The validity of HIV testing using sputum from suspected tuberculosis patients, Botswana, 2001
DESIGN: To determine the utility of the OraQuick® HIV-1/2 Assay for the detection of HIV antibodies in sputum, we consecutively enrolled adult in-patients in Botswana who had sputum sent for acid-fast bacilli testing and serum sent for HIV ELISA testing. OraQuick® HIV-1/2 Assay was applied to gingival secretions according to manufacturerÕs guidelines, and was also dipped into sputum specimens. A subset of 60 sputum specimens was also serially tested up to 72 hours after collection.
RESULTS: Of 377 patients, 84% were HIV-positive by serum ELISA. Compared with serum ELISA, the OraQuick® HIV-1/2 Assay detected HIV in gingival secretions with 98.4% sensitivity and 98.3% specificity (95%CI 97–99 and 92–100, respectively), and 97.1% sensitivity and 98.3% specificity on initial sputum specimens (95%CI 95–99 and 92–100, respectively). OraQuick® HIV-1/2 Assay performance on sputum declined slightly when tested up to 72 hours after collection.
CONCLUSIONS: When applied to sputum specimens, the OraQuick® HIV-1/2 Assay demonstrates sensitivity and specificity comparable to its intended application on gingival secretions. This novel testing method will be valuable in anonymous sentinel HIV surveillance surveys among tuberculosis patients.
Document Type: Regular Paper
Affiliations: 1: BOTUSA Project, Division of Tuberculosis Elimination, NCHSTP, Centers for Disease Control and Prevention (CDC), Dulles, Virginia, USA 2: Ministry of Health, Gaborone, Botswana 3: National Health Laboratory, Ministry of Health, Gaborone, Botswana 4: Global AIDS Program, NCHSTP, CDC, Atlanta, Georgia, USA
Publication date: August 1, 2003
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