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Performance of the OraQuick Rapid Antibody Test for Diagnosis of Human Immunodeficiency Virus Type 1 Infection in Patients with Various Levels of Exposure to Highly Active Antiretroviral Therapy
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---3July 20242023/2024A+
- Point-of-care human immunodeficiency virus (HIV) diagnosis has advantages over conventional testing in time-critical 
settings (1–3, 5, 6, 8, 11, 12). The OraQuick HIV type 1 
(HIV-1) rapid antibody test (OraQuick; OraSure Technologies, Bethlehem, Pa.), is designed as a rapid test that uses oral 
mucosal transudate (OMT), whole blood, serum, or plasma. It 
was approved by the U.S. Food and Drug Administration in 
November 2002 for HIV-1 diagnosis by using finger-stick 
whole blood. OraQuick ...
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