Strongyloides Antibody, IgG by ELISA, Serum
0099564
Ordering Recommendation
 
Mnemonic
STRONGY
Methodology
Semi-Quantitative Enzyme-Linked Immunosorbent Assay
Performed
Wed
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 or plain red.  
Specimen Preparation
Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min. 0.05 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Bacterially contaminated, heat-inactivated, hemolyzed, icteric, or lipemic specimens.  
Remarks
  
Stability
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year  
Reference Interval
1.49 IV or less: Negative - No significant level of Strongyloides IgG antibody detected.
1.50-2.10 IV: Equivocal - Questionable presence of  Strongyloides IgG antibody detected. Repeat testing in 10-14 days may be helpful.
2.11 IV or greater: Positive- IgG antibodies to Strongyloides detected, which may suggest current or past infection.  
Interpretive Data


See Compliance Statement D: www.aruplab.com/CS
Statement D: 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
 
CPT Code(s)
86682
Components
Component Test Code*Component Chart NameLOINC
0099564Strongyloides Antibody, IgG By ELISA34376-4
* 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
  • Ova and Parasite Exam
  • Strongyloides IgG