2021年埃塞俄比亚西北贡达尔大学综合专科医院人类免疫缺陷病毒感染成人遗传性球细胞增多症的程度GC,横断面研究设计

Samuel Sahile Kebede, A. Yalew, T. Yesuf, Getachew Mesfin Bambo, Tadesse Duguma, Berhanu Woldu
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引用次数: 1

摘要

背景:遗传性球形红细胞增多症是一种溶血性贫血,其特点是临床异质性,遗传上确定的红细胞膜异常导致溶血危象。HS在80%的患者中为常染色体显性遗传,其余20%为隐性基因或散发性遗传。目的:本研究的主要目的是确定2021年3月至4月在埃塞俄比亚西北部贡达尔大学综合专科医院感染人类免疫缺陷病毒的成年人中免疫遗传性球形红细胞增多症的程度。方法:采用系统随机抽样的方法,于2021年3月至4月在贡达尔大学综合专科医院对358名人类免疫缺陷病毒感染者进行机构横断面研究。社会人口统计数据采用结构化预测问卷收集。每位受试者抽取静脉血5ml,经Unicel DHX 800血液学分析仪分析,并进行血膜检查和抗人球蛋白试验,排除免疫性溶血性贫血。数据输入Epidata 4.6版本,使用STATA 14版本进行分析。描述性统计是用图表和图形来计算和绘制的。结果:遗传性球形红细胞增多症的患病率为2 / 358。发生遗传性球形红细胞增多症的两个个体均为女性,年龄在22至35岁之间。总患病率为91(25.42%)。在这些贫血研究人群中,分别有3人(3.29%)、28人(30.77%)和60人(65.93%)患有重度、中度和轻度贫血。结论和建议:遗传性球形红细胞增多症是人类免疫缺陷病毒感染成人中较少见的疾病。在这些患者中,通过使用测试算法,在家族水平上早期发现和治疗是必要的。
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The Magnitude of Hereditary Spherocytosis Among Human Immunodeficiency Virus-Infected Adults Attending University of Gondar Comprehensive Specialized Hospital Northwest Ethiopia 2021 GC, Cross-Sectional Study Design
Background: Hereditary spherocytosis is a type of hemolytic anemia characterized by a clinically heterogeneous, genetically defined red blood cell membrane abnormality that results in hemolytic crisis. The inheritance of HS is autosomal dominant in 80% of affected individuals and recessive genes or sporadic type in the remaining 20%. Objective: The main aim of this study was to determine the magnitude of immune hereditary spherocytosis among human immunodeficiency virus-infected adults at the University of Gondar comprehensive specialized hospital in northwest Ethiopia from March to April 2021. Methods: An institution-based cross-sectional study was conducted on 358 human immunodeficiency virus-infected adults selected by systematic random sampling at the University of Gondar comprehensive specialized hospital from March to April 2021. Data for socio-demographic data were collected by structured pretested questionnaire. Five ml of venous blood was drawn from each participant and analyzed by Unicel DHX 800 hematology analyzer, and blood film examination and antihuman globulin test were performed to exclude immune hemolytic anemia. Data was entered into Epidata version 4.6 and analyzed by STATA version 14. Descriptive statistics were computed and drawn in charts and graphs. Results: The prevalence of hereditary spherocytosis was 2 of 358 participants. Both individuals who developed hereditary spherocytosis were females and in the age group of 22 to 35. The overall prevalence of anemia was 91 (25.42%). Of those anemic study population 3 (3.29%), 28 (30.77%), and 60 (65.93%), respectively, had severe, moderate, and mild anemia. Conclusion and Recommendation: Hereditary spherocytosis is a less frequent condition in human immunodeficiency virus-infected adults. In these patients, early detection and treatment are necessary at the familial level by using a test algorithm.
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