期刊文献+

ISO 15189:2012与临床检验定量检测方法确认和性能验证 被引量:53

下载PDF
导出
摘要 ISO 15189:2012对技术要求的检验过程分别单独列出了对检验程序确认和验证、测量不确定度的要求,并将其改为强制要求。本文参考相关文件,结合我国实际情况,扼要介绍方法性能评价关键指标的基本概念及不同检测系统的实施方案。对配套系统,实验室应进行验证实验,至少包括精密度、正确度和可报告范围;对非配套系统,实验室应进行确认研究,至少包括正确度、精密度、可报告范围及生物参考区间等。以期为临床实验室更合理地评价和应用检测方法提供参考。
出处 《临床检验杂志》 CAS CSCD 北大核心 2013年第12期881-884,共4页 Chinese Journal of Clinical Laboratory Science
  • 相关文献

参考文献31

  • 1ISO 15189. Medical laboratories-Requirements for quality and com- petence [ S ]. International Organization for Standardization, 2012. ISO 15189.
  • 2Medical laboratories-Particular requirements for quality and competence [ S ]. International Organization for Standardization, 2007.
  • 3卫医发[2006]73号.医疗结构临床实验室管理办法[s].中华人民共和国卫生部,2006.
  • 4国家质量监督检验检疫总局.JJF1001-2011通用计量术语及定义[S],2011.
  • 5GB/T22576-2008.医学实验室质量和能力的专用要求[s].中国国家标准化管理委员会,2010.
  • 6WS/T4202013.f临床实验室对商品定量试剂盒分析性能的验证[s].中华人民共和国国家卫生和计划生育委员会,2013.
  • 7CNAS-CL38.医学实验室质量和能力认可准则在临床化学检验领域的应用说明[S].中国合格评定国家认可中心,2012.
  • 8CLSI EP15-A2. User verification of performance for precision and trueness; approved guideline- second edition [ S ]. CLSI, 2005.
  • 9王治国.临床检验方法确认与性能验证[M].北京:人民卫生出版社,2008:123-125.
  • 10Knudsen CS, Nexo E, Hcjskov CS, et al. Analytical validation of the Roche 25-0H vitamin D total assay[ J. Clin Chem Lab Med, 2012, 50( 11 ) : 1965-1968.

二级参考文献39

  • 1罗浔阳,张劼,孙兵,王菁菁,徐志晔.2台日立7600生化分析仪6种血清酶测定结果可比性评价[J].临床检验杂志,2007,25(4):297-297. 被引量:23
  • 2中国合格评定国家认可委员会.CNAS-GL02:能力验证结果的统计处理和能力评价指南[S].2006.
  • 3CLSI. Evaluation of the Linearity of Quantitative Measurement Procedures : A Statistical Approach ; Approved Guideline [ S ]. EP6-A, 2003,23(16) :1-46.
  • 4U. S. Department of Health and Human Services. 42CFR Part 493 : medicare, medicaid and CLIA programs; Laboratory requirements relating to quality systems and certain personnel qualifications; Final rule[ J ]. Federal Register,2003,68:3640-3714.
  • 5Siekmann L, Bonora R, Burtis CA, et al. IFCC primary reference procedures for the measurement of catalytic activity concentrations of enzymes at 37~C. Part 7. Certification of four reference materials for the determination of enzymatic activity of -y-glutamyltransferase, lac- tate dehydrogenase, alanine aminotransferase and creatine kinase ac- cording to IFCC procedures at 37~C [ J~. Clin Chem Lab Med ,2002, 40(7 ) :739-745.
  • 6ISO Guide 35. Reference materials-general and statistical principles for certification[ S ]. ISO, 2006.
  • 7ISO 18153. In vitro diagnostic medical devices measurement of quan- tities in biological samples metrological traceability of values for cata- lytic concentration of enzymes assigned to calibrators and control ma- terials[ S]. JCTLM, 2003.
  • 8ISO 15189. Medical laboratories-particular requirements for quality and competence[S]. ISO, 2003.
  • 9EP9-A2. Method comparison and bias estimation using patient sam- ples ; approved guideline-second edition [ S ]. NCCLS ,2002.
  • 10Bland JM, Altman DG. Measuring agreement in method comparison studies[J]. Statistical Methods in Medical Research, 1999, 8 (2) : 135-160.

共引文献65

同被引文献303

引证文献53

二级引证文献207

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部