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Test ID: FFAPL
Febrile Antibodies Panel

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

Yes

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
FRMFGRMSF IgG TiterNoNo
FRMFMRMSF IgM TiterNoNo
FRTGR. Typhi IgG TiterNoNo
FRTMR. Typhi IgM TiterNoNo
FBRAGBrucella AgglutinationNoNo

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

If RMSF IgG is Detected, then FRMFG RMSF IgG Titer will be performed at an additional charge.

If RMSF IgM is Detected, then FRMFM RMSF IgM Titer will be performed at an additional charge.

If R. Typhi IgG is Detected, then FRTG R. Typhi IgG Titer will be performed at an additional charge.

If R. Typhi IgM is Detected, then FRTM R. Typhi IgM Titer will be performed at an additional charge.

If Brucella IgM is > or =1.10, then FBRAG Brucella Agglutination will be performed at an additional charge.

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

Immunofluorescence Assay (IFA)

Enzyme Immunoassay (EIA)

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

Febrile Antibodies Panel

Specimen Type Describes the specimen type needed for testing

Serum

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.

Draw blood in a plain, red-top tube(s) or serum gel tube(s). Spin down and send 3 mL of serum refrigerated.

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.

0.8 mL

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

Hemolysis

NA

Thawing

Warm OK; Cold 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
SerumRefrigerated (preferred)14 days
 Frozen 30 days
 Ambient 7 days

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.

Rickettsia (Typhus Fever) Antibodies (IgG, IgM) with Reflex to Titers

 Reference Range: Not Detected

 

Rickettsia (RMSF) Antibodies (IgG, IgM) with Reflex to Titers

 Reference Range: Not Detected

 

Salmonella Antibodies, EIA

 Reference Range: Not Detected

 

Antibodies to Salmonella flagellar (H) and somatic (O) antigens typically peak 3 – 5 weeks after infection. A positive results in this assay is equivalent to a titer of >=1:160 by tube agglutination (Widal). Results should not be considered as diagnostic unless confirmed by culture.

 

Brucella Antibodies (IgG, IgM), EIA with Reflex to Agglutination

 Reference Range: <0.80

 

 Interpretive Criteria:

            <0.80 Antibody not detected

            0.80 – 1.09 Equivocal

            > or = 1.10 Antibody detected

 

Acute brucellosis is characterized by the appearanceof Brucella-specific IgM within the first week of infection, followed by the appearance of Brucella-specific IgG after the second week. Levels of both IgM and IgG decline slowly over several months in conjunction with recovery. Persistence of high IgG levels with declining or absent IgM suggests chronic infection or relapse.

 

Test Performed by:         Focus Diagnostics, Inc.

                                    5785 Corporate Avenue

                                    Cypress, CA 90630-4750

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.

Varies; Monday through Friday

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.

1 - 4 days

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

3 - 8 days

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

Focus Diagnositics, Inc.

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.

86622/x2 Brucella

86757/x4 Rickettsia

86768/x5 Salmonella

86757/ each Rickettsia titer, if appropriate

86622/Brucella 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
Z2793RMSF IgGIn Process
Z2794RMSF IgMIn Process
Z2795R. Typhi IgGIn Process
Z2796R. Typhi IgMIn Process
Z2788Salmonella H, Type aIn Process
Z2789Salmonella H, Type bIn Process
Z2790Salmonella H, Type dIn Process
Z2791Salmonella O, Type ViIn Process
Z2792Salmonella O, Type DIn Process
Z2797Brucella IgGIn Process
Z2798Brucella IgMIn Process