| Next >
Table of Contents
Diagnostic HIV laboratory tests and interpretation algorithms evolve; individual laboratories have internal protocols for reporting tests with preliminary results. Indeterminate, inconclusive, non-diagnostic, and pending validation are among the terms used when preliminary results cannot be classified definitively. The clinician should contact the appropriate laboratory authority to determine the significance of the non-definitive results and the supplemental testing that would be indicated. This is of particular importance with tests from pregnant women, newborn children, and patients with suspected acute HIV infection or HIV-2. Clinicians should become familiar with the internal test-reporting policies of their institutions.
|Important Note (October 2013)|
A new HIV diagnostic testing algorithm has been verified through scientific studies and offers several advantages over the traditional enzyme immunoassay (EIA)-Western blot algorithm, including earlier and more accurate detection of HIV infections, the ability to differentiate between HIV-1 and HIV-2 infections, and lower costs. Recommendations for its use are anticipated from the Centers for Disease Control and Prevention (CDC). The New York State Department of Health (NYSDOH) has issued a Dear Colleague letter to update clinicians about this new algorithm. This guideline is currently in the process of being updated to include information regarding the new algorithm.
|Important Notes (June 2013)|
|Key to Abbreviated Terms|
|bDNA||Branched chain DNA|
|CDC||Centers for Disease Control and Prevention|
|ELISA||Enzyme-linked immunosorbent assay|
|FDA||US Food and Drug Administration|
|HLA||Human leukocyte antigen|
|NAT||Nucleic acid test|
|OMT||Oral mucosal transudate|
|PBMC||Peripheral blood mononuclear cell|
|PCR||Polymerase chain reaction|
Technologic advances in HIV laboratory testing continue to aid in screening, diagnosis, and patient management. Effective methods for detection of HIV-related laboratory markers are critical for both accurate HIV screening and for monitoring patients for disease progression and viral resistance to therapy. This chapter provides an overview of currently available HIV laboratory screening methods, viral load assays, and HIV resistance tests. Many new technologies that will further enhance testing methods are in various stages of development.
Patients presenting for testing within 36 hours of exposure to HIV should be assessed for post-exposure prophylaxis (see Post-Exposure Prophylaxis Guidelines). Expert advice may be obtained from the National Clinicians' Consultation Center PEP Line at 1-888-HIV-4911 (1-888-448-4911).
| Next >
(Please note: Your name and comment will be public, and may even show up in
Internet search results. Be careful when providing personal information! Before
adding your comment, please read TheBody.com's Comment Policy