ARUP's Laboratory Test Directory

Leishmania Antibody, IgG (Visceral Leishmaniasis) : 0051726

Mnemonic: LEISH IGG

Methodology: Semi-Quantitative Immunoassay
Performed: Tue
Reported: 1-8 days
Specimen Required: Collect: Serum separator tube.

Specimen Preparation: Transfer 0.5 mL serum to an ARUP Standard Transport Tube. (Min: 0.1 mL)

Storage/Transport Temperature: Refrigerated.

Unacceptable Conditions: Serum or plasma containing glycerol or other viscous materials. Hemolyzed specimens.

Stability (collection to initiation of testing): After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year

Reference Interval:
0 Units: Negative - No Significant level of Leishmania Antibody, IgG detected.
1-15 Units: Positive - IgG antibody to Leishmania detected, which may suggest current or past infection.
Interpretive Data: Detection of IgG antibody directed at Leishmania may suggest current or past infection.
CPT Code(s): 86717
Cross References: Kala azar (Leishmania Antibody, IgG (Visceral Leishmaniasis)) , Kalazar Detect Test (Leishmania Antibody, IgG (Visceral Leishmaniasis)) , Leishmania donovani Antibodies (Leishmania Antibody, IgG (Visceral Leishmaniasis))
 
 

 

 

 
All ARUP Sites:        www.aruplab.com     ·     www.arupconsult.com     ·     www.arup.utah.edu     ·     www.childx.org     ·     www.utahblood.org