Torch Antibodies, IgM




Test Mnemonic

TORCHM

CPT Codes

  • 86762 - QTY (1)
  • 86694 - QTY (1)
  • 86778 - QTY (1)
  • 86645 - QTY (1)

Includes

  • Rubella IgM
  • CMV IgM
  • Toxoplasma IgM
  • HSV Types 1/2 IgM Abs

Performing Laboratory

ARUP


Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
2 mLSerumSST (Gold) RefrigeratedAllow specimen to clot completely at room temperature. Separate from cells ASAP or within 2 hours of collection and transfer to standard aliquot tube. Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Label specimens plainly as 'acute' or 'convalescent.'

Minimum Specimen Requirements

Volume Type Container Collect Temperature Transport Temperature Special Instructions
1 mL     

Stability

Environmental Condition Description
FrozenAfter separation from cells: 1 year (Avoid repeated freeze/thaw cycles)
AmbientAfter separation from cells :2 days
RefrigeratedAfter separation from cells: 2 weeks

Days Performed

Sun - Sat

Turnaround Time

2 - 3 days

Methodology

Name Description
Semi Quantitative Enzyme Linked Immunosorbent Assay 
Semi-Quantitative Chemiluminescent Immunoassay 

Reference Range

CMV IgM
Sex Age From Age To Type Range Range Unit
   Years99 YearsNormal<= 29.9 Not DetectedAU/mL
   Years99 YearsNormal30.0 - 34.9 IndeterminateAU/mL
   Years99 YearsNormal>= 35.0 DetectedAU/mL
HSV Types 1/2 IgM Abs
Sex Age From Age To Type Range Range Unit
   Years99 YearsNormal<= 0.89 Not DetectedIV
   Years99 YearsNormal0.90 - 1.09 IndeterminateIV
   Years99 YearsNormal>= 1.10 DetectedIV
Rubella IgM
Sex Age From Age To Type Range Range Unit
   Years99 YearsNormal<= 19.9 Not DetectedAU/mL
   Years99 YearsNormal20.0 - 24.9 IndeterminateAU/mL
   Years99 YearsNormal>= 25.0 DetectedAU/mL

Special Info

Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. This test is New York DOH approved.

Clinical Info

This test is not recommended for diagnosing congenital infections in newborns; tests should be selected individually to target the most likely infectious agents.