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Spotted Fever Group Antibodies, IgG and IgM

CPT 86757(x2)
Synonyms
  • Rickettsia rickettsii Antibodies
  • Rickettsia rickettsii IgG and IgM
  • Rocky Mountain Spotted Fever (RMSF) Antibodies
  • Rocky Mountain Spotted Fever (RMSF) IgG and IgM

Test Details

Methodology

Semi-quantitative indirect fluorescent antibody (IFA)

Result Turnaround Time

4 - 5 days

Turnaround time is defined as the usual number of days from the date of pickup of a specimen for testing to when the result is released to the ordering provider. In some cases, additional time should be allowed for additional confirmatory or additional reflex tests. Testing schedules may vary.

Related Documents

Use

The test is useful in the diagnosis of spotted fever group rickettsial infections.

Antibody reactivity to Rickettsia rickettsii antigen should be considered Spotted Fever group reactive. Other organisms within the group include R. akari, R. conorrii, R. australis and R. sibirica. This test is preferred for the acute or convalescent phase of disease. Acute and convalescent titers are often necessary. IgG serum endpoint titer of ≥1:64 is suggestive of infection at an unknown time and may be a sign of either past infection or early response to a recent infection. IgM titer of ≥1:64 is regarded as probable evidence of recent or ongoing infection. A four-fold or greater increase in titer between two serum samples drawn 1-2 weeks apart and tested in parallel is the best serologic indicator of a recent rickettsial infection.

Limitations

This test is preferred for the acute or convalescent phase of disease. Acute and convalescent titers are often necessary. The CDC does not use IgM results for routine diagnostic testing of Rocky Mountain Spotted Fever, as the response may not be specific for the agent (resulting in false positives) and the IgM response may be persistent from past infection.

This test was developed and its performance characteristics determined by Labcorp. It has not been cleared or approved by the Food and Drug Administration.

Specimen Requirements

Specimen

Serum

Volume

0.4 mL

Minimum Volume

0.2 mL (Note: This volume does not allow for repeat testing.)

Container

Gel-barrier tube, red-top tube or serum transfer tube

Storage Instructions

Room temperature

Causes for Rejection

Hemolysis; lipemia; gross bacterial contamination

LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
016502 Spotted Fever Group Antibodies 90260-1 016503 Spotted Fever Group IgG 22477-4
016502 Spotted Fever Group Antibodies 90260-1 016504 Spotted Fever Group IgM 22479-0
016502 Spotted Fever Group Antibodies 90260-1 016505 Result Comment: N/A
Order Code016502
Order Code NameSpotted Fever Group Antibodies
Order Loinc90260-1
Result Code016503
Result Code NameSpotted Fever Group IgG
UofM
Result LOINC22477-4
Order Code016502
Order Code NameSpotted Fever Group Antibodies
Order Loinc90260-1
Result Code016504
Result Code NameSpotted Fever Group IgM
UofM
Result LOINC22479-0
Order Code016502
Order Code NameSpotted Fever Group Antibodies
Order Loinc90260-1
Result Code016505
Result Code NameResult Comment:
UofM
Result LOINCN/A