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
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.
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)
|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.
No compliance statements are in use for this test.
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 IgM
- TORCH Profile IgM
- Toxoplasma gondii (T. gondii)