Bartonella henselae (Cat Scratch) Antibodies, IgG & IgM by IFA
0050108
Ordering Recommendation
May assist in diagnosing cat scratch disease in patient with typical signs and symptoms and a compatible exposure history.
Mnemonic
CATSCRATCH
Methodology
Semi-Quantitative Indirect Fluorescent Antibody
Performed
Mon, Thu
Reported
1-8 days  
New York DOH Approval Status
This test is New York DOH approved.
Submit With Order
 
Specimen Required
Patient Preparation
  
Collect
Serum separator tube.  
Specimen Preparation
Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.15 mL) Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Mark specimens plainly as acute or convalescent.  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Contaminated, hemolyzed, or severely lipemic specimens.  
Remarks
  
Stability
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)  
Reference Interval
 
 
Test Number Components Reference Interval
0050091Bartonella henselae Antibody, IgG by IFA <1:64  Negative -​ No significant level of Bartonella henselae IgG antibody detected.
1:64-​1:128  Equivocal -​ Questionable presence of Bartonella henselae IgG antibody detected.  Repeat testing in 10-​14 days may be helpful.
≥1:256  Positive -​ Presence of IgG antibody to Bartonella henselae detected, suggestive of current or past infection.
0050092Bartonella henselae Antibody, IgM by IFA < 1:16  Negative -​ No significant level of Bartonella henselae IgM antibody detected.
≥ 1:16  Positive -​ Presence of IgM antibody to Bartonella henselae detected, suggestive of current or recent infection.
Interpretive Data
Refer to individual components.

See Compliance Statement A: www.aruplab.com/CS
Statement A: Analyte specific reagents (ASR) are used in many laboratory tests necessary for standard medical care and generally do not require U.S. Food and Drug Administration (FDA) approval or clearance. This test was developed and its performance characteristics determined by ARUP Laboratories. The U.S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions. This test should not be regarded as investigational or for research use.
 
Note
 
CPT Code(s)
86611 x2
Components
Component Test Code*Component Chart NameLOINC
0050091Bartonella henselae Antibody IgG6954-2
0050092Bartonella henselae Antibody IgM6955-9
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Aliases
  • B henselae IgG
  • B henselae IgM
  • Bartonella henselae Abs
  • Cat Scratch Disease Ab Panel, Serum