Frequency of Red Blood Cell Alloimmunization in Patients with Sickle Cell Disease in Palestine.

Q3 Medicine Advances in Hematology Pub Date : 2018-06-06 eCollection Date: 2018-01-01 DOI:10.1155/2018/5356245
Fekri Samarah, Mahmoud A Srour, Dirgham Yaseen, Kamal Dumaidi
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引用次数: 17

Abstract

Background: Transfusion of red blood cells (RBC) is an essential therapeutic tool in sickle cell disease (SCD). Repeated RBC transfusions can cause alloimmunization which causes difficulty in cross-matching and finding compatible blood for transfusions. This study aimed to investigate the frequency of RBC alloimmunization and related risk factors among Palestinian SCD patients.

Materials and methods: A multicenter cross-sectional study on 116 previously transfused SCD patients from three centers in West Bank, Palestine. Demographic, medical data and history of transfusion were recorded. Blood samples were collected from transfused consenting SCD patients. Gel card method was used for antibody screening and identification. In all patients, autocontrol and direct antiglobulin (DAT) test were performed using polyspecific (anti-IgG + C3d) anti-human globulin (AHG) gel cards for the detection of autoantibodies.

Results: Of the SCD patients, 62 (53.4%) patients were HbSS and 54 (46.6%) patients were sickle β-thalassemia (S/β-thal). There were 53 (45.7%) females and 63 (54.3%) males. Mean age was 18.8 years (range 3-53 years). The frequency of RBC alloimmunization among SCD patients was 7.76%, with anti-K showing the highest frequency (33.3%) followed by anti-E (22.2%), anti-D (11.1%), anti-C (11.1%), and anti-c (11.1%). All reported IgG alloantibodies were directed against antigens in the Rh (66.7%) and Kell (33.3%) systems. Older ages of patients, increased number of blood units transfused, and splenectomy were the commonest risk factors for alloimmunization in our study.

Conclusions: RBC alloimmunization rate among Palestinian SCD patients is low compared to neighboring countries and countries all over the world but still warrants more attention. Phenotyping of donors/recipients' RBC for Rh antigens and K1 (partial phenotype matching) before their first transfusion may reduce the incidence of alloimmunization.

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巴勒斯坦镰状细胞病患者红细胞同种免疫的频率。
背景:红细胞(RBC)输注是镰状细胞病(SCD)的重要治疗手段。重复输注红细胞可引起同种异体免疫,导致交叉配型和寻找相容的输血血液困难。本研究旨在探讨巴勒斯坦SCD患者的红细胞同种异体免疫频率及其相关危险因素。材料和方法:对来自巴勒斯坦西岸三个中心的116例既往输血的SCD患者进行多中心横断面研究。记录人口统计、医疗资料和输血史。血液样本采集自同意输血的SCD患者。采用凝胶卡法进行抗体筛选和鉴定。所有患者均采用多特异性(抗igg + C3d)抗人球蛋白(AHG)凝胶卡进行自体对照和直接抗球蛋白(DAT)试验,检测自身抗体。结果:SCD患者中,HbSS 62例(53.4%),镰状β-地中海贫血54例(46.6%)。其中女性53例(45.7%),男性63例(54.3%)。平均年龄18.8岁(范围3-53岁)。SCD患者的红细胞异体免疫频率为7.76%,其中抗k抗体的频率最高(33.3%),其次是抗e抗体(22.2%)、抗d抗体(11.1%)、抗c抗体(11.1%)和抗c抗体(11.1%)。所有报告的IgG同种抗体均针对Rh(66.7%)和Kell(33.3%)系统中的抗原。在我们的研究中,患者年龄较大、输血单位数增加和脾切除术是同种异体免疫最常见的危险因素。结论:巴勒斯坦SCD患者的红细胞异体免疫率与周边国家和世界各国相比较低,但仍值得重视。在首次输血前对供者/受者的红细胞进行Rh抗原和K1(部分表型匹配)的表型分型可以降低同种异体免疫的发生率。
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来源期刊
Advances in Hematology
Advances in Hematology Medicine-Hematology
CiteScore
3.30
自引率
0.00%
发文量
10
审稿时长
15 weeks
期刊最新文献
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