We report a prospective comparison of human immunodeficiency virus type 1 testing by enzyme immunoassay and Western blot with four rapid tests of 486 subjects performed in rural Kenya. Rapid test sensitivity was 100%. Specificity ranged from 99.1 to 100%. Combined use of two Food and Drug Administration-approved rapid tests yielded a single false-positive result.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC497567 | PMC |
http://dx.doi.org/10.1128/JCM.42.8.3850-3852.2004 | DOI Listing |
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