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Identifying D-positive donors using a second automated testing platform
1MD (corresponding author), Executive Medical Director, Donor and Transplantation Services.
Immunohematology
|December 12, 2013
Summary
Evaluating a second automated blood testing platform for D antigen detection revealed a very low yield in preventing alloimmunization in women under 50. This finding suggests current methods may suffice for most blood donors.
Area of Science:
- Transfusion Medicine
- Immunohaematology
- Blood Donor Screening
Background:
- Variability in D antigen expression necessitates reliable methods for classifying blood donors with variant RHD alleles.
- Current automated testing may be insufficient for accurate D antigen typing, potentially leading to alloimmunization risks.
Purpose of the Study:
- To evaluate the efficacy of the Immucor Gamma Galileo automated platform in confirming D- results from the Beckman Coulter PK7300 system.
- To estimate the number of alloimmunization cases preventable in women under 50 by implementing dual automated testing.
Main Methods:
- Comparison of D antigen testing results between PK7300 and Galileo automated platforms for first-time blood donors.
- Discordant samples were further analyzed using serologic tube methods, RHD genotyping (BLOODchip), and sequencing.
- Estimation of alloimmunization prevention based on transfusion data and known alloimmunization rates.
Main Results:
- Of 15,441 first-time donors with concordant D- results, five showed D+ on Galileo. One was a false positive; four had positive serologic tests and were C+.
- Further RHD genotyping identified weak D types 67, 9, and two novel variants among the four discordant donors.
- The addition of Galileo testing was estimated to prevent approximately one case of alloimmunization every 5-6 years in women under 50.
Conclusions:
- Adding a second automated serologic testing platform (Galileo) shows a very low yield in preventing alloimmunization in the target population.
- Current D antigen testing strategies appear adequate for most blood donors, with limited benefit from an additional automated platform for this specific outcome.
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