Comprehensive evaluation of the internal and external quality control to redefine analytical quality goals

被引:15
作者
Varela, Beatriz [1 ]
Pacheco, Gonzalo [1 ]
机构
[1] Qual Assurance & Qual Control Dept, Lab Anal Clin, Montevideo, Uruguay
关键词
total quality management; quality control; bias; laboratory proficiency testing/methods; clinical chemistry test; SIGMA-METRICS; ANALYTICAL PERFORMANCE; CLINICAL-CHEMISTRY; PRECISION; ERRORS;
D O I
10.11613/BM.2018.020710
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Introduction: The aim of this work is to design a selection algorithm for total allowable error (TEa) source using a graphic tool that, by integrating internal (IQC) and external (EQC) quality control performances, enables the laboratory to evaluate which TEa source better fits the test analytical performance. Materials and methods: Two analytical performance indicators (bias and Sigma metrics) were estimated for 23 biochemistry tests during 2016. Bias was estimated on the EQC, and Sigma metrics was calculated through the results obtained in the IQC. The Sigma metrics was charted as a function of the bias (TEa%). Following the proposed algorithm (considering the hierarchy in the Milan 2014 consensus), the TEa was evaluated depending on two areas. One area in the chart was defined as the objective area in which the used TEa is the appropriate one for the analytical performance of the test under evaluation. For any test located outside this area, a performance re-evaluation was required using another source of TEa. Results: In 19 out of 23 evaluated tests, the resulting analytical performance allowed for the selection of biologic variability as TEa source. In the four remaining cases, TEa sources of lesser hierarchy were selected. Conclusion: The graphic tool designed together with the proposed algorithm enabled the laboratory to standardize the selection procedure of the most appropriate TEa for the test analytical performance.
引用
收藏
页数:11
相关论文
共 21 条
[1]  
Afrifa Justice, 2015, Niger Med J, V56, P54, DOI 10.4103/0300-1652.149172
[2]  
[Anonymous], 2012, Medical laboratories-requirements for quality and competence
[3]   Adding value to laboratory medicine: a professional responsibility [J].
Beastall, Graham H. .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2013, 51 (01) :221-227
[4]   Errors in a stat laboratory: Types and frequencies 10 years later [J].
Carraro, Paolo ;
Plebani, Mario .
CLINICAL CHEMISTRY, 2007, 53 (07) :1338-1342
[5]  
Forsman RW, 1996, CLIN CHEM, V42, P813
[6]  
Fraser CG, 2001, BIOL VARIATION PRINC, P29
[7]   ASVCP guidelines: allowable total error guidelines for biochemistry [J].
Harr, Kendal E. ;
Flatland, Bente ;
Nabity, Mary ;
Freeman, Kathleen P. .
VETERINARY CLINICAL PATHOLOGY, 2013, 42 (04) :424-436
[8]   Sigma metrics used to assess analytical quality of clinical chemistry assays: importance of the allowable total error (TEa) target [J].
Hens, Koen ;
Berth, Mario ;
Armbruster, Dave ;
Westgard, Sten .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2014, 52 (07) :973-980
[9]  
International Organization for Standardization, 2015, 135282015 ISO
[10]   Errors in clinical laboratories or errors in laboratory medicine? [J].
Plebani, Mario .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2006, 44 (06) :750-759