Not recommended for diagnosing congenital infections in newborns; tests should be selected individually to target the most likely infectious agents.
Semi-Quantitative Chemiluminescent Immunoassay/Semi-Quantitative Enzyme-Linked Immunosorbent Assay
Sun-Sat
1-2 days
Serum Separator Tube (SST).
Allow specimen to clot completely at room temperature. Separate from cells ASAP or within 2 hours of collection. Transfer 2 mL serum to an ARUP Standard Transport Tube. (Min: 1 mL) Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens.
Refrigerated.
Mark specimens plainly as "acute" or "convalescent."
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)
Test Number |
Components |
Reference Interval |
||||||
---|---|---|---|---|---|---|---|---|
0050553 | Cytomegalovirus Antibody, IgM |
|
||||||
0050641 | Herpes Simplex Virus Type 1 and/or 2 Antibodies, IgM by ELISA |
|
||||||
0050551 | Rubella Antibody, IgM |
|
||||||
0050557 | Toxoplasma gondii Antibody, IgM |
|
||||||
Refer to report.
FDA
This test should not be used for blood donor screening, associated re-entry protocols, or for screening Human Cell, Tissues and Cellular and Tissue-Based Products (HCT/P).
86645; 86694; 86762; 86778
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0050551 | Rubella Antibody IgM | 5335-5 |
0050553 | CMV Antibody IgM | 7853-5 |
0050557 | Toxoplasma gondii Ab, IgM | 8040-8 |
0050641 | HSV 1 and/or 2 Abs, IgM by ELISA | 41399-7 |
- Cytomegalic Inclusion Disease (CMID)
- Cytomegalovirus (CMV)
- Herpes Simplex Virus (HSV)
- TORCH
- TORCH IgM
- TORCH Profile IgM
- Toxoplasma gondii (T. gondii)
- Toxoplasmosis