10-6046-0 HIV101 Stat-Pak Tri-lingual Rev 17[1] - Aides Et Hiv

Can prep clinicians manage ambiguous HIV test results during follow-up visits?

A strategy for PrEP clinicians to manage ambiguous HIV test results during follow-up visits. Open Forum Infect Dis. 2018;5 (8):ofy180.

How accurate is stat-Pak?

Evaluation of the STAT-PAK RDT in plasma during the second year resulted in a sensitivity of 99.7% (99.1 to 99.9%) and a specificity of 99.3% (99.1 to 99.4%) with 6.9% of the positive results being false.

What is a who prequalified HIV-1 and HIV-2 assay?

A WHO Prequalified, rapid point-of-care assay for the detection of HIV-1 and HIV-2 antibodies in fingerstick whole blood, venous whole blood, serum or plasma. No Debug Key available as Do Not Track is enabled. This opens in a new window.

What is stat-Pak test?

STAT-PAK HIV1/2, kit/20, is a rapid immunochromatographic assay, for the detection of antibodies to HIV Types 1 and 2 (HIV 1/.
2) Technical specifications: Technology: Rapid immunochromatographic assay.
Format: Lateral flow cassette, 20 tests.
Sample type: Whole blood, serum, plasma.

What is the differential diagnosis of acute HIV infection?

The differential diagnosis of acute HIV infection may include, but is not limited to, viral illnesses, such as COVID-19, EBV and non-EBV (e.g., CMV) infectious mononucleosis syndromes, influenza, viral hepatitis, streptococcal infection, or syphilis. Diagnosis of any STI should prompt HIV testing and consideration of acute HIV infection.

Who can use the ChemBio HIV 1/2 Stat-paktm test?

The Chembio HIV 1/2 STAT-PAKTM Assay is approved for use only by an agent of a clinical laboratory. Test subjects must receive the “Subject Information Notice” prior to specimen collection and appropriate information when test results are provided.

If Determine test strip indicates positive, the results has to be confirmed by a second line rapid test kit called Unigold.
If the Unigold indicates positive, the test results is concluded as positive and is given to the patients.