HIV-1 RNA, Quantitative, Real-Time PCR, CSF
Test Summary
This test is intended for use in conjunction with clinical presentation and other laboratory markers of disease progress for the clinical management of HIV-1 infected patients. The test can be used to assess patient prognosis by measuring the baseline HIV-1 RNA level or to monitor the effects of antiretroviral therapy by measuring changes in EDTA plasma HIV-1 RNA levels during the course of anti-retroviral treatment.
Aliases
- N/A
Specimen Collection
Special Instructions
Preferred Specimen
Minimum Volume
Instructions
Patient Preparation
Storage
Transport Temperature
Specimen Stability
- Room temperature: 24 hours
- Refrigerated: 5 days
- Frozen: 35 days
Limitations
Other Acceptable Specimens
Unacceptable Specimens
Order Code
EPIC (Premier) Code
Includes
CPT Code
- 87536
Billing Code
- 670051
CPT Statement
Methodology
FDA Status
Physician Attestation of Informed Consent
Testing Laboratory
33608 Ortega Highway
San Juan Capistrano CA, 92675
Department
Reference Range
- HIV-1 RNA, QN PCR, CSF Not Detected
- d HIV-1 RNA, QN PCR, CSF Not Detected
This test was performed using the Cobas® AmpliPrep/Cobas® Taqman® HIV-1 test kit version 2.0 (Roche Molecular Systems, Inc.) Use of this test on CSF specimen is a modification of the test's intended use.
Setup Schedule / Expected Turnaround Time
Specimen Collection
Special Instructions
Preferred Specimen
Minimum Volume
Instructions
Patient Preparation
Storage
Transport Temperature
Specimen Stability
- Room temperature: 24 hours
- Refrigerated: 5 days
- Frozen: 35 days
Limitations
Other Acceptable Specimens
Unacceptable Specimens
Result Information
Methodology
Testing Laboratory
Reference Range
- HIV-1 RNA, QN PCR, CSF Not Detected
- d HIV-1 RNA, QN PCR, CSF Not Detected
This test was performed using the Cobas® AmpliPrep/Cobas® Taqman® HIV-1 test kit version 2.0 (Roche Molecular Systems, Inc.) Use of this test on CSF specimen is a modification of the test's intended use.