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SECTION 1.5.1 Rapid HIV 1 & 2 Antibody by OraQuick.pdf - njhiv1.org

SECTION 1.5.1 Rapid HIV 1 & 2 Antibody by OraQuick.pdf - njhiv1.org 2025

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The NJ HIV Positive Tracking Form is a document used to record the results of rapid HIV tests, including client identification, test site information, and referral to treatment. It outlines procedures for handling positive results, discordant results, and client referrals for further care. The form ensures proper documentation and follow-up for individuals tested for HIV.

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Click ‘Get Form’ to open it in the editor.
Begin by entering the Client ID number and the Date at the top of the form.
Fill in the First Test Site ID Number and Name, along with the Counselor's Name and Number.
Select the First Rapid HIV Test Type by checking 'OraQuick' or other options as applicable.
Indicate the Result of the test, marking 'Positive HIV 1/2 Antibody' if applicable.
Circle the Specimen type used: Oral, Fingerstick, or Venipuncture.
Complete the Test Kit Lot Number field with relevant information.
If a second test is required, enter details for the Second Test Site and Counselor as needed.
Follow through with any additional instructions regarding discordant results or referrals as outlined in the form.

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Versions	Form popularity	Fillable & printable
2017	4.9 Satisfied (39 Votes)
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2013	4.2 Satisfied (57 Votes)

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What is -1 and 2 antibody rapid screening test?

An 1 and 2 Antibody, Rapid Screening Test test detects the presence of antibodies in blood. These antibodies may take about 6-12 weeks (upto 6 months in some cases) to form after infection/ exposure, in detectable quantity. This period is called the window period.

How accurate is the 1 2 antibody rapid test?

It can detect 1 and 2 antibodies in whole blood, serum or plasma. This test is believed to screen with accuracy above 99% (99.99% sensitivity and 99.88% specificity according to the manufacturer) and is being used in several laboratories in Gabon [15]. Clinical diagnostic accuracy of the rapid test ACCU-TELL anti- 1 + PubMed Central articles PMC12211211 PubMed Central articles PMC12211211

How accurate is the OraQuick rapid -1 2 antibody test?

In our population, the test presents a specificity of 99.9% and a sensitivity of 93%.

How accurate is the OraQuick rapid test?

This report definitively demonstrates that the OraQuick ADVANCE Test can detect IgM antibodies during an acute infection window period of approximately 2025 days after infection, and is therefore suitable for use in testing environments requiring adherence to current CDC recommendations. Human anti- IgM detection by the OraQuick ADVANCE Rapid 1 nih.gov articles PMC5834934 nih.gov articles PMC5834934

What is OraQuick -1 2 rapid antibody test?

The OraQuicka ADVANCE Rapid -112 Antibody Test is a single-use, qualitative immunoassay to detect antibodies to Human lmmunodeliciency Virus Type 1 (-1) and Type 2 (-2) in oral fluid, fingerstick whole blood, venipuncture whole blood and plasma specimens.

How to read OraQuick test results?

Positive Result If there are two complete lines, one next to the C and any line next to the Teven a faint lineyou may have .