Aid in the diagnosis of Strongyloides infection. Positive results in patients from endemic areas may not represent active infection.
Semi-Quantitative Enzyme-Linked Immunosorbent Assay
New York DOH Approval Status
Serum Separator Tube (SST) or Plain Red.
Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min. 0.3 mL)
Bacterially contaminated, heat-inactivated, hemolyzed, icteric, or lipemic specimens.
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
Effective August 20, 2018
|0.9 IV or less||Negative - No significant level of Strongyloides IgG antibody detected.|
|1.0 IV||Equivocal - The Strongyloides IgG antibody result is borderline and therefore inconclusive. Recommend retesting the patient in 2-4 weeks, if clinically indicated.|
|1.1 IV or greater||Positive - IgG antibodies to Strongyloides detected, which may suggest current or past infection.|
False-positive results may occur with prior exposure to other helminth infections. Testing low-prevalence populations may also result in false-positive results.
|Component Test Code*||Component Chart Name||LOINC|
|0099564||Strongyloides Antibody, IgG By ELISA||34376-4|
- Ova and Parasite Exam
- Strongyloides IgG