Babesia microti Antibodies (IgG, IgM) with Reflex to Titers

Babesia microti Antibodies (IgG, IgM) with Reflex to Titers

Test Code

16194
86753 (x2)
16194
86753 (x2)
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

Babesia microti Antibodies (IgG, IgM) with Reflex to Titers - This test is for the detection of IgG and IgM antibodies against Babesia microti to aid in the diagnosis of Babesiosis. Babesiosis is a tickborne disease caused by transmission of the protozoa via the bite of an infected tick. B. microti is most common in the northern and upper Midwestern United States.

Testing for B. microti is based on a clinical evaluation and risk of tick exposure with consideration to the geographic region. Symptoms may be nonspecific, including headache, fever/chills, malaise, myalgia, and gastrointestinal symptoms. Infection can have similarities with ...

Test Details

Includes

  • If Babesia microti (IgG) is Detected, then Babesia microti (IgG) Titer will be performed at an additional charge (CPT code(s): 86317).
    If Babesia microti (IgM) is Detected, then Babesia microti (IgM) Titer will be performed at an additional charge (CPT code(s): 86317).

Methodology

Immunofluorescence Assay (IFA)

Assay Category

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

Babesia microti Ab (IgG), ScreenNot Detected
Babesia microti Ab (IgM), ScreenNot Detected
   
   Babesia microti Ab (IgG), Titer<1:64 titer
   Babesia microti Ab (IgM), Titer<1:20 titer

Alternative Name(s)

Babesiosis IgG & IgM,Human Babesiosis

LOINC® Codes, Performing Laboratory

If Babesia microti (IgG) is Detected, then Babesia microti (IgG) Titer will be performed at an additional charge (CPT code(s): 86317).
If Babesia microti (IgM) is Detected, then Babesia microti (IgM) Titer will be performed at an additional charge (CPT code(s): 86317).

Methodology

Immunofluorescence Assay (IFA)
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Reference Range(s)

Babesia microti Ab (IgG), ScreenNot Detected
Babesia microti Ab (IgM), ScreenNot Detected
   
   Babesia microti Ab (IgG), Titer<1:64 titer
   Babesia microti Ab (IgM), Titer<1:20 titer

Alternative Name(s)

Babesiosis IgG & IgM,Human Babesiosis

Preferred Specimen(s)

1 mL serum

Minimum Volume

0.2 mL

Transport Container

Transport tube

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Room temperature: 72 hours
    Refrigerated: 7 days
    Frozen: 30 days

Setup Schedule

1 mL serum
0.2 mL
Transport tube
Refrigerated (cold packs)
Room temperature: 72 hours
Refrigerated: 7 days
Frozen: 30 days
In-home collection may be available in your area for purchase through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

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