Valid analytical performance specifications for combined analytical bias and imprecision for the use of common reference intervals

Author:

Hyltoft Petersen Per12,Lund Flemming1,Fraser Callum G3,Sandberg Sverre245,Sölétormos György6

Affiliation:

1. Department of Clinical Biochemistry, Nordsjællands Hospital, University of Copenhagen, Hillerød, Denmark

2. Norwegian Quality Improvement of Laboratory Examinations (NOKLUS), Haraldsplass Deaconess Hospital, Bergen, Norway

3. Centre for Research into Cancer Prevention and Screening, University of Dundee, Dundee, Scotland

4. Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway

5. Laboratory of Clinical Biochemistry, Haukeland University Hospital, Bergen, Norway

6. Department of Research, Nordsjællands Hospital, University of Copenhagen, Hillerød, Denmark

Abstract

Background Many clinical decisions are based on comparison of patient results with reference intervals. Therefore, an estimation of the analytical performance specifications for the quality that would be required to allow sharing common reference intervals is needed. The International Federation of Clinical Chemistry (IFCC) recommended a minimum of 120 reference individuals to establish reference intervals. This number implies a certain level of quality, which could then be used for defining analytical performance specifications as the maximum combination of analytical bias and imprecision required for sharing common reference intervals, the aim of this investigation. Methods Two methods were investigated for defining the maximum combination of analytical bias and imprecision that would give the same quality of common reference intervals as the IFCC recommendation. Method 1 is based on a formula for the combination of analytical bias and imprecision and Method 2 is based on the Microsoft Excel formula NORMINV including the fractional probability of reference individuals outside each limit and the Gaussian variables of mean and standard deviation. The combinations of normalized bias and imprecision are illustrated for both methods. The formulae are identical for Gaussian and log-Gaussian distributions. Results Method 2 gives the correct results with a constant percentage of 4.4% for all combinations of bias and imprecision. Conclusion The Microsoft Excel formula NORMINV is useful for the estimation of analytical performance specifications for both Gaussian and log-Gaussian distributions of reference intervals.

Publisher

SAGE Publications

Subject

Clinical Biochemistry,General Medicine

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Bias in Laboratory Medicine: The Dark Side of the Moon;Annals of Laboratory Medicine;2023-09-04

2. Reference intervals: past, present, and future;Critical Reviews in Clinical Laboratory Sciences;2023-04-10

3. Evaluation of Groundwater Using an Integrated Approach of Entropy Weight and Stochastic Simulation: A Case Study in East Region of Beijing;International Journal of Environmental Research and Public Health;2021-07-20

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