information
Specimen source is required.
Specimen Required
Specimen Type: Lower respiratory
Source: Bronchial washing, bronchoalveolar lavage, fluid/washings from lung, sputum, tracheal secretions, tracheal aspirates
Container/Tube:
Preferred: Sterile, screwcap, 5-mL aliquot tube
Acceptable: Sterile container
Specimen Volume: 1 mL
Collection Instructions: Do not centrifuge.
Reporting Name
Cytomegalovirus, PCR, Lower RespSpecimen Type
VariesSpecimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Varies | Refrigerated (preferred) | 7 days |
| Frozen | 7 days |
Report Available
Same day/1 to 2 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| CMVLR | Cytomegalovirus, PCR, Lower Resp | 104760-4 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| CMVSS | Specimen Source | 31208-2 |
| 621771 | CMVLR, PCR | 104760-4 |
Useful For
Rapid qualitative detection of cytomegalovirus (CMV) DNA in lower respiratory specimens
This test is not intended for the monitoring of CMV disease progression or response to therapy.
Day(s) Performed
Monday through Sunday
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
87496
Specimen Minimum Volume
0.5 mL
Reference Values
Negative
Reference values apply to all ages.
Method Name
Real-Time Polymerase Chain Reaction (PCR)/DNA Probe Hybridization