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Mayo Test Catalog, (Sorted By Test Name) - Mayo Medical ...

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HV1CD<br />

83628<br />

HIV antibody test results. However, a negative HIV-1 antibody WB result does not exclude the<br />

possibility of early HIV-1 or HIV-2 infection. If the HIV-1 antibody WB test result is negative, the<br />

HIV-2 antibody test by EIA will be performed automatically (at an additional charge). Indeterminate<br />

HIV-1 antibody WB results occur when bands are present but the patterns do not meet the criteria for a<br />

positive result. Indeterminate results may indicate a) early, late, or incomplete HIV-1 antibody<br />

reactivity, b) presence of HIV-2 antibodies, or c) presence of non-specific cross-reactive antibodies. For<br />

specimens with indeterminate WB results, confirmatory HIV-1 antibody testing by IFA) and HIV-2<br />

antibody testing by EIA will be performed automatically (at additional charges). Indeterminate WB<br />

patterns can be found in up to 15% of persons without evidence of HIV infection. Individuals with<br />

persistent, stable, indeterminate HIV-1 antibody WB results but without risk factors should be<br />

monitored for 6 months. If no additional WB bands develop during that time, the patient is determined<br />

not to be HIV-infected. An uninterpretable HIV-1 antibody WB result indicates the presence of smear<br />

or blotches obscuring proper reading of the WB strip, in the absence of discrete bands. Such findings<br />

indicate probable nonspecific binding of antibodies in the patientâ€s serum to the WB strip. For<br />

specimens with such uninterpretable WB results, confirmatory HIV-1 antibody test by IFA and HIV-2<br />

antibody testing by EIA will be performed automatically (at additional charges). See HIV Rapid<br />

Serology Follow-up Algorithm in Special Instructions.<br />

Reference Values:<br />

Negative<br />

See HIV Serologic Interpretive Guide in Special Instructions for further interpretive information.<br />

Clinical References: 1. Center for Disease Control and Prevention: Protocols for confirmation of<br />

reactive rapid HIV tests. MMWR Morb Mortal Wkly Rep 2004;53:221-222 2. Branson BM, Handsfield<br />

HH, Lampe MA: Center for Disease Control and Prevention: Revised recommendations for HIV testing<br />

of adults, adolescents, and pregnant women in health-care settings. MMWR Recomm Rep 2006;55:1-17<br />

3. Constantine N: HIV antibody assays May 2006. HIV InSite Knowledge Base (online textbook);<br />

Available from URL: http://hivinsite.ucsf.edu/InSite?page=kb-00&doc=kb-02-02-01 4. Owen SM, Yang<br />

C, Spira T: Alternative algorithms for human immunodeficiency virus infection diagnosis using tests that<br />

are licensed in the United States. J Clin Microbiol 2008;46:1588-1595<br />

HIV-1 and HIV-2 Antibodies for Cadaveric or Hemolyzed<br />

Specimens, Serum<br />

Clinical Information: Epidemiological data indicate that AIDS is caused by at least 2 types of HIV.<br />

The first virus, HIV-1, has been isolated from patients with AIDS, AIDS-related complex, and<br />

asymptomatic infected individuals at high risk for AIDS. HIV-1 is transmitted by sexual contact, exposure<br />

to infected blood or blood products, or from an infected mother to her fetus or infant. A second HIV virus,<br />

HIV-2, was isolated from patients in West Africa in 1986. HIV-2 appears to be endemic only in West<br />

Africa, but it also has been identified in individuals who have lived in West Africa or had sexual relations<br />

with individuals from that geographic region. HIV-2 is similar to HIV-1 in its morphology, overall<br />

genomic structure, and its ability to cause AIDS. Antibodies against HIV-1 and HIV-2 are usually not<br />

detected until 6 to 12 weeks following exposure and are almost always detected by 12 months. They may<br />

fall into undetectable levels in the terminal stage of AIDS. See HIV <strong>Test</strong>ing Algorithm (excludes HIV<br />

rapid testing) and HIV Rapid Serology Follow-up <strong>Test</strong>ing Algorithm in Special Instructions.<br />

Useful For: Diagnosis of HIV-1 and/or HIV-2 infection in cadaveric or hemolyzed serum specimens<br />

from symptomatic patients with or without risk factors for HIV infection (assay kit is FDA-approved for<br />

testing cadaveric or hemolyzed blood specimens)<br />

Interpretation: A reactive HIV-1/-2 antibody screen result obtained by EIA suggests the presence of<br />

HIV-1 and/or HIV-2 infection. However, it does not differentiate between HIV-1 and HIV-2 antibody<br />

reactivity. Confirmatory testing by HIV-1 antibody-specific Western blot (WB) or immunofluorescence<br />

assay is necessary to verify the presence of HIV-1 infection. The presence of HIV-2 infection is screened<br />

by HIV-2 antibody-specific EIA with confirmation by HIV-2 antibody-specific immunoblot assay. All<br />

EIA-reactive specimens tested will automatically be tested by WBAR/23878 HIV-1/-2 Antibody<br />

Confirmatory Evaluation, Serum at an additional charge. Please see the individual unit code for<br />

Current as of January 3, 2013 2:22 pm CST 800-533-1710 or 507-266-5700 or <strong>Mayo</strong><strong>Medical</strong>Laboratories.com Page 946

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