Factors Associated with Sample Rejection for CD4+/CD8+ T Cell Count Analyses at the Kenyatta National Hospital Comprehensive Care Center Laboratory, Kenya

Moherai Wilfred Felix, J. Nyagol, W. Mwanda
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Abstract

Background: The appropriate time to initiate antiretroviral therapy (ART) in HIV/AIDS patients is determined by measurement of CD4+/CD8+ T cell count. The CD4/CD8+ T cell count is also useful, together with viral load, in monitoring disease progression and effectiveness treatment regimens. Several factors may contribute to sample rejection during the CD4+/CD8+ T cells count, resulting in negative effects on patient management. Objective: Eva-luate the causes for CD4+CD8+ T cell count sample rejection at the Kenyatta National Hospital Comprehensive Care Center Laboratory. Method: A retrospective cross-sectional study was conducted between 2018 and 2020. Data was obtained from the “rejected samples” for Partec R FlowCyp flow cytometry file. Designed data collection sheet was used for data capture. A total of 3972 samples were submitted for CD4+/CD8+ T cell count during the study period. Causes for sample rejection were numbered 1 to 12, each representing a reason for sample rejection. Number 1 was sub-categorized into clotted, hemolyzed, short-draw and lipemic. Data was analyzed using excel, and presented using tables, graphs and pie charts. Approval to conduct the study was obtained from KNH/UoN ERC. Results: In the study period, 81/3972 (2.0%) samples were rejected. Samples submitted more than 48 hours after collection were mostly rejected. Other factors rate for CD4/CD8+ T cell count was relatively low, and multiple factors con-tributed to rejection. However, improved quality assurance will enable more benefit to patients who seek this test in the laboratory.
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肯尼亚肯雅塔国家医院综合护理中心实验室CD4+/CD8+ T细胞计数分析中与样本排斥相关的因素
背景:HIV/AIDS患者开始抗逆转录病毒治疗(ART)的合适时间是通过测量CD4+/CD8+ T细胞计数来确定的。CD4/CD8+ T细胞计数与病毒载量一起在监测疾病进展和有效治疗方案方面也很有用。在CD4+/CD8+ T细胞计数期间,有几个因素可能导致样本排斥,从而对患者管理产生负面影响。目的:评价肯雅塔国家医院综合护理中心实验室CD4+CD8+ T细胞计数样本排斥反应的原因。方法:2018 - 2020年进行回顾性横断面研究。数据来自“拒绝样本”,用于Partec R FlowCyp流式细胞术文件。采用设计好的数据采集表进行数据采集。在研究期间,共提交了3972份样本进行CD4+/CD8+ T细胞计数。样本拒绝的原因编号为1到12,每个原因代表一个样本拒绝的原因。1分凝血型,溶血型,短血型和血脂型。数据使用excel进行分析,并使用表格、图形和饼状图进行展示。该研究已获得KNH/ un ERC的批准。结果:在研究期间,有81/3972(2.0%)份样本被拒绝。收集后超过48小时提交的样品大多被拒绝。其他因素导致CD4/CD8+ T细胞计数率相对较低,多种因素导致排斥反应。然而,改进的质量保证将使在实验室寻求这种测试的患者受益更多。
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