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Test Directory

Toxoplasma Antibodies (IgG, IgM)

Test Summary

Toxoplasmosis is a parasitic infection caused by the protozoan Toxoplasma gondii. Approximately 23% of the immunocompetent population are asymptomatic carriers of the parasite. The combination of high titers of IgG and IgM antibodies to Toxoplasma gondii is consistent with infection in the last three months. High titers of IgG and low to medium titers of IgM antibodies to Toxoplasma gondii are consistent with infection in the last three to six months.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum

Minimum Volume

0.6 mL

Instructions

N/A

Patient Preparation

N/A

Storage

Plastic screw-cap vial

Transport Temperature

Room Temperature

Specimen Stability

  • Room temperature: 4 days
  • Refrigerated: 7 days
  • Frozen: 30 days

Limitations

The U.S. Food and Drug Administration (FDA) is advising physicians that they should not use the result from any one Toxoplasma IgM commercial test kit as the sole determinant of recent Toxoplasma infection when screening a pregnant patient. Because these tests can have false-positive results, reliance on a single test result could lead to misdiagnosis, resulting in unnecessary treatment of the patient and/or termination of the pregnancy.

Other Acceptable Specimens

N/A

Unacceptable Specimens

Gross hemolysis, grossly lipemic

Order Code

TOXOGM

EPIC (Premier) Code

LAB396

Includes

Toxoplasma Antibody (IgM), Toxoplasma Antibody (IgG)

CPT Code

  • 86777
  • 86778

Billing Code

  • 670731
  • 670732

CPT Statement

Methodology

Immunoassay (IA)

FDA Status

FDA Approved

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly VA, 20153

Reference Range

Toxoplasma Antibody (IgG)
IU/mL Interpretation
<7.20 Negative
7.20-8.79 Equivocal
>8.79 Positive

Toxoplasma Antibody (IgM)
AU/mL Interpretation
<8.00 Negative
8.00-9.99 Equivocal
>9.99 Positive

Setup Schedule / Expected Turnaround Time

Tuesday, Thursday, Saturday; Report available: 2 - 5 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum

Minimum Volume

0.6 mL

Instructions

N/A

Patient Preparation

N/A

Storage

Plastic screw-cap vial

Transport Temperature

Room Temperature

Specimen Stability

  • Room temperature: 4 days
  • Refrigerated: 7 days
  • Frozen: 30 days

Limitations

The U.S. Food and Drug Administration (FDA) is advising physicians that they should not use the result from any one Toxoplasma IgM commercial test kit as the sole determinant of recent Toxoplasma infection when screening a pregnant patient. Because these tests can have false-positive results, reliance on a single test result could lead to misdiagnosis, resulting in unnecessary treatment of the patient and/or termination of the pregnancy.

Other Acceptable Specimens

N/A

Unacceptable Specimens

Gross hemolysis, grossly lipemic

Billing

CPT Code

  • 86777
  • 86778

Billing Code

  • 670731
  • 670732

CPT Statement

Result Information

Methodology

Immunoassay (IA)

Testing Laboratory

N/A

Reference Range

Toxoplasma Antibody (IgG)
IU/mL Interpretation
<7.20 Negative
7.20-8.79 Equivocal
>8.79 Positive

Toxoplasma Antibody (IgM)
AU/mL Interpretation
<8.00 Negative
8.00-9.99 Equivocal
>9.99 Positive

Setup Schedule / Expected Turnaround Time

Tuesday, Thursday, Saturday; Report available: 2 - 5 days