Test Code TFAM Rickettsia typhi (Typhus Fever) Antibody, IgM by IFA
Clinical Indications
Confirm presence of Rickettsia typhi. Panel test (IgG and IgM) is preferred. Requires comparison of acute- to convalescent-phase serology.
Additional Test Codes
Epic Order Name: TYPHUS FEVER ABS IGM (aka TFAM)
Sunquest Order Code: TFAM
Epic Px Code: LAB3003
Specimen Collection Type
Preferred: Gold
Acceptable: Red
Minimum Collection Volume
0.3 mL
Reference Range
Less than 1:64 |
Negative - No significant level of IgM antibody detected. |
1:64 or greater |
Positive - Presence of IgM antibody to detected, which may indicate a current or recent infection; however, low levels of IgM antibodies may occasionally persist for more than 12 months post-infection. |
Critical Value
N/A
Interpretation
Antibody reactivity to Rickettsia typhi antigen should be
considered group-reactive for the Typhus Fever group, which
includes Rickettsia prowazekii.
Seroconversion between acute and convalescent sera is considered
strong evidence of recent infection. The best evidence for
infection is a significant change (fourfold difference in titer) on
two appropriately timed specimens, where both tests are done in the
same laboratory at the same time. Acute-phase specimens are
collected during the first week of illness and convalescent-phase
samples are generally obtained 2-4 weeks after resolution of
illness. Ideally these samples should be tested simultaneously at
the same facility. If the sample submitted was collected during the
acute-phase of illness, submit a marked convalescent sample within
25 days for paired testing.
Rejection Criteria
Contaminated, hemolyzed, or severely lipemic, specimens.
Specimen Availability for Add-on Testing
2 Days
Specimen Stability
Refrigerated (preferred): 2 weeks
Ambient: 48 hours
Frozen: 1 year
Day(s) Performed
Sun-Sat
Performing Lab- Department
TUKHS-BH-Mail Outs
CPT Code
86757
LOINC Code
5325-6
Test Alias
R typhi IgM antibody
Typhus Fever Group IgM Antibody
Additional Information / Notes
N/A