Detecting Long-term Drift in Reagent Lots

被引:28
作者
Liu, Jiakai [1 ]
Tan, Chin Hon [1 ]
Loh, Tze Ping [2 ]
Badrick, Tony [3 ]
机构
[1] Natl Univ Singapore, Dept Ind & Syst Engn, Singapore 117548, Singapore
[2] Natl Univ Singapore Hosp, Dept Lab Med, Singapore 117548, Singapore
[3] Bond Univ, Fac Hlth Sci & Med, Southport, Qld 4229, Australia
关键词
QUALITY-CONTROL; CUSUM;
D O I
10.1373/clinchem.2015.242511
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
BACKGROUND: Between-reagent lot verification is a routine laboratory exercise in which a set of samples is tested in parallel with an existing reagent lot and a candidate reagent lot (before the candidate lot is committed to test patient samples). The exercise aims to verify and maintain consistency in the analytical performance of a test. We examined the limitations of a routine between-reagent lot verification procedure in detecting long-term analytical drift and looked for a more sensitive alternative. METHOD: Via numerical simulations, we examined the statistical power of the current regression-based (weighted Deming regression) procedure for between-reagent lot verification in detecting proportional bias and constant bias. An alternative procedure applying the Student t-test to separately examine cumulative regression slopes and intercepts across multiple reagent lots was proposed and evaluated by numerical simulations. RESULTS: The regression-based procedure had poor statistical power in detecting proportional bias and constant bias when small numbers of samples were used in each between-reagent lot verification exercise. Furthermore, the method failed to detect long-term drifts in analytical performance. The proposed approach based on the Student t-test can detect long-term (cumulative) drifts in regression slopes and intercepts. This method detected a mild downward drift in the serum sodium assay in our hospital that was missed by routine between-reagent lot verification. CONCLUSIONS: The proposed method objectively and systematically detects long-term proportional and constant bias separately. However, the statistical power of this procedure remains unsatisfactory when used with small sample sizes. Sharing of information between laboratories may provide sufficient statistical power to detect clinically important analytical shifts. (C) 2015 American Association for Clinical Chemistry
引用
收藏
页码:1292 / 1298
页数:7
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