Coccidioides Antibody Initial Screen, Reflex to CF & ID (Sendout)
General Information
- Lab Name
- Coccidiodies Ab Initial Screen, Reflex to CF & ID (Sendout)
- Lab Code
- RCOXIS
- Epic Ordering
- Coccidiodies Ab Initial Screen, Reflex to CF & ID (Sendout)
- External Test Id
- COXIS
- Description
Useful For:
- Detection of antibodies to Coccidioides immitis/posadasii
- This assay should not be used for monitoring response to therapy.
Testing Algorithm: If result is positive, then Coccidioides by complement fixation and immunodiffusion will be performed at additional charge.
Ordering Guidance: Preferred initial Coccidioides antibody screening test. Refer to Coccidioides Antibody, for follow-up, CF & ID (Sendout) [RSCOCC] for monitoring of known positives.
- References
- Mayo Clinical & Interpretive Information: Coccidioides Antibody Screen with Reflex, Serum
- Washington State Department of Health Notifiable Conditions: Coccidioidomycosis (Valley Fever)
- Synonyms
- Cocci serology, Coccidioides immitis, Coccidioides posadasii, COXIS, San Joaquin Valley Fever
- Components
-
Code Name RCOXSR Coccidioides Antibody Screen
Interpretation
- Method
Coccidioides Antibody Screen: Enzyme Immunoassay (EIA)
Reflex, if performed: Complement Fixation (CF) and Immunodiffusion (ID)
- Reference Range
- See individual components
- Ref. Range Notes
Reference Values: Negative
Interpretation:
Enzyme immunoassay (EIA) results greater than or equal to 0.75 will be reported as Reactive: Confirmatory testing by complement fixation and immunodiffusion has been ordered.
A reactive result is presumptive evidence that the patient was previously or is currently infected with Coccidioides immitis/posadasii.
EIA results less than 0.75 will be reported as Negative: Repeat testing on a new sample in 2 – 3 weeks if clinically indicated.
A negative result indicates the absence of antibodies to Coccidioides immitis/posadasii and is presumptive evidence that the patient has not been previously exposed to and is not infected with Coccidioides. However, a negative result does not preclude the diagnosis of coccidioidomycosis as the specimen may have been drawn before antibodies levels were detectable due to early acute infection or immunosuppression.
This test is designed for the qualitative detection of both IgM- and IgG-class antibodies against antigens from Coccidioides. The report will not indicate which class of antibody is present.
- Interferences and Limitations
Cautions:
All results from this assay must be correlated with clinical history, epidemiologic data, and other laboratory evidence.
Reactive results from this assay are not indicative of acute infection. Antibodies may be present from previous infection with Coccidioides immitis/posadasii.
Negative results may occur in patients with acute coccidioidomycosis in whom antibody levels have not yet become detectable.
Rarely, cross reactivity of the Coccidioides antibody screen may occur in patients infected with other dimorphic fungal agents including Histoplasma and Blastomyces. Therefore, all positive results must be confirmed by complement fixation and immunodiffusion.
- References
- Mayo Clinical & Interpretive Information: Coccidioides Antibody Screen with Reflex, Serum
- Washington State Department of Health Notifiable Conditions: Coccidioidomycosis (Valley Fever)
- Guidelines
Ordering & Collection
- Specimen Type
- Blood
- Collection
-
6 mL blood in GOLD SST or RED TOP tube
- Handling Instructions
Outside Laboratories: Centrifuge sample and transfer serum to a separate plastic vial. Refrigerate serum.
Stability: Refrigerated (preferred): 14 days; Frozen: 14 days; Ambient: Unacceptable.
Reject Due To: Gross hemolysis, gross lipemia.
- Quantity
-
requested: 2 mL serum
minimum: 1.7 mL serum
Processing
- Processing
Centrifuge sample and transfer serum to a separate plastic vial. Refrigerate serum.
Sendouts:
- Order Mayo Test: COXIS.
- Interfaced: Yes.
Stability: Refrigerated (preferred): 14 days; Frozen: 14 days; Ambient: Unacceptable.
Reject Due To: Gross hemolysis, gross lipemia.
Performance
- LIS Dept Code
- Sendouts Mayo Lab (RF) (MARF)
- Performing Location(s)
-
Sendout Mayo Clinic Laboratories (Superior Drive)
800-533-17103050 Superior Drive NW
Rochester, MN 55901 - Frequency
- Performed: Monday - Friday. Report Available: 1-7 days.
- Available STAT?
- No
Billing & Coding
- CPT codes
- 86635
- LOINC
- 40712-2
- Interfaced Order Code
- UOW4704