Coxiella Burnetii IgG Abs




Test Mnemonic

COXIGG

CPT Codes

  • 86638 - QTY (2)

Aliases

  • Coxiella Burnetii IgG Phase 1&2
  • Q-Fever IgG
  • C. burnetii Ab IgG, Phase I and II with Reflex to Titer

Includes

  • IgG Phase 1
  • IgG Phase 2

Performing Laboratory

ARUP


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
1 mLSerumSST (Gold) RefrigeratedSeparate serum from cells ASAP or within 2 hours of collection and transfer into standard aliquot tube. Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Label specimens plainly as 'acute' and 'convalescent.'

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
0.4 mL     

Stability

Environmental Condition Description
RefrigeratedAfter separation from cells: 2 weeks
FrozenAfter separation from cells: 1 year (Avoid repeated freeze/thaw cycles)
AmbientAfter separation from cells: 48 hours

Days Performed

Mon, Wed, Fri

Turnaround Time

2 - 7 days

Methodology

Name Description
Semi-Quantitative Indirect Fluorescent Antibody 

Reference Range

Special Info

Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. If either C. Burnetii Abs IgG Phase I and/or Phase II result is indeterminate or positive, then titer(s) will be added at an additional cost. Contaminated, hemolyzed, or severely lipemic specimens are unacceptable. This test is New York DOH approved.

Clinical Info

Useful to confirm infectious agent as C. burnetii (Q-fever) in symptomatic patients. Testing of acute and convalescent sera is recommended. Single phase II IgG titers of 1:256 and greater are considered evidence of C. burnetii infection at some time prior to the date of the serum specimen. Phase I antibody titers of 1:16 and greater are consistent with chronic infection or convalescent phase of Q-fever.