Histoplasma Antigen by EIA, Serum
0092522
Ordering Recommendation
 
Mnemonic
HISTOAG S
Methodology
Semi-quantitative Enzyme Immunoassay
Performed
Sun-Sat
Reported
1-2 days  
New York DOH Approval Status
Specimens from New York clients will be sent out to a New York DOH approved laboratory, if possible.
Submit With Order
Specimen Required
Patient Preparation
  
Collect
Serum separator tube.  
Specimen Preparation
Transfer 2 mL serum to an ARUP Standard Transport Tube (ARUP Supply #43115). (Min: 1 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Urine (refer to test Histoplasma Galactomannan Antigen Quantitative by EIA, Urine (ARUP test code 2009418). Specimens other than serum.  
Remarks
  
Stability
Ambient: Unacceptable; Refrigerated: 5 weeks; Frozen: Indefinitely (avoid repeated freeze/thaw cycles)  
Reference Interval
Negative - Less than 2.0 U/mL
Weak Positive - 2.0-4.0 U/mL
Positive - 4.1 or greater U/mL  
Interpretive Data


See Compliance Statement B: www.aruplab.com/CS
Statement B: 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.
 
Note
For urine refer to test Histoplasma Galactomannan Antigen Quantitative by EIA, Urine (ARUP test code 2009418).
CPT Code(s)
87385
Components
Component Test Code*Component Chart NameLOINC
0060749Histoplasma Antigen, Serum6428-7
0092523Histoplasma Antigen, Serum Interp44525-4
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
  • Histoplasma antigen immunoassay
  • serum histoplasma