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Test ID: FSC
Fungal Antibody Survey, Spinal Fluid

Secondary ID A test code used for billing and in test definitions created prior to November 2011

83120

NY State Approved Indicates the status of NY State approval and if the test is orderable for NY State clients.

No

Useful For Suggests clinical disorders or settings where the test may be helpful

Rapid screening for fungal meningitis when evidence for a specific organism is lacking

Profile Information A profile is a group of laboratory tests that are ordered and performed together under a single Mayo Test ID. Profile information lists the test performed, inclusive of the test fee, when a profile is ordered and includes reporting names and individual availability.

Test IDReporting NameAvailable SeparatelyAlways Performed
CCOCCocci CF and ID, CSFYesYes
CCRYPCryptococcus Ag Screen, CSFYesYes
CHISTHistoplasma Ab, CSFYesYes
CBLASBlastomyces Ab, EIA, CSFYesYes

Reflex Tests Lists test(s) that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial test(s)

Test IDReporting NameAvailable SeparatelyAlways Performed
CCRYRCryptococcus Ag, CSFYesNo

Testing Algorithm Delineates situation(s) when tests are added to the initial order. This includes reflex and additional tests.

If Cryptococcus antigen screen result is reactive (by EIA), then latex agglutination testing (CCRYR/28072 Cryptococcus Antigen, Spinal Fluid) will be performed at an additional charge.

Method Name A short description of the method used to perform the test

CCOC/81542: Complement Fixation (CF) Using Coccidioidin: IgG/Immunodiffusion: IgG and IgM

CCRYP/86166, CBLAS/89986: Enzyme Immunoassay (EIA)

CHIST/8230: Complement Fixation (CF)/Immunodiffusion

CCRYR/28072: Latex Agglutination

Reporting Name A shorter/abbreviated version of the Published Name for a test; an abbreviated test name

Fungal Ab Survey, CSF

Aliases Lists additional common names for a test, as an aid in searching

Fungus serology

Specimen Type Describes the specimen type needed for testing

CSF

Specimen Required Defines the optimal specimen. This field describes the type of specimen required to perform the test and the preferred volume to complete testing. The volume allows automated processing, fastest throughput and, when indicated, repeat or reflex testing.

Container/Tube: Sterile vial

Specimen Volume: 3 mL

Specimen Minimum Volume Defines the amount of specimen required to perform an assay once, including instrument and container dead space. Submitting the minimum specimen volume makes it impossible to repeat the test or perform confirmatory or perform reflex testing. In some situations, a minimum specimen volume may result in a QNS (quantity not sufficient) result, requiring a second specimen to be collected.

2.6 mL

Reject Due To Identifies specimen types and conditions that may cause the specimen to be rejected

Hemolysis

Mild OK; Gross OK

Lipemia

NA

Icterus

NA

Other

NA

Specimen Stability Information Provides a description of the temperatures required to transport a specimen to the laboratory. Alternate acceptable temperature(s) are also included.

Specimen TypeTemperatureTime
CSFRefrigerated (preferred)14 days
 Frozen 14 days

Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

See individual test IDs

Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

Blastomyces ANTIBODY BY EIA

Negative

 

Coccidioides ANTIBODY

Complement fixation: negative

If positive, results are titered.

Immunodiffusion: negative

Results are reported as positive, negative, or equivocal.

 

Cryptococcus ANTIGEN SCREEN

Negative

If reactive, results are titered under the reflex test.

 

Histoplasma ANTIBODY

Mycelial by complement fixation: negative

Positives are reported as titer.

Yeast by complement fixation: negative

Positives are reported as titer.

Antibody by immunodiffusion: negative

Positives are reported as band present.

Interpretation Provides information to assist in interpretation of the test results

See individual test IDs

Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

Cross-reacting antibodies may be produced and sometimes present interpretive problems.

Clinical Reference Provides recommendations for further in-depth reading of a clinical nature

Kaufman L, Kovacs JA, Reiss E: Clinical immunomycology. In Manual of Clinical Laboratory Immunology. Fourth edition. Edited by EC DeMarcario, Washington, DC. ASM Press, 1997

Method Description Describes how the test is performed and provides a method-specific reference

See individual test IDs

Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.

Blastomyces antibody: Monday through Friday; Sunday; 11 a.m.

Coccidioides: Monday through Friday; 11 a.m.

Cryptococcus antigen: Monday through Friday; 11 a.m. and 8 p.m., Sat, Sun; 11a.m.

Histoplasma antibody: Monday through Friday; 11 a.m.

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

3 days

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

6 days

Specimen Retention Time Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

14 days

Performing Laboratory Location The location of the laboratory that performs the test

Rochester

CPT Code Information Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Medical Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

86612-Blastomyces

86635 x 3-Coccidioides

86698 x 3-Histoplasma

87327-Cryptococcus EIA

86403-Cryptococcus latex agglutination (if appropriate)

LOINC® Code Information Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the result codes returned for this test or profile.

Result IDReporting NameLOINC Code
CBLASBlastomyces Ab, EIA, CSF18197-4
86166Cryptococcus Ag Screen, CSF29896-8
81542Cocci Ab, CF (CSF)30209-1
15118Histoplasma Mycelial (CSF)12456-0
15119Histoplasma Yeast (CSF)12455-2
21002Cocci ID-IgG (CSF)In Process
21001Cocci ID-IgM (CSF)In Process
15120Histoplasma Immunodiffusion (CSF)21330-6