期刊文献+

Sysmex XT-1800i,XS-800i和Mythic-22检测结果可比性研究 被引量:1

Comparative Study on Result of Blood Cells with Hematological Analyzers of Sysmex XT-1800i,Sysmex XS-800i and Mythic-22
下载PDF
导出
摘要 目的 探讨日本Sysmex XT-1800i,Sysmex XS-800i和瑞士Mythic-22全自动血细胞分析仪对同一份标本测定结果的可比性.方法 以Sysmex XT-1800i为目标检测系统(对比方法),并对其进行精密度、准确度评价.以Sysmex XS-800i和Mythic-22为实验检测系统(实验方法).以门诊和部分住院患者新鲜全血进行血常规检测,对WBC及分类、RBC,HGB,HCT和PLT计算相关系数和回归方程,以美国临床实验室修正法规(CLIA'88)规定的室间质量评价允许误差的1/2为标准,判断不同检测系统WBC,RBC,HGB,HCT和PLT的可比性.结果 Sysmex XT-1800i血细胞分析仪WBC,RBC,HGB,HCT和PLT精密度在允许范围内,质控项目中除Sysmex XS-800i RBC高值外,其余项目在不同检测系统上的测定结果均具有可比性.非质控项目白细胞分类只有嗜碱性粒细胞相关性差,分别为r=0.349和r=0.427.结论 对该室内不同血细胞检测系统定期进行测定结果的可比性分析,以及时发现系统误差,并进行校准,为临床和患者提供准确的可比性报告. Objective To investigate comparability of the results of the same blood with hematological analyzers of Sysmex XT-1800i,Sysmex XS-800i and Mythic-22. Methods To assess the accuracy,the intra and inter-assay precision of Sysmex XT-1800i. Compared Sysmex XS-800i, Mythic-22 (laboratory method) to sysmex XT-1800i (comparison method ), items including WBC,RBC,HGB,HCT and PLT,elass of WBC and to obtain the correlation coefficient and the linear equation. E- valuate the system bias of WBC,RBC,HGB,HCT and PLT between laboratory method and comparison method according to the half of CLLA'88. Results The precision were allowed of Sysmex XT-1800i. Quality control items were comparative,except the high RBC of Sysmex XS-8.00i. The result of Bas were not satisfied (r=0. 349,r=0. 427). Conclusion It was necessary to examine different hematology with method comparison in time to improve the accurate report for clinic and patient.
作者 高峰 张宏杰
出处 《现代检验医学杂志》 CAS 2011年第2期34-36,共3页 Journal of Modern Laboratory Medicine
关键词 血细胞分析仪 对比研究 hematological analyzers comparative study
  • 相关文献

参考文献5

二级参考文献6

  • 1National Committee for Clinical Laboratory Standards. Reference leukocyte differential count (proportional) and evaluation of instrument methods: approved standard. NCCLS Document H20-A [S].NCCLS, Wayne (USA), 1992.
  • 2International Organization for Standardization.General Requirements for the Competence of Testing and Calibration Laboratories.ISO/IEC 17025,International Organization for Standardization,Geneva,1999.
  • 3The National Committee for Clinical Laboratory Standards.Method Comparison and Bias Estimation Using Patient Samples.Approved Guideline,Second Edition,EP9-A2,2002.
  • 4Siekmann L,Bonora R,Burtis CA,et al.IFCC primary reference procedures for the measurement of catalytic activity concentrations of enzymes at 37 degrees C.International Federation of Clinical Chemistry and Laboratory Medicine.Part 7.Certification of four reference materials for the determination of enzymatic activity of gamma-glutamyltransferase,lactate dehydrogenase,alanine aminotransferase and creatine kinase accord.Clin Chem Lab Med,2002,40:739-745.
  • 5郭健,王清涛,童清,杨振华.血清酶测定标准化的实验研究[J].中华检验医学杂志,2002,25(3):147-149. 被引量:42
  • 6王清涛,童清,郭健.血清酶测定结果可溯源性研究[J].中华检验医学杂志,2003,26(12):761-763. 被引量:23

共引文献139

同被引文献9

引证文献1

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