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Test Directory

HIV-1 Genotype (RTI, PI, Integrase Inhibitors)

Test Summary

Identify drug resistance mutations in HIV-1 patients failing antiretroviral regimens containing RT, PR or Integrase inhibitors.
Identify transmitted drug resistance mutations in the RT, PR or integrase genes in treatment-naive patients prior to initiation of antiretroviral therapy.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

4 mL plasma collected in an EDTA (lavender top) or PPT (white top) tube

Minimum Volume

1.2 mL

Instructions

Do not freeze whole blood or any samples stored in primary tube. Freshly drawn specimens (whole blood) may be stored at 2-25°C for up to 24 hours prior to centrifugation. Separate plasma from cells within 24 hours of collection by centrifugation. If shipping frozen, transfer plasma to a leak-proof transport tube, then freeze prior to shipment. Follow manufacturer's instructions for collection tube handling.

Patient Preparation

N/A

Storage

Transport tube

Transport Temperature

Frozen

Specimen Stability

  • Room temperature: 24 hours
  • Refrigerated: 6 days
  • Frozen: 42 days

Limitations

N/A

Other Acceptable Specimens

CSF collected in a sterile leak-proof container

Unacceptable Specimens

Plasma received frozen in the plasma preparation tube (PPT) • Serum • Whole blood greater than 24 hours old • Frozen whole blood

Order Code

HIVING

EPIC (Premier) Code

LAB6186

Includes

HIV-1 Integrase Genotype
HIV-1 Genotype

CPT Code

  • 87900
  • 87901
  • 87906

Billing Code

  • 671013
  • 670002
  • 670001

CPT Statement

Methodology

Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) • Sequencing

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
33608 Ortega Highway
San Juan Capistrano CA, 92675

Department

Reference Testing

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Monday - Saturday; Report available: 4 - 9 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

4 mL plasma collected in an EDTA (lavender top) or PPT (white top) tube

Minimum Volume

1.2 mL

Instructions

Do not freeze whole blood or any samples stored in primary tube. Freshly drawn specimens (whole blood) may be stored at 2-25°C for up to 24 hours prior to centrifugation. Separate plasma from cells within 24 hours of collection by centrifugation. If shipping frozen, transfer plasma to a leak-proof transport tube, then freeze prior to shipment. Follow manufacturer's instructions for collection tube handling.

Patient Preparation

N/A

Storage

Transport tube

Transport Temperature

Frozen

Specimen Stability

  • Room temperature: 24 hours
  • Refrigerated: 6 days
  • Frozen: 42 days

Limitations

N/A

Other Acceptable Specimens

CSF collected in a sterile leak-proof container

Unacceptable Specimens

Plasma received frozen in the plasma preparation tube (PPT) • Serum • Whole blood greater than 24 hours old • Frozen whole blood

Billing

CPT Code

  • 87900
  • 87901
  • 87906

Billing Code

  • 671013
  • 670002
  • 670001

CPT Statement

Result Information

Methodology

Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) • Sequencing

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Monday - Saturday; Report available: 4 - 9 days