Identification of Pre-analytical Errors in the Laboratory of National Institute of Infectious Diseases, Sri Lanka

P. D. Koggalage, M. P. G. D. Madhubhashini, D. U. Abeysinghe, G. R. D. M. Abeywickrama
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Abstract

Background: Laboratory investigations are the backbone of the diagnosis of diseases. Previous studies have shown that more than 70% of clinical laboratory specimens have to be rejected due to pre-analytical errors.Objective: To determine the sample error rate and identify the causes of sample errors to prevent pre-analytical errors on a laboratory basis.Methods: This is a cross-sectional study. Details were recorded on a data sheet from the received blood samples which were rejected. Sample rejection criteria were described using a formula.Results: The overall sample rejection rate was found to be 71.15%. Incomplete request forms accounted for 54.2% of sample rejections for biochemical samples, while mislabelled blood samples accounted for 35.1% of sample rejections for complete blood counts.Conclusion: According to the study findings, it has shown that relevant healthcare workers should pay more attention to patient investigations relevant to blood samples to provide appropriate patient management with minimal errors in investigation reports.
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斯里兰卡国家传染病研究所实验室分析前误差的鉴定
背景:实验室检查是诊断疾病的基础。以往的研究表明,70%以上的临床实验室标本因分析前误差而被拒收:方法:这是一项横断面研究:这是一项横断面研究。方法:这是一项横断面研究。在数据表上记录了收到的被拒收的血液样本的详细信息。用公式描述了样品拒收标准:结果:总体样本拒收率为 71.15%。不完整的申请表占生化样本拒收率的 54.2%,而贴错标签的血液样本占全血计数样本拒收率的 35.1%:研究结果表明,相关医护人员应更加重视与血液样本相关的患者调查,以便在提供适当的患者管理的同时,尽量减少调查报告中的错误。
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