Introduction: Alloimmunization is an immune response to red blood cell antigens, which meet the patient during transfusion therapy, pregnancy, or transplantation. Recipient's immune system recognizes these antigens as foreign and trigger antibody production. Repeated transfusions increase the risk of clinically significant alloantibodies, which may lead to hemolytic transfusion reactions or hemolytic disease of the fetus and newborn. Monitoring transfusion therapy and antibody development is important for patient safety.
Aim of the study: To examine the clinical significance and persistence of alloantibodies in hospizalized patients using two independent hospital information systems: UHC Zagreb and e Delphyn, managed by the Croatian Institute of Transfusion Medicine.
Methods: This retrospective study included all patients in whom RBC alloimmunization was detected during hospitalization at the UHC Zagreb in 2021. Immunohematological testing was performed using the indirect antiglobulin test. For these patients, antbody data were monitored through both systems from the beginning of the system’s operation until end of December 2024, with transfusion treatment and changes in alloantibodies’ persistence. Descriptive statistics were used in analysis.
Results: A total of 284 alloimmunized patients were identified at the UHC, with nearly half also recorded in e-Delphyn. Most of the patients were women (71%) and median age was 68 years. In both systems clinically significant antibodies exceeded 70%, most commonly anti-K, anti-E and anti-D. In the follow-up period, the number of alloantibodies per patient increased, such as number of multiple alloimmunizations. Dynamics of alloantibodies was observed in 9% of patients with nearly equal percentage of appearance and disappearance. Nearly half of patients received transfusion therapy, with a higher intensity observed in the follow-up period.
Conclusion: In alloimmunized population, women and older patients, especially high-risk patients, are predominant. Clinically significant alloantibodies, particularly from Rhesus and Kell systems, are the most prevalent and can cause severe reactions in transfused patients. Monitoring through both systems shows the nature of alloantibodies and highlights the importance of continuous testing and data integration to ensure patient safety.
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