Test Code CBBRPSO Coxiella burnetii (Q Fever), Molecular Detection, PCR, Blood
Additional Codes
Mayo Test Code: CBBRP
Reporting Name
Coxiella burnetii (Q fever) PCR, BUseful For
Aiding in the diagnosis of Coxiella burnetii infection (eg, Q fever)
Performing Laboratory
Mayo Clinic Laboratories in Rochester
Specimen Type
Whole Blood EDTAOrdering Guidance
Specimen Required
The high sensitivity of amplification by polymerase chain reaction requires the specimen to be processed in an environment in which contamination of the specimen by Coxiella burnetii DNA is unlikely.
Container/Tube:
Preferred: Lavender top (EDTA)
Acceptable: Royal blue top (EDTA), pink top (EDTA), or sterile vial containing EDTA-derived aliquot
Specimen Volume: 1 mL
Collection Instructions: Send whole blood specimen in original tube (preferred).
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Whole Blood EDTA | Refrigerated (preferred) | 7 days |
| Frozen | 7 days |
Reference Values
Not applicable
Day(s) Performed
Monday through Friday
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
87798
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| CBBRP | Coxiella burnetii (Q fever) PCR, B | 90443-3 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 35191 | Specimen Source | 31208-2 |
| 35192 | Coxiella burnetii PCR | 90443-3 |
Cautions
Test results should be used as an aid in diagnosis and not be considered diagnostic in themselves. A single assay should not be used as the only criteria to form a clinical conclusion, but results should be correlated with patient symptoms and clinical presentation. A negative result does not negate the presence of the organism or active disease.
Report Available
Same day/1 to 4 daysSpecimen Retention Time
1 weekReject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Method Name
Real-Time Polymerase Chain Reaction (PCR)
Forms
If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.
Testing Algorithm
For information see Infective Endocarditis: Diagnostic Testing for Identification of Microbiological Etiology.