Coccidioides Antibody Screen, Reflex to CF & ID (Sendout)

General Information

Lab Name

Coccidioides Antibody Screen, Reflex to CF & ID (Sendout)

Lab Code

RCOXIG

Epic Name

Coccidioides Antibody 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

    Synonyms

    Cocci serology, Coccidioides immitis, Coccidioides posadasii, COXIS, San Joaquin Valley Fever

    Components

    Code Name
    RCOXIS Coccidioides Antibody Initial Screen with Reflex
    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 Value: 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.

      Guidelines

      Ordering & Collection

      Specimen Type

      Blood

      Collection

      7-10 mL blood in GOLD SST or RED TOP tube

      Handling Instructions

      Outside Laboratories: Centrifuge sample and aliquot serum to a separate plastic vial. Refrigerate serum while awaiting shipment. Transport with a cold pack.

      Stability: Refrigerated (preferred): 14 days; Frozen: 14 days; Ambient: Unacceptable.

      Reject Due To: Gross hemolysis, gross lipemia.

      Quantity

      requested: 2 mL serum + 2 mL serum for UW449
      minimum: 1.7 mL serum

      Processing

      Centrifuge sample and aliquot serum to two separate plastic vials. If sample volume is low, prioritize the sendout test (RCOXIS).

      • RCOXIS: Refrigerate serum in Sendouts Mayo Rack (95).
      • UW449: Forward sample to UW-MT Microbiology Lab.

      Sendouts:

      • Order Mayo Test: COXIS
      • Interfaced: Yes [Interface: 601; Worksheet: MARF]

      Stability: Refrigerated (preferred): 14 days; Frozen: 14 days; Ambient: Unacceptable.

      Reject Due To: Gross hemolysis, gross lipemia.

      Performance

      LIS Dept Code

      Performing Location(s)

      Sendout Mayo Clinic Laboratories (Superior Drive)
      800-533-1710

      3050 Superior Drive NW
      Rochester, MN 55901

      Frequency

      Performed: Monday through Friday. Reported: 1-7 days from sample receipt at Mayo Clinic Labs.

      Available STAT?

      No

      Billing & Coding

      CPT codes

      86635

      LOINC

      40712-2

      Interfaced Order Code

      UOW6134