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Beaumont Laboratory

HIV 1/2 Testing Algorithm

HTLV-III Antibodies, HIV Antibodies, HIV Ag/Ab Test, HIV Combo, HIV 1/2 Screen, HIV Screen, EPIC: LAB5766, SOFT: HIV4G

Specimen Collection Criteria

Collect: One Gold-top SST tube. (Minimum Whole Blood: 4.0 mL)

Contact the Laboratory for acceptability of other tube types.

Physician Office/Drawsite Specimen Preparation

Let SST specimens clot 30-60 minutes then immediately centrifuge to separate serum from cells. Refrigerate (2-8°C or 36-46°F) the centrifuged SST tube within two hours of collection. (Min: 2.0 mL)

Preparation for Courier Transport

Transport: Centrifuged SST tube, refrigerated (2-8°C or 36-46°F). (Min: 2.0 mL)

Rejection Criteria

  • Heat inactivated serum.
  • Severely lipemic or hemolyzed specimens.
  • Specimens that have obvious bacterial contamination.
  • Red-top tubes with serum not separated from cells within two hours of collection.


Specimen Stability for Testing:

Centrifuged SST Tubes and Microtainers® with Separator Gel
Room Temperature (20-26°C or 68-78.8°F): 2-4 hours
Refrigerated (2-8°C or 36-46°F): 7 days
Frozen (-20°C/-4°F or below): Unacceptable

Red-top Tubes and Microtainers® without Separator Gel
Room Temperature (20-25°C or 68-77°F): 2-4 hours
Refrigerated (2-8°C or 36-46°F): Unacceptable
Frozen (-20°C/-4°F or below): Unacceptable

Serum Specimens (Pour-Overs)
Room Temperature (20-26°C or 68-78.8°F): 72 hours
Refrigerated (2-8°C or 36-46°F): 7 days
Frozen (-20°C/-4°F or below): 7 days

Specimen Storage in Department Prior to Disposal:

Refrigerated (2-8°C or 36-46°F): 7 days


Royal Oak Automated Chemistry Laboratory.


Sunday - Saturday, 24 hours a day.
Negative results available within 24 hours.
Positive results for HIV-1 Antibodies available within 24 hours.
If sendout testing for HIV-1 RNA or additional testing for HIV-2 is necessary, results may take an additional week. See algorithm below.

Reference Range


Test Methodology

Chemiluminescence Immunoassay.


  • A negative test result does not rule out the possibility of exposure to, or infection with, HIV.
  • An initial positive screen will be followed by confirmation testing (see algorithm below) and an interpretative report summarizing results of all tests will be issued.

Clinical Utility

The initial screen is a 4th generation assay that detects both HIV-1 p24 antigen and antibodies to HIV-1 (groups M and O) and HIV-2. The new screen will detect acute HIV infection, on average 7 to 10 days earlier than the previously used antibody-only screen.

Positive screen confirmation antibody testing to distinguish HIV-1 from HIV-2 will be performed in-house within 24 hours of initial testing. Western blots (currently a send-out test) will no longer be ordered. Rarely, additional molecular-based confirmation testing for HIV-1 and/or HIV-2 will be performed (Send Out) as delineated in the algorithm below. All test results will be included in a single report with a final interpretation.

HIV-1 IgG is first detectable 3-12 weeks after infection in nearly all cases except neonates. Once established, HIV antibody levels usually persist throughout the lifetime of the patient. The presence of antibody does not imply immunity to the virus but rather, that the patient is assumed to be infected, and infectious. (3) Little is known about the antibody response to HIV-2 infection. The response is presumed to be similar to HIV-1. (3)

Clinical Disease

Primary HIV infections are symptomatic in 50-70% of patients. These patients present with a variety of symptoms including Influenza-like or mononucleosis-like illness to more severe neurological symptoms. These symptoms may persist for a few days or up to two months. Rapid progression to AIDS is seen in patients that experience a longer acute illness. Most patients however, remain asymptomatic for 1 to greater than 10 years before the clinical symptoms of AIDS present. (2)

Disease Reporting

This is a reportable infection and positive results will be reported to the Oakland County Health Department. In Michigan, both physicians and laboratories are responsible for reporting AIDS/HIV respectively. For more information on reportable diseases, contact the Epidemiology Department at (248) 551-4040.


HIV-1 caused a worldwide pandemic of acquired immunodeficiency syndrome and AIDS-related complex. (1) In 1995, the World Health Organization estimated that 18 million adults and 1.5 million children are infected with HIV resulting in 4.5 million AIDS cases worldwide. (1)

Incubation Period

The median time from HIV infection to AIDS is 8-10 years. Homosexual men and some neonates may progress to AIDS more rapidly than other groups. (1)


HIV-1 is transmitted by blood, blood products, and body fluids. Major modes of HIV-1 transmission include sexual intercourse, parenteral transmission through shared or inadequately sterilzed needles, transfusion of HIV-1 infected blood and blood factor concentrates, and mother-to-child transmission either in utero, at birth, or through breast feeding. (1)


  1. CDC. 2006. The global HIV/AIDS pandemic, 2006. MMWR. 55: 841-844.
  2. CDC. 2006. Epidemiology of HIV/AIDS---United States. 1981-2005. MMWR. 55: 589-592.
  3. Schusbach, J. 2003. Human Immunodeficiency viruses. Manual of Clinical Microbiology, 8th edition. P.R. Murray et al. (eds). ASM Press. Washington, D.C., pp. 1253-1281.

CPT Code

Initial Screen: 87389.
If screen is positive: 86701, 86702.
Further confirmation testing (if necessary): 87535, 87538.

Test Codes


Last Updated


Microtainer® and Vacutainer® are registered trademarks of Becton, Dickinson and Company.
UroVysion® is a registered trademark of Abbott Laboratories. ThinPrep® is a registered trademark of Hologic, Incorporated.

This directory currently reflects information only for specimens collected and/or processed at the Farmington Hills, Grosse Pointe, Royal Oak, and Troy campuses.