We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

LabMedica

Download Mobile App
Recent News Expo Medica 2024 Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

Low-Cost Point-of-Care Test Monitors HIV Treatment

By LabMedica International staff writers
Posted on 03 Jun 2009
Scientists developed a prototype low-cost HIV monitoring test designed for field use in remote settings.

Developed by Australian scientists, the new test enables patients at the point of care to find out within 30 minutes if they should begin antiretroviral treatment, without any laboratory equipment being required.

The Burnet Institute (Melbourne, Australia) was awarded a grant by The CD4 Initiative for the development of a low cost, rapid point-of-care CD4+ T-cell test, specifically designed for field use in remote settings. Professor Suzanne Crowe, Associate Professor David Anderson, and senior scientist Mary Garcia lead the team at Burnet, which has expertise in diagnostic test development.

The CD4 rapid test, similar in design to a home pregnancy test, works with a finger-prick blood sample to measure the numbers of CD4+ T-cells in a person's blood. CD4+ T-cells are critical for healthy functioning of the immune system and are slowly destroyed during the course of HIV infection. When the numbers of CD4+ T-cells in a person's blood decrease to a critical level, they become increasingly vulnerable to illness. Healthcare workers rely on a CD4 count when making decisions about when HIV-positive patients should begin antiretroviral therapy.

The majority of patients in the developing world do not currently have access to CD4 testing because it is expensive, and relies on sophisticated laboratory testing and specially trained operators. Where testing facilities exist, it is often too difficult for people in rural areas to access them and it can take weeks to obtain results.

Having completed the first phase of trials, the prototype test developed by the Burnet Institute scientists will undergo further validation and clinical studies to ensure the assay offers reliable and reproducible results.

Related Links:

Burnet Institute



Gold Member
TORCH Panel Rapid Test
Rapid TORCH Panel Test
Automated Blood Typing System
IH-500 NEXT
New
Histamine ELISA
Histamine ELISA
New
Newborn Screening Test
NeoMass AAAC 3.0

Latest Microbiology News

Unique Blood Biomarker Shown to Effectively Monitor Sepsis Treatment

High-Accuracy Bedside Test to Diagnose Periprosthetic Joint Infection in Five Minutes

Innovative Diagnostic Approach for Bacterial Infections to Enable Faster and Effective Treatment