3. Promoting HIV Testing in Diverse Populations |
|||
Point-of-Care Testing vs Laboratory-Based TestingMost available HIV tests detect only antibodies to HIV, which, in most newly infected persons, develop and become detectable using current testing technologies at an average of at least 2 weeks following infection. [Bennett] Most HIV testing programs offer either one of 2 types of testing: point-of-care or laboratory-based. [Modica C. 2009] With point-of-care tests, the practitioner take a specimen from the patient—either oral fluid or blood—and has the test performed. With an oral fluid test, the specimen is inserted into a developing fluid, with results available in approximately 20 minutes. Specimens for such tests are simpler to collect and are more readily accepted by most patients. [White 2009] Point-of-care blood-based tests use either a finger prick or whole-blood sample produce results in 10 to 20 minutes. Currently, 4 point-of-care HIV tests—each highly sensitive and specific—have been approved for marketing (Table-I). [FDA list 2011] However, in light of the extensive implications of a positive HIV test finding, the results found with a single specimen—whether that is performed at point of care or in a laboratory—must be confirmed, generally by sending the specimen to a laboratory for further evaluation and confirmation, typically by a Western blot assay. In the case of HIV tests that are initially performed in a laboratory setting, however, performance of confirmatory testing typically is done automatically without the need for submission of a second specimen from the patient. Either of 2 different technologies is typically employed to perform laboratory-based HIV testing [Bennett]:
|
|||