Test Code Billings Clinic:1926 Mayo:BABPB Babesia species, Molecular Detection, PCR, Blood
Ordering Guidance
This is a qualitative assay, and the results are reported either as negative or positive for targeted Babesia species DNA.
Specimen Required
Container/Tube: Lavender top (EDTA)
Specimen Volume: 1 mL
Collection Instructions: Send whole blood specimen in original tube. Do not aliquot.
Useful For
Initial screening or confirmatory testing for suspected babesiosis during the acute febrile stage of infection in patients from endemic areas, especially when Giemsa-stained peripheral blood smears do not reveal any organisms, or the organism morphology is inconclusive
Method Name
Real-Time Polymerase Chain Reaction (PCR)/DNA Probe Hybridization
Reporting Name
Babesia species PCR, BSpecimen Type
Whole Blood EDTASpecimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Whole Blood EDTA | Refrigerated | 7 days |
Reject Due To
Gross hemolysis | OK |
Gross lipemia | Reject |
Reference Values
Negative
Reference values apply to all ages.
Interpretation
A positive result indicates the presence of Babesia species DNA and is consistent with active or recent infection. While positive results are highly specific indicators of disease, they should be correlated with blood smear microscopy, serological results, and clinical findings.
A negative result indicates absence of detectable DNA from Babesia species in the specimen but does not always rule out ongoing babesiosis in a seropositive person since the parasitemia may be present at a very low level or may be sporadic.
Other tests to consider in the evaluation of a patient presenting with an acute febrile illness following tick exposure include serologic tests for Lyme disease (Borrelia burgdorferi) and molecular detection (polymerase chain reaction: PCR) for ehrlichiosis/anaplasmosis. For patients who are past the acute stage of infection, serologic tests for these organisms should be ordered prior to PCR testing.
Day(s) Performed
Report Available
Same day/1 to 4 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
87798 x2Â Â Â Â Â Â Â Â Â
87469Â Â
87999 (if appropriate for government payers)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
BABPB | Babesia species PCR, B | 88461-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
618317 | Babesia microti | 88452-8 |
618318 | Babesia duncani | 88451-0 |
618319 | Babesia divergens/MO-1 | 88450-2 |
Forms
If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.