Analysis of Molecular Blood Group Determination in Patients at the University Clinical Hospital Mostar over a 2.5-year Period
Keywords:
ABO blood group; RhD variants; RHD genotyping; molecular typing; transfusion medicine; alloimmunization; weak D; partial D; DEL variantAbstract
Background: The study aimed to analyze the frequency of ABO and RhD genotypes, including RHD variant alleles, and to evaluate the clinical value of molecular genotyping in comparison with standard serological findings.
Methods: A total of 162 patients were included, all of whom underwent comprehensive serological and molecular typing of the ABO and RhD systems using PCR-based methods to identify weak, partial, and DEL RhD variants as well as other rare alleles, with correlation to transfusion history and clinical indications.
Main findings: The results demonstrated a predominance of blood group A and O, while blood groups B and AB were less frequent, with the majority of patients being RhD positive. A significant number of weak and partial RhD variants were identified, particularly among transfusion recipients and patients with a positive Coombs test. Molecular genotyping enabled clarification of serological discrepancies and precise determination of the Rh phenotype, ensuring a more rational use of RhD-negative blood units.
Principal conclusion: These findings confirm the importance of molecular analysis of the ABO and RhD systems in optimizing transfusion practice, reducing the risk of alloimmunization, and supporting an individualized approach to patient care.