Ordering Recommendation

May aid in the diagnosis of schistosomiasis caused by infection with S. mansoni, especially in travelers to endemic areas.

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation
Collect

Serum Separator Tube (SST) or Plain Red.

Specimen Preparation

Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.5 mL)

Storage/Transport Temperature

Preferred transport temp: Refrigerated. Also acceptable: Frozen

Unacceptable Conditions

Contaminated, heat-inactivated, grossly hemolyzed, or lipemic specimens.

Remarks
Stability

After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 month

Methodology

Semi-Quantitative Enzyme-Linked Immunosorbent Assay

Performed

Tue, Sat

Reported

1-6 days

Reference Interval

< 9 U Negative - No significant level of Schistosoma IgG antibody detected.
9 - 11 U Equivocal - Recommend repeat testing in 2-4 weeks with fresh sample.
>11 U Positive - IgG antibodies to Schistosoma detected, which may suggest current or past infection.

Interpretive Data

Refer to report.

Compliance Category

FDA

Note

N/A

Hotline History

N/A

CPT Codes

86682

Components

Component Test Code* Component Chart Name LOINC
3004473 Schistosoma Antibody IgG by ELISA 25757-6
* 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

  • Schistosomiasis
Schistosoma Antibody IgG by ELISA