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Test Code BART Bartonella Antibody Panel, IgG and IgM, Serum

Additional Codes

Epic Ordering Code LAB123008256
NBS code LBC02926
Service code 33162

Reporting Name

Bartonella Ab Panel, IgG and IgM

Specimen Type

Serum


Specimen Required


Supplies: Sarstedt Aliquot Tube 5 mL (T914)

Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 0.5 mL

Collection Instructions: Centrifuge and aliquot serum into plastic vial.


National University Hospital-Singapore Note:

NUH Outreach Laboratories:
Specimen Requirements
Submit only one of the following:
Preferred: Yellow Top
Acceptable: Red Top
Processing Requirements
Centrifuge and aliquot serum into a Mayo plastic tube.
Specimen type: Serum
Volume: 0.5 mL
Storage/transport requirements: Refrigerated

Forms

If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.

Specimen Minimum Volume

0.15 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 30 days
  Frozen  30 days

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject

Method Name

Immunofluorescence Assay (IFA)

Day(s) Performed

Monday through Saturday

Report Available

Same day/1 to 3 days
National University Hospital-Singapore Note:

Please note that this is a referral test requiring transport to the external testing facility and an additional 3-5 days is required.

Reference Values

BARTONELLA HENSELAE

IgG: <1:128

IgM: <1:20

 

BARTONELLA QUINTANA

IgG: <1:128

IgM: <1:20

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Useful For

Diagnosis of Bartonella infection, especially in the context of a cat scratch

CPT Code Information

86611 x 4

LOINC Code Information

Test ID Test Order Name Order LOINC Value
BART Bartonella Ab Panel, IgG and IgM 90251-0

 

Result ID Test Result Name Result LOINC Value
15659 Bart Henselae IgG In Process
15660 Bart Henselae IgM In Process
15661 Bart Quintana IgG In Process
15662 Bart Quintana IgM In Process

Test 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.
National University Hospital-Singapore Additional Information:

Updated on 29/09/2026