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Alloimmunization Rates and Associated Factors in Transfusion-Dependent Patients: a Regional Study from Saudi Arabia
Clinical Laboratory
|January 16, 2026
Summary
Alloimmunization affects 10.2% of transfusion-dependent patients in Aseer, linked to Rh-D positivity and high transfusion volume. Strategies like extended phenotyping can reduce this risk.
Area of Science:
- Hematology
- Immunology
- Transfusion Medicine
Background:
- Blood transfusions are vital but carry risks, including alloimmunization from repeated exposure.
- Alloimmunization, the development of antibodies against foreign red blood cells, poses a significant challenge in managing transfusion-dependent patients.
- Understanding the prevalence and risk factors for alloimmunization is crucial for patient safety and effective transfusion strategies.
Purpose of the Study:
- To determine the prevalence of alloimmunization in transfusion-dependent patients in the Aseer province.
- To identify key risk factors associated with alloimmunization in this patient cohort.
- To inform the development of targeted interventions to mitigate alloimmunization risks.
Main Methods:
- Retrospective analysis of medical records for 149 transfusion-dependent patients.
- Data collected included patient demographics, diagnosis, blood group, Rh phenotype, and transfusion history.
- Prevalence of alloantibodies and association with clinical factors were assessed.
Main Results:
- The overall prevalence of alloimmunization was 10.2% (15 out of 149 patients).
- Alloimmunization was more common in patients with blood group O and Rh-D positive status.
- Significant risk factors included older age, Rh-D positivity, and receiving over 15 transfusion units annually.
Conclusions:
- Transfusion-dependent patients, especially those with Rh-D positivity and high transfusion burden, face an elevated risk of alloimmunization.
- Implementing extended red cell phenotyping and matched transfusion protocols can help minimize alloimmunization.
- Optimized transfusion policies are essential to reduce alloimmunization complications in this population.
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