학술논문

Risk factors for red blood cell alloimmunization in the Recipient Epidemiology and Donor Evaluation Study (REDS‐III) database
Document Type
article
Source
British Journal of Haematology. 181(5)
Subject
Biomedical and Clinical Sciences
Cardiovascular Medicine and Haematology
Prevention
Rare Diseases
Hematology
Clinical Research
Adolescent
Adult
Aged
Aged
80 and over
Anemia
Sickle Cell
Arthritis
Rheumatoid
Blood Donors
Blood Group Antigens
Child
Child
Preschool
Databases
Factual
Erythrocyte Transfusion
Female
Humans
Immunization
Infant
Isoantibodies
Lupus Erythematosus
Systemic
Male
Middle Aged
Myelodysplastic Syndromes
Risk Factors
Transfusion Reaction
red blood cells
alloimmunization
antibodies
transfusion
NHLBI Recipient Epidemiology and Donor Evaluation Study-III
Cardiorespiratory Medicine and Haematology
Immunology
Cardiovascular medicine and haematology
Language
Abstract
Despite the significance of red blood cell (RBC) alloimmunization, the lack of standardized registries in the US has prevented the completion of large studies. Data from 3·5 years of the Recipient Epidemiology and Donor Evaluation Study-III (REDS-III) recipient database, containing information from 12 hospitals, were studied. A RBC alloantibody responder had an antibody identified at any point during the study, and a non-responder had a negative antibody screen at least 15 days post-RBC transfusion. Demographics, blood type, ICD9/10 codes, and other potential correlates were evaluated. Of 319 177 (2·07%) screened patients, 6597 had a total of 8892 clinically significant RBC alloantibodies identified, with 75% being in the Rh or Kell families. Alloimmunization was more common in females (2·38%) than males (1·68%), and in RhD negative (2·82%) than RhD positive (1·94%) patients. Age, sex, RhD status and race were associated with being a responder, and certain diagnoses (including sickle cell disease or trait, systemic lupus erythematosus, rheumatoid arthritis and myelodysplastic syndrome) were more common among responders than non-responders. Data collected in this multi-centre recipient database provide the largest RBC alloimmunized patient cohort studied in the US, with previously known demographic and disease associations of responder status confirmed, and new associations identified.