期刊文献+

CA19-9测定在4个免疫检测系统的差异及互认能力的评估 被引量:9

Comparison and harmonization assessment of mutual among four different immunoassay systems in CA19-9 test
原文传递
导出
摘要 目的 研究4个免疫检测系统对CA19-9检测的差异和一致性,探讨实现CA19-9检测结果互认的基础.方法 检测系统比对研究.汇集整理CA19-9室间质量评价活动批号的数据(卫生部200811 ~ 201215,浙江省080309 ~ 120211);搜集120份不同CA19-9浓度的新鲜血样本;搜集2010年9月至2012年3月不同检测系统非肿瘤体检人群实测CA19-9数据.选择4个稳定的检测系统Abbott Architect i2000、Roche E170、Beckman Dxi800和Siemens CentaurXP作为研究对象,统计分析在卫生部和浙江省室间质评(冻干粉和液体血清)中的组间差异;参照CLSI EP9-A2进行120份新鲜血样本的比对分析;计算各检测系统实测CA19-9的95%置信区间并分析.采用散点图、加权回归方程进行统计比较.结果 室间质评与新鲜血比对出现颠倒的结果.室间质评均表现出检测系统组间较大的偏倚,斜率bw在1.340到4.683之间,相关系数r较好;新鲜血比对中r不理想,但斜率bw接近于1.新鲜血比对中在推荐浓度27 U/ml时,检测系统两两间偏移分别为Abbott-Roche(-6.41%),Beckman-Roche(-5.07%),Siemens-Roche(13.15%),Beckman-Abbott(2.46%),Siemens-Abbott(22.52%),Siemens-Beckman(39.66%).部分检测系统间实测95%置信区间差异有统计学意义.结论 在研究检测系统差异时,在较低浓度CA19-9的结果在4个检测系统间具有互认的基础,但在高浓度时,检测系统间的差异明显增大,风险较高,尚无法实现互认. Objective To investigate the differences and harmonization of immunoassay systems in detecting CA19-9 and to assess the possibility of mutual recognition in different laboratories. Methods Data were collected and analyzed from External Quality Assessments (EQA) of NCCL( Lots :200811-201215) and ZJCCL(Lots:080309-120211) . 120 fresh serum with different concentrations of CA19-9 were collected. The CA19-9 results of healthy people were also collected from September 2010 to March 2012. Four kinds of stable immunoassay systems were involved in our research, including Abbott Architect i2000, Beckman UniCel DxI 800, Roche E170 and Siemens ADVIA Centaur XP. The differences among four system groups were calculated with the EQA data. The fresh serum comparisons were also performed following the guideline of CLSI EP9-A2 The 95% confidence interval of each immunoassay system was calculated . Comparisons were made by scatter diagrams and weighted regression. Results Both EQA of NCCL and ZJCCL showed better correlation coefficients and larger bias (bW ranged from 1. 340 to 4. 683 ) than in fresh serum comparisons. Although the correlation coefficients were all unsatisfactory, the bw were all close to 1 in fresh serum comparisons. When the recommended serum concentration of 27 U/ml was used, the biases were Abbott-Roche - 6. 41% , Beckman-Roche - 5.07% , Siemens-Roche 13.15%, Beckman-Abbott 2.46%, Siemens-Abbott 22. 52% and Siemens-Beckman 39.66%, respectively. Differences of 95% confidence intervals were statistically significant among parts of the immunoassay systems. Conclusions Only in the lower concentration can CA19-9 results be mutual recognized among four different immunoassay systems, there will be larger differences and risks in the higher concentration.
出处 《中华检验医学杂志》 CAS CSCD 北大核心 2013年第9期812-817,共6页 Chinese Journal of Laboratory Medicine
关键词 CA19-9抗原 肿瘤标记 生物学 质量控制 CA19-9 antigen Tumor markers, biological Quality control
  • 相关文献

参考文献12

  • 1中华人民共和国卫生部.卫办医发(2006)32号.卫生部办公厅关于医疗机构间医学检验、医学影像检査互认有关问题的通知.北京:卫生部,2006.
  • 2浙江省卫生厅.浙卫发(2006)157号.《关于贯彻落实医疗机构间医学检验医学影像检查互认有关问题的通知》.浙江:卫生厅,2006.
  • 3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
  • 4Fleisher M, Dnistrian AM,Sturgeon CM, et al. Practiceguidelines and recommendations for use of tumor markers in theclinic. Tumor Markers : Physiology, Pathobiology, Technology,and Clinical Applications, 2002 :33-64.
  • 5Sturgeon CM, Hoflman BR, Chan DW, et al. National Academyof Clinical Biochemistry Laboratomy Medicine Practice Guidelinesfor use of tumor markers in clinical practice : quality requirements. Clin Chen, 2008,54:el-el0.
  • 6Miller WG, Myers GL, Rej R. Why commutability matters. ClinChem, 2006, 52:553-554.
  • 7王薇,钟堃,白玉,何法霖,张妍,王治国.北京市常规化学检验结果互认项目在全国室间质评中的结果分析[J].中华检验医学杂志,2012,35(1):62-66. 被引量:9
  • 8National Committee for Clinical Laboratory Standards. Methodcomparison and bias estimation using patient samples. EP9-A2.Wayne, PA:NCCLS; 1995.
  • 9中华人民共和国医政司.全国临床检验操作规程.3版.南京:东南大学出版社,2006:690-705.
  • 10曾洁,赵海舰,张传宝,申子瑜,陈文祥.19项临床生化检验项目的分析前变异和个体内生物学变异[J].中华检验医学杂志,2010,33(8):776-781. 被引量:35

二级参考文献38

  • 1Callum GF.Biological Variation:from principles to practice.Washington DC:AACC press,2001.
  • 2Fraser CG.Analytical goals in clinical biochemistry.Prog Clin Pathol,1981,8:101-122.
  • 3Harris EK,Kanofsky P,Shakarji G,et al.Biological and analytic components of variation in long-term studies of serum constituents in normal subjects.Clin Chem,1970,16:1022-1027.
  • 4Fraser CG,Cummings ST,Wilkinson SP,et al.Biological variability of 26 clinical chemistry analytes in elderly people.Clin Chem,1989,35:783-786.
  • 5Young DS,Keffler SM.Effects of Preanalytical variables on clinical laboratory tests.3rd ed.Washington DC:AACC press,2007.
  • 6Carmen R.Desirable specifications for total error,imprecision,and bias,derived from intra-and inter-individual biologic variation[DB/OL].Madison:Westgard QC,1999 (2008)[2009-11-30].http://www.westgard.com/biodatabasel.htm.
  • 7Tanner M,Kent N,Smith B,et al.Stability of common biochemical analytes in serum gel tubes subjected to various storage temperatures and times pre-centrifugation.Ann Clin Biochem,2008,45:375-379.
  • 8Lippi G,Salvagno GL,Montagnana M,et al.Influence of shortterm venous stasis on clinical chemistry testing.Clin Chem Lab Med,2005,43:869 -875.
  • 9Rynning M,Wentzel-Larsen T,Bolann BJ.A model for an uncertainty budget for preanalytical variables in clinical chemistry analyses.Clin Chem,2007,53:1343-1348.
  • 10Fuentes-Arderiu X,Acebes-Frieyro G,Gavaso-Navarro L,et al.Pre-metrological (pre-analytical) variation of some biochemical quantities.Clin Chem Lab Med,1999,37:987-989.

共引文献111

同被引文献34

引证文献9

二级引证文献51

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