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HelpTest ID CBSRP Coxiella burnetii (Q Fever), Molecular Detection, PCR, Serum
Useful For
Aiding in the diagnosis of Coxiella burnetii infection (ie, Q fever) using serum specimens
Method Name
Real-Time Polymerase Chain Reaction (PCR)
Reporting Name
Coxiella burnetii (Q fever) PCR, SSpecimen Type
SerumSpecimen 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.
Collection Container/Tube:
Preferred: Red top
Acceptable: Serum gel
Submission Container/Tube: Sterile vial
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot serum into a sterile vial within 2 hours of collection.
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Serum | Frozen (preferred) | 7 days | |
| Refrigerated | 7 days |
Reference Values
Not applicable
Day(s) Performed
Monday through Friday
Performing Laboratory
Mayo Clinic Laboratories in Rochester
CPT Code Information
87798
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| CBSRP | Coxiella burnetii (Q fever) PCR, S | 90443-3 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 35189 | Specimen Source | 31208-2 |
| 35190 | Coxiella burnetii PCR | 90443-3 |
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.Report Available
2 to 7 daysNY State Approved
YesForms
If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.