FDA Approves OraSure Rapid HIV Test for Expanded Use With Blood Drawn Intravenously
The
FDA has approved Bethlehem, Pa.-based
OraSure Technologies' OraQuick HIV test for expanded use in hospitals using blood drawn intravenously and stored in a tube, the
Allentown Morning Call reports. The test previously could be used only with blood obtained from a finger prick (Kennedy, Allentown
Morning Call, 9/10). In February, President Bush announced a plan to expand the availability of the test, which offers results that are 99.6% accurate within 20 minutes, to more than 100,000 doctors' offices and public health clinics nationwide (
Kaiser Daily HIV/AIDS Report, 6/24). While the finger-stick method is better suited for testing in clinics, the new approval "opens up the door to a greater portion of testing" because the method is better suited for hospitals, William Bruckner, OraSure's vice president of marketing, said, according to the
Morning Call. He added that hospitals perform 12 million HIV tests annually, compared with 2.3 million performed each year in public health clinics (Allentown
Morning Call, 9/10). OraSure also said it is finishing clinical trials examining the use of oral fluid and plasma samples with the OraQuick test and expects to seek FDA approval for the use of such fluids in the "near future,"
Reuters reports (
Reuters, 9/9). According to an OraSure
release, the company has filed for FDA approval for use of the OraQuick test to detect HIV-2, a less common type of HIV found mostly in West Africa (OraSure release, 9/9).
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Reprinted with permission from kaisernetwork.org. You can view the entire Kaiser Daily HIV/AIDS Report, search the archives, or sign up for email delivery at www.kaisernetwork.org/dailyreports/hiv. The Kaiser Daily HIV/AIDS Report is published for kaisernetwork.org, a free service of the Kaiser Family Foundation, by The Advisory Board Company. © 2003 by The Advisory Board Company and Kaiser Family Foundation. All rights reserved.