...
首页> 外文期刊>Annals of laboratory medicine. >Analysis of Factors Influencing the Generation of Unqualified Clinical Samples and Measures to Prevent this Generation
【24h】

Analysis of Factors Influencing the Generation of Unqualified Clinical Samples and Measures to Prevent this Generation

机译:影响不合格临床样品生成的因素分析及防止这种生成的措施

获取原文
           

摘要

Background: We investigated the influence of pre-analytical factors on the results of clinical tests and thereby analyzed approaches to improve quality management in clinical laboratories. Methods: Unqualified clinical samples were selected from all the samples received at our clinical laboratory. The data were collected for 2009 and 2010, i.e., the years before and after the establishment of the laboratory quality management system. The rate and causes of generation of unqualified samples were analyzed, and measures to improve the laboratory practices were studied and implemented. Results: A total of 1,051 unqualified samples were identified from among the 553,158 samples (the overall incidence rate of unqualified samples was 0.19%). The number of unqualified samples substantially varied according to the nature of the sample, and clinical samples collected for routine blood tests or coagulation tests were the predominant unqualified samples. The main causes of generation of unqualified samples were insufficient sample volumes and improper methods of mixing the samples. The rate of generation of unqualified samples decreased significantly after the implementation of improvement measures (0.26% in 2009 vs. 0.13% in 2010, P Conclusions: The number of unqualified samples decreased significantly after the establishment of the laboratory quality management system, which promoted active communication among and training of the clinical staff to reduce the occurrence of pre-analytical errors. Comprehensive control of pre-analytical factors is an important approach in improving the clinical laboratory practices.
机译:背景:我们调查了分析前因素对临床测试结果的影响,从而分析了改善临床实验室质量管理的方法。方法:从我们临床实验室收到的所有样本中选择不合格的临床样本。收集了2009年和2010年的数据,即实验室质量管理体系建立前后的年份。分析了不合格样品的产生率和原因,并研究和实施了改善实验室操作的措施。结果:553,158个样本中共鉴定了1,051个不合格样本(不合格样本的总发生率为0.19%)。不合格样品的数量根据样品的性质而有很大不同,以常规血液检查或凝血试验收集的临床样品为主要不合格样品。产生不合格样品的主要原因是样品量不足和混合样品方法不当。实施改进措施后,不合格样品的产生率显着下降(2009年为0.26%,2010年为0.13%,P)结论:建立实验室质量管理体系后,不合格样品的数量明显减少,促进了实验室质量管理体系的建立。临床人员之间的沟通和培训,以减少分析前错误的发生,全面控制分析前因素是改善临床实验室操作的重要途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号