Frequency of Red Blood Cells Alloimmunization in Thalassemia Patients at King Abdulaziz University Hospital in Jeddah, Saudi Arabia

Salwa A. Alnajjar, T. Tayeb, Abdulrahman S. Alboog, Tarek Elgemmezi, S. Hindawi
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引用次数: 4

Abstract

The aim of the study is to assess the alloimmunization rate to red blood cell in thalassemia patients at King Abdulaziz University Hospital. Thalassemia is the most common genetic disorder worldwide that represents a major public health problem and requires long life blood transfusion to the patients as the main treatment. Alloimmunization to the transfused red blood cell can cause hemolytic transfusion reactions and significantly complicate transfusion therapy. Screening and identification of alloantibodies and transfusion of extended phenotyped blood can minimize these risks. A retrospective study was conducted on 134 thalassemia patients at King Abdulaziz University Hospital in Jeddah. Patients’ samples were subjected to red cell typing, antibody screening and identifi cation of red blood cell antibodies. Alloimmunization in thalassemia patients was 20.15%; antibodies were mainly to the Rh and Kell blood group systems, the highest rate was for anti-E (32.4%) followed by anti-K (21.6%). Alloimmunization rate was the highest in the age group from > 10 – 20 years (40.7%). Red cell alloimmunization is a frequent event among thalassemia patient. A national protocol for screening and identifying of the red cell alloantibodies and transfusion of phenotype blood is required for proper management of these patients.
沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学医院地中海贫血患者红细胞同种免疫频率
本研究的目的是评估阿卜杜勒阿齐兹国王大学医院地中海贫血患者的红细胞异体免疫率。地中海贫血是世界上最常见的遗传性疾病,是一个重大的公共卫生问题,需要向患者长期输血作为主要治疗方法。输注红细胞的同种异体免疫可引起溶血性输血反应,使输血治疗明显复杂化。筛选和鉴定同种异体抗体和输血扩展表现型血液可以最大限度地减少这些风险。对吉达阿卜杜勒阿齐兹国王大学医院134名地中海贫血患者进行了回顾性研究。对患者标本进行红细胞分型、抗体筛选和红细胞抗体鉴定。地中海贫血患者同种异体免疫率为20.15%;抗体主要针对Rh和Kell血型系统,其中抗e型抗体阳性率最高(32.4%),其次是抗k型抗体(21.6%)。同种异体免疫率以10 ~ 20岁年龄组最高(40.7%)。红细胞异体免疫是地中海贫血患者中常见的事件。为了对这些患者进行适当的管理,需要制定一项筛查和鉴定红细胞同种抗体和输血的国家方案。
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