2015
DOI: 10.1155/2015/610931
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Frequency of Red Cell Alloimmunization and Autoimmunization in Thalassemia Patients: A Report from Eastern India

Abstract: Introduction. Red blood cell (RBC) alloimmunization and autoimmunization remain a major problem in transfusion dependent thalassemic patients. There is a paucity of data on the incidence of RBC alloimmunization and autoimmunization in thalassemic patients from eastern part of India, as pretransfusion antibody screening is not routinely performed. Aims. To assess the incidence of RBC alloimmunization and autoimmunization in transfusion dependent thalassemic patients in eastern India. Materials and Methods. Tota… Show more

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Cited by 31 publications
(22 citation statements)
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“…Although there are some strategies to reduce the risk of RBC alloimmunization, it remains a serious challenge to find compatible RBC units for patients with thalassaemia [17]. The rates of Alloimmunization were reported from 4% to 50% in multitransfused patients and were lower in more homogenous populations [18].…”
Section: Introductionmentioning
confidence: 99%
“…Although there are some strategies to reduce the risk of RBC alloimmunization, it remains a serious challenge to find compatible RBC units for patients with thalassaemia [17]. The rates of Alloimmunization were reported from 4% to 50% in multitransfused patients and were lower in more homogenous populations [18].…”
Section: Introductionmentioning
confidence: 99%
“…However in thalassemia, anti-K comprised major antibodies three of four, that is, 75% followed by anti-E which showed similar results with Roopam et al . [ 20 ] with 80% incidence of anti-K. Higher rate of anti-K alloantibodies could be explained on basis of higher number of Kell positive antigen in donor population of our belt.…”
Section: Discussionmentioning
confidence: 78%
“…The specificity of most alloantibodies detected in this study was against Rh and Kell antigen systems due to their high immunogenicity which is similar to previous reports of alloimmunization. [ 15 20 ]…”
Section: Discussionmentioning
confidence: 99%
“…Patients can be heterozygous for the HbE and β-thalassemia alleles or homozygous for either the HbE or β-thalassemia allele [17]. Because the majority of these patients is transfusion-dependent and prone to alloimmunization [18,19], we detected red cell alloantibodies to blood group antigens in 5.6% of multiply transfused patients with β-thalassemia disease at our hospital in Kolkata [20]. Knowledge of the antigen prevalence allows us to predict the number of red cell units that need to be typed when searching for antigen-negative units.…”
Section: Discussionmentioning
confidence: 96%