Test ID QFEVR Q Fever Antibody Screen with Titer Reflex, Serum
Method Name
Enzyme-Linked Immunosorbent Assay (ELISA)
Ordering Guidance
Specimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 0.6 mL Serum
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Reporting Name
Q Fever Ab Scrn w/ Titer Reflex, SSpecimen Type
SerumSpecimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 7 days |
| Frozen | 7 days |
Report Available
1 to 4 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| QFEVR | Q Fever Ab Scrn w/ Titer Reflex, S | 23019-3 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| QFEVR | Q Fever Ab Scrn w/ Titer Reflex, S | 23019-3 |
Forms
If not ordering electronically, complete, print, and send an Infectious Disease Serology Test Request (T916) with the specimen.
Useful For
Screening for exposure to Coxiella burnetii, the causative agent of Q fever
This test should not be used as a screening procedure for the general population.
Reflex Tests
| Test ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|
| QFP | Q Fever IgM/IgG, Titer, S | No | No |
Testing Algorithm
If the Q fever serology result is reactive, then Q fever antibody confirmation by indirect immunofluorescence will be performed at an additional charge.
For more information see Infective Endocarditis: Diagnostic Testing for Identification of Microbiological Etiology.
Day(s) Performed
Sunday 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
86638
86638 x4 (if appropriate)
Special Instructions
Specimen Minimum Volume
Serum: 0.5 mL
Reference Values
Negative
Reference values apply to all ages