Test Code QFEVR Q Fever Antibody Screen with Titer Reflex, Serum
Additional Codes
| Epic Ordering Code | LAB3040844 |
| NBS code | |
| Service code | 33159 |
Reporting Name
Q Fever Ab Scrn w/ Titer Reflex, SSpecimen Type
SerumOrdering 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.
NUH Outreach Laboratories:
Specimen Requirements
Submit only one of the following:
Preferred: Yellow Top
Acceptable: Red Top
Processing Requirements
Centrifuge and aliquot serum into a Mayo plastic tube.
Specimen type: Serum
Volume: 0.6 mL
Storage/transport requirements: Refrigerated
Forms
If not ordering electronically, complete, print, and send an Infectious Disease Serology Test Request (T916) with the specimen.
Special Instructions
Specimen Minimum Volume
Serum: 0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 7 days |
| Frozen | 7 days |
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | Reject |
| Gross icterus | Reject |
| Heat-inactivated specimen | Reject |
Method Name
Enzyme-Linked Immunosorbent Assay (ELISA)
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.
Reflex Tests
| Test ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|
| QFP | Q Fever IgM/IgG, Titer, S | No | No |
Day(s) Performed
Sunday through Friday
Report Available
1 to 4 daysPlease note that this is a referral test requiring transport to the external testing facility and an additional 3-5 days is required.
Reference Values
Negative
Reference values apply to all ages
Performing Laboratory
Mayo Clinic Laboratories in Rochester
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.
CPT Code Information
86638
86638 x4 (if appropriate)
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 |
Secondary ID
616832Test 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.Last updated 05/08/2026