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Journal of Clinical Microbiology, 11 1995, 2899-2902, Vol 33, No. 11
WJ Kassler, C Haley, WK Jones, AR Gerber, EJ Kennedy and JR George
Rapid, on-site human immunodeficiency virus (HIV) testing has the potential
to improve the delivery of prevention services in publicly funded
counseling and testing sites. The Single Use Diagnostic System (SUDS) HIV-1
is the only rapid enzyme immunoassay (EIA) approved for diagnostic use in
the United States. To evaluate the feasibility of using SUDS in public
clinics and to validate the test's performance in a public health
laboratory, we conducted blinded SUDS testing on plasma sent for HIV
testing. From 19 March through 30 June 1993, 1,923 consecutive samples from
a sexually transmitted diseases clinic and an HIV counseling and testing
clinic were tested on site with SUDS. Tests done in the first two weeks
with a malfunctioning centrifuge n = 402) and those done when there were
excessively high temperatures in the laboratory (n = 53) were analyzed
separately. Of 1,466 tests, 39 were positive by both SUDS and EIA (with
Western blot [immunoblot] confirmation) and 7 were SUDS positive and EIA
negative. Western blotting was used as the "gold standard" to adjudicate
these discrepancies. There were no SUDS-negative and EIA-positive tests.
Compared with that of EIA (with Western blot confirmation), the sensitivity
of SUDS was 100% (95% confidence interval, 88.8 to 100%) and the
specificity was 99.5% (95% confidence interval, 98.9 to 99.8%). The
positive predictive value of SUDS was 88% in the STD clinic and 81% in the
HIV counseling and testing clinic. There was a 7.7-fold increase in false
positives, from 0.48 to 3.7%, when there was inadequate centrifugation and
when the temperature exceeded the manufacturer's recommendations. Rapid,
on-site HIV testing by the SUDS assay is feasible and practical in public
health settings. The test can be performed accurately, at reasonable cost,
and within the time frame of a typical clinic visit. Caution should be
used, however, as two conditions adversely affected the accuracy of this
test: inadequate specimen preparation and elevated temperature.
Copyright © 1995 by the American Society for Microbiology. All rights reserved.
Performance of a rapid, on-site human immunodeficiency virus antibody assay in a public health setting
Division of STD/HIV Prevention, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
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