FDA OKs Test to Improve Blood Donor-Recipient Matching

New method uses genetics, computer technology to determine most compatible red blood cells

FRIDAY, May 23, 2014 (HealthDay News) -- The first gene-based test to help determine red blood cell compatibility between a blood donor and a recipient has been approved by the U.S. Food and Drug Administration.

The Immucor PreciseType Human Erythrocyte Antigen (HEA) Molecular BeadChip Test can be used to identify non-ABO red blood cell types, according to the FDA news release. The test is designed to help prevent the development of antibodies to non-ABO antigens by giving patients blood that is better matched to their non-ABO antigens. Experts say that the destruction of red blood cells can be avoided if patients with known non-ABO antigens receive blood that does not contain the same non-ABO antigens.

Current blood testing sometimes fails to detect certain non-ABO antigens. The new test offers a way to detect non-ABO antigens that may otherwise be missed, according to the FDA.

The new test is made by BioArray Solutions Ltd., of Warren, N.J.

Full Article
More Information

Related Stories

No stories found.
logo
www.healthday.com