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Beckman-Coulter LX20生化检测系统与HITACHI7080自建系统肾功能测定的对比研究 被引量:4

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摘要 由于检验项目所涉及的仪器、试剂、校准品、质控品、检验程序等的不同,不同的生化检测系统测定的结果会有偏差。为实现生化测定的溯源性和可比性,我们依据美国临床实验室标准化委员会(NCCLS)EP9-A文件,对2个生化检测系统进行尿素(Urea)、肌肝(Cr)及尿酸(UA)3项指标的测定,并进行结果比对和偏差评估。
出处 《检验医学》 CAS 北大核心 2011年第1期69-70,共2页 Laboratory Medicine
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参考文献3

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共引文献84

同被引文献29

  • 1陈文祥.临床检验量值溯源与参考系统[J].中华检验医学杂志,2006,29(1):17-19. 被引量:41
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  • 4National Committee for Clinical Laboratory Standards. EP9-A Method comparison and bias estimation using patient samples ap- proved guideline[S]. Wayne PA: NCCLS, 1995.
  • 5Clinical and Laboratory Standards Institute. C54-A Verification of comparability of patient results within one health care system: Approved guideline[S]. Wayne PA:CLSI,2008.
  • 6National Committee for Clinical Laboratory Standards. EP9-A Method comparison and bias estimation using patient samples ap- proved guideline[S]. Wayne PA: NCCLS, 1995.
  • 7Intemational Organization for Standardization. IDT in vitro diagnostic medical devices -measurement of quantities in biological samples - metrological traceability of values assigned to calibrators and control materials. Geneva: ISO,2003 : 3-23.
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  • 9National Committee for clinical Laboratory Standards.EP9-A2 Method Comparison and bias estimation using patient samples. Approved Guideline[S].Wayne PA:NCCLS,2002.
  • 10缪丽韶,温冬梅,张秀明.患者新鲜混合血清作为临时校准液校正非配套检测系统[J].检验医学与临床,2009,6(21):1825-1826. 被引量:2

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