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HIV-1 RNA, Qualitative, Real-Time PCR
Test CodeHIV1P
CPT Codes
<p>87535</p>
Preferred Specimen
Send only one of the following:
Specimen Type: Plasma EDTA
Collection Container/Type
Preferred: Lavender top (EDTA)
Acceptable: White top (PPT)
Submission Container/Tube: Plastic vial
Specimen Volume: 1.6 mL
Collection Instructions:
- Separate plasma or serum from the cells by centrifugation within 24 hours after collection.
- Transfer the specimen to a transport tube.
- Separated plasma or serum can be sent in the PPT/SST ® but cannot be shipped frozen.
Specimen Type: Serum
Collection Container/Type
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1.6 mL
Collection Instructions:
- Separate plasma or serum from the cells by centrifugation within 24 hours after collection.
- Transfer the specimen to a transport tube.
- Separated plasma or serum can be sent in the PPT/SST ® but cannot be shipped frozen.
Minimum Volume
0.8 mL
Other Acceptable Specimens
Plasma collected in a PPT potassium EDTA (white-top) tube, or EDTA (lavender-top) tube
Instructions
Separate plasma or serum from the cells by centrifugation within 24 hours after collection. Transfer the specimen to a plastic screw-cap vial.
Separated plasma or serum can be sent in the PPT/SST but cannot be shipped frozen.
Separated plasma or serum can be sent in the PPT/SST but cannot be shipped frozen.
Transport Container
Plastic screw-cap vial
Transport Temperature
Frozen
Specimen Stability
Room temperature: 72 hours
Refrigerated: 5 days
Frozen: 42 days
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Whole blood • Unspun PPT • Frozen Plasma received in plasma preparation tube (in situ) • Frozen serum received in serum separator tube (in situ)
Methodology
Real-Time Polymerase Chain Reaction
Setup Schedule
Tuesday, Thursday, Saturday
Report Available
1-5 days
Reference Range
Not detected
Clinical Significance
HIV-1 Qualitative is an in vitro nucleic acid amplification test for the qualitative detection of human immunodeficiency virus type 1 (HIV-1) RNA in human serum and plasma by PCR. The test is intended to be used as an aid in diagnosis of HIV-1 infection. Detection of HIV-1 nucleic acid is indicative of HIV-1 infection. The presence of HIV-1 nucleic acid in the plasma or serum of individuals without antibodies to HIV-1 is indicative of acute or primary HIV-1 infection. The HIV-1 Qualitative PCR may also be used as an additional test to confirm the presence of HIV-1 infection in an individual with specimens reactive for HIV-1 antibodies or antigens. The assay may also be used as an aid in the diagnosis of infection with HIV-1 in pediatric subjects and pregnant women. This assay is not intended to be used for monitoring patient status, or for screening donors of blood, plasma, or human cells, tissues, and cellular and tissue-based products (HCT/Ps) for HIV.
Performing Laboratory
Quest Diagnostics Nichols Institute 14225 Newbrook Drive Chantilly, VA 20153
Last Updated: February 17, 2023