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Test Directory

Quanti-FERON® TB-Gold

Test Summary

The QuantiFERON test is based upon a cell-mediated immune response in TB-infected individuals. The T cells of the patient are stimulated with Mycobacterium tuberculosis antigens. If the patient has previously been exposed to Mycobacterium tuberculosis, the exposure to these antigens in the QuantiFERON assay stimulate the patient's T cells to secrete the cytokine interferon-γ. The presence of the interferon-γ is then detected using an EIA method. According to the CDC, this assay may be used as a substitute for a TB skin test. It is more specific than the TB skin test, will detect latent TB, and a positive result is obtained in about 85% of the patients with active TB.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

QuantiFERON In-Tube collection tubes required.
In-Tube collection tubes are a set 4 tubes that are used specifically for collection for Quanti-FERON® TB-Gold testing.

Minimum Volume

N/A

Instructions

NOTE: Outpatients from a doctor's office must go to a PSC to have the sample collected.
Hospitalized patients will be drawn by the phlebotomy staff at the hospital.

QuantiFERON(TM)In-Tube collection tubes REQUIRED. In-Tube collection tubes are a set 4 tubes that are used specifically for collection for QuantiFERON(TM) testing.

Draw blood in all 4 tubes, shake vigorously (until frothy), and send to laboratory at room temperature (DO NOT REFRIGERATE). Must be processed within 16 hours of collection.
DO NOT SPIN THE TUBES

Patient Preparation

N/A

Storage

Quanti-FERON® TB-Gold in-tube collection tubes

Transport Temperature

Room Temperature

Specimen Stability

  • Room Temperature = 16 hours
  • Refrigerated = unacceptable
  • Frozen = unacceptable

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Reject specimen if older than 16 hours post collection, refrigerated or frozen

Order Code

QTF

EPIC (Premier) Code

LAB1401

Includes

N/A

CPT Code

  • 86480

Billing Code

  • 300553

CPT Statement

Methodology

Lymphocyte Stimulation with Immunoassay

FDA Status

FDA Approved

Physician Attestation of Informed Consent

N/A

Testing Laboratory

CompuNet Clinical Laboratories, LLC
2308 Sandridge Drive
Moraine OH, 45439

Department

Molecular/Serology

Reference Range

A positive and negative control are performed with each patient sample.
If these controls are within the acceptable limits, any value <0.35 IU/ML is interpreted as negative and any value >=0.35 IU/ML is interpreted as positive. If the positive and negative control are outside the acceptable limits, the results are interpreted as indeterminate.

Setup Schedule / Expected Turnaround Time

Collect Samples: Monday - Sunday. Testing Performed: Tuesday, Thursday, and Saturday or Sunday; BS; Report available: 4 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

QuantiFERON In-Tube collection tubes required.
In-Tube collection tubes are a set 4 tubes that are used specifically for collection for Quanti-FERON® TB-Gold testing.

Minimum Volume

N/A

Instructions

NOTE: Outpatients from a doctor's office must go to a PSC to have the sample collected.
Hospitalized patients will be drawn by the phlebotomy staff at the hospital.

QuantiFERON(TM)In-Tube collection tubes REQUIRED. In-Tube collection tubes are a set 4 tubes that are used specifically for collection for QuantiFERON(TM) testing.

Draw blood in all 4 tubes, shake vigorously (until frothy), and send to laboratory at room temperature (DO NOT REFRIGERATE). Must be processed within 16 hours of collection.
DO NOT SPIN THE TUBES

Patient Preparation

N/A

Storage

Quanti-FERON® TB-Gold in-tube collection tubes

Transport Temperature

Room Temperature

Specimen Stability

  • Room Temperature = 16 hours
  • Refrigerated = unacceptable
  • Frozen = unacceptable

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Reject specimen if older than 16 hours post collection, refrigerated or frozen

Billing

CPT Code

  • 86480

Billing Code

  • 300553

CPT Statement

Result Information

Methodology

Lymphocyte Stimulation with Immunoassay

Testing Laboratory

N/A

Reference Range

A positive and negative control are performed with each patient sample.
If these controls are within the acceptable limits, any value <0.35 IU/ML is interpreted as negative and any value >=0.35 IU/ML is interpreted as positive. If the positive and negative control are outside the acceptable limits, the results are interpreted as indeterminate.

Setup Schedule / Expected Turnaround Time

Collect Samples: Monday - Sunday. Testing Performed: Tuesday, Thursday, and Saturday or Sunday; BS; Report available: 4 days