沙特阿拉伯镰状细胞病患儿红细胞同种免疫的患病率

A. Baothman, Badriah Al-Asmari, Mohammed Almohammad, Mohammed M Aljuaid, W. Jastaniah
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摘要

目的:镰状细胞病(SCD)是一种常见的遗传性血红蛋白疾病。镰状细胞病患者的主要治疗方法之一是输血。输血后红细胞抗原的异体免疫仍然是SCD患者的主要风险。本研究的目的是确定本中心儿童SCD患者红细胞同种异体免疫的发生率、性质和危险因素,并将我们的结果与KSA、区域和一些国际国家发表的报告进行比较。方法:采用回顾性研究设计,回顾2008-2019年吉达阿卜杜勒阿齐兹国王医疗城(KAMC-J) SCD患者的记录,使用免疫血液学技术分析血液样本进行同种异体免疫。记录人口统计学特征和输血史。数据分析采用SPSS ver软件。26. 数据汇总为频率分布,采用卡方检验检验各亚组间同种异体抗体频率差异的显著性。结果:在所有检查的镰状细胞患者中(n=112)。21例(17.4%)患者检出同种异体抗体,其中15例(71.4%)患者多为单一异体抗体,分别为抗k(23.7%)、抗e(19.0%)和抗s(9.5%)。其他6例(28.6%)存在多种同种异体抗体,其中以抗c和抗k合用(9.5%)和抗c和抗e合用(9.5%)最多。同种异体抗体在年住院次数> 5次、换血次数、年龄> 3岁和输血次数较多的患者中显著升高(p值< 0.05)。建议:红细胞同种异体免疫的后果非常显著,因此,强烈建议将红细胞抗原扩展到包括ABO、RH (D、C、C、E、E)、K、Fya、Fyb、Jka和Jkb抗原,以确保更好的输血做法并避免输血相关并发症。与其他国家相比,我们频繁输血后的同种异体免疫率相对较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence of Red Blood Cell Alloimmunization Among Pediatric Patients with Sickle Cell Disease in Saudi Arabia
Purpose: Sickle cell disease (SCD) is a common global hereditary hemoglobin disorder. One of the main treatments of sickle cell patients is the requirement of blood transfusions. Post transfusion alloimmunization of red blood cell antigens continue to be a major risk for SCD patients. The study objective is to determine the rate, nature, and risk factors of red cell alloimmunization among pediatric SCD patients in our center and compare our results to published reports from the KSA, regional and some international countries. Methodology: A retrospective study drsign was adopted with record review of SCD patients at King AbdulAziz Medical City-Jeddah (KAMC-J) between 2008-2019 where blood samples were analyzed for alloimmunization using immunohematological techniques. Demographic characteristics and transfusion history were recorded. Data analysis was conducted by SPSS ver. 26. Data are summarized as frequency distribution and chi square test was used to check significance of the difference in the frequency of alloantibodies among subgroups.   Findings: Out of all examined sickle cell patients (n=112). Alloantibodies were detected in 21 patients (17.4%), and these were mostly single in 15 patients (71.4%) as anti-K (23.7%), anti-E (19.0%), and anti-S (9.5%). The other six patients (28.6%) had multiple alloantibodies, especially the combination of anti-C and anti-K (9.5%) and the combination of anti-C and anti-E (9.5%). Alloantibodies were significantly higher in patients who had been admitted to the hospital > 5 times annually, those who had an exchange blood transfusion, age groups > 3 years, and for those who received a larger number of blood units (p-value < 0.05). Recommendations: The consequences of red blood cell alloimmunization are highly significant and, therefore, extended RBC antigens to include ABO, RH (D, C, c, E, e), K, Fya, Fyb, Jka and Jkb antigens in the screening panel for donors and recipients is highly recommended to ensure better transfusion practices and avoid transfusion related complications. Our rate of alloimmunization post frequent blood transfusion is considered relatively low compared to other nations.
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