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Bioline hiv 1 2 3

Manufactured by Standard Diagnostics

The Bioline® HIV 1/2 3.0 is an in-vitro diagnostic device for the qualitative detection of antibodies to Human Immunodeficiency Virus Type 1 (HIV-1) and Type 2 (HIV-2) in human serum or plasma samples.

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2 protocols using bioline hiv 1 2 3

1

HIV Rapid Testing in South Sudan

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Trained counselors used finger prick to conduct HIV rapid tests, following South Sudan’s national HIV testing guidelines at the time; parallel tests used Uni-Gold Recombigen® HIV (Trinity Biotech, Bray Country, Ireland) and Determine® HIV 1/2 (Inverness Medical Innovations, Petchabun, Japan) tests. Bioline® HIV 1/2 3.0 (Standard Diagnostics, Inc., Korea) was used as a tiebreaker for discordant results.
Dried blood spot samples drawn by lancet from the finger were collected for HIV rapid test QC, malaria and VL testing in 2010, and syphilis testing in 2012, and storage for future testing.
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2

Baseline HIV Testing and Confirmation

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During the baseline assessment, we asked the 209 participants about their engagement in HIV care, including whether they had 1) ever received an HIV screening test and 2) received their confirmatory test result. Data was collected through computer-assisted personal interviewing (CAPI) programmed with Epi Info 7 (Centers for Disease Control and Prevention, Atlanta, GA, USA). This information is presented in Results 1 and Figure 1.
During the baseline assessment, all participants were tested for HIV through rapid HIV testing using a finger-stick blood specimen (Bioline HIV 1/2 3.0, Standard Diagnostics, Korea) followed by confirmatory testing with HIV-1 antibody immunofluorescence assay (IFA) for reactive rapid tests.
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