Francisella tularensis Antibody, Direct Agglutination (DA) [35176X]

Test Code
116982

CPT Codes
86000

Preferred Specimen
1 mL serum

Minimum Volume
0.5 mL

Transport Container
Plastic screw-cap vial

Transport Temperature
Room temperature

Specimen Stability
Room temperature: 7 days
Refrigerated: 14 days
Frozen: 30 days

Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Grossly hemolyzed • Hyperlipemic • Contaminated • Icteric • Turbid sera • CSF and other fluids are not acceptable

Methodology

Direct Agglutination (DA)



FDA Status
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.

Setup Schedule
Set up: Tues-Sat; Report available: 2-4 days

Limitations
Test may demonstrate crossreactivity with brucella, Proteus OX-19, and Yersinia species. Antibodies may be elevated many years after infection.

Reference Range
See Laboratory Report

Clinical Significance
Tularemia antibody titers ≥ 1:20 are of diagnostic significance. However, titers in this range may also indicate previous infection. Antibody begins to appear 2-3 weeks post-onset and generally peaks at approximately 5 weeks into the disease. Based on this antibody production pattern, a second specimen will usually demonstrate a diagnostic fourfold rise in titer for patients with active disease.

Performing Laboratory
Quest Diagnostics Infectious Disease, Inc.
33608 Ortega Highway, Bldg B-West Wing
San Juan Capistrano, CA 92675-2042




The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.