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HIV Antibodies, HIV-1/-2, EIA, with Reflexes

Test Code

19728X

CPT Code(s)

86703

For New York patient testing, use test code 17659X

Includes

If the HIV-1/HIV-2 EIA Antibody Screen is reactive, HIV-1 Antibody Western Blot will be performed at an additional charge (CPT code(s): 86689).

If the HIV-1 Antibody, Western Blot is negative or indeterminate, HIV-2 Antibody EIA will be performed at additional charge (CPT code(s): 86702).

If the HIV-2 Antibody EIA is reactive, HIV-2 Antibody Western Blot will be performed at an additional charge (CPT code(s): 86689).



This reflexing algorithm is consistent with CDC/FDA recommendations.



The HIV-1/2 EIA Antibody Screen includes testing for HIV-1 Group O.

Preferred Specimen(s)

2 mL serum

Minimum Volume

1 mL

Alternative Specimen(s)

Plasma collected in an EDTA (lavender-top), EDTA (royal blue-top), sodium heparin (green-top), lithium heparin (green-top), 3.2% sodium citrate (light blue-top) or ACD solution B (yellow-top) tube

Collection Instructions

To protect patient confidentiality, we recommend identifying specimens by using a code number in place of patients name on the specimen vial and the test request form. Tube must be labeled with patient identifier and submitted only for HIV testing. HIV-1 Western Blot requires the original tube for testing.

Transport Temperature

Room temperature

Specimen Stability

Room temperature: 7 days

Refrigerated: 14 days

Frozen: 30 days

Methodology

Immunoassay

Performing Laboratory

Quest Diagnostics Nichols Institute

33608 Ortega Highway

San Juan Capistrano, CA 92690-6130

Setup Schedule

Set up: Tues-Sat; Report available: 2-5 days

Limitations

HIV antibodies may not be detected in window between infection and detection of antibody.

Reference Range(s)

HIV-1/2 Ab Screen, EIA Non-Reactive

A Nonreactive HIV-1/2 antibody result does not exclude HIV infection since the time frame for seroconversion is variable. If acute HIV infection is suspected, antibody retesting and nucleic acid amplification (HIV DNA/RNA) testing is recommended

Clinical Significance

The combination HIV-1/HIV-2 includes detection of subtypes of HIV-1 not included in HIV-1, EIA alone. Repeatedly positive results are confirmed by the highly specific western blot.

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

(The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.)

* The tests listed by specialist are a select group of tests offered. For a complete list of Quest Diagnostics tests, please refer to our Directory of Services.