Abstract

IntroductionBy quantifying the measurement uncertainty (MU), both the laboratory and the physician can have an objective estimate of the results’ quality. There is significant flexibility on how to determine the MU in laboratory medicine and different approaches have been proposed by Nordtest, Eurolab and Cofrac to obtain the data and apply them in formulas. The purpose of this study is to compare three different top-down approaches for the estimation of the MU and to suggest which of these approaches could be the most suitable choice for routine use in clinical laboratories.Materials and methodsImprecision and bias of the methods were considered as components of the MU. The bias was obtained from certified reference calibrators (CRC), proficiency tests (PT), and inter-laboratory internal quality control scheme (IQCS) programs. The bias uncertainty, the combined and the expanded uncertainty were estimated using the Nordtest, Eurolab and Cofrac approaches.ResultsUsing different approaches, the expanded uncertainty estimates ranged from 18.9-40.4%, 18.2-22.8%, 9.3-20.9%, and 7.1-18.6% for cancer antigen (CA) 19-9, testosterone, alkaline phosphatase (ALP), and creatinine, respectively. Permissible values for MU and total error ranged from 16.0-46.1%, 13.1-21.6%, 10.7-26.2%, and 7.5-17.3%, respectively.ConclusionThe bias was highest using PT, followed by CRC and IQCS data, which were similar. The Cofrac approach showed the highest uncertainties, followed by Eurolab and Nordtest. However, the Eurolab approach requires additional measurements to obtain uncertainty data. In summary, the Nordtest approach using IQCS data was therefore found to be the most practical formula.

Highlights

  • By quantifying the measurement uncertainty (MU), both the laboratory and the physician can have an objective estimate of the results’ quality

  • Using different approaches, the expanded uncertainty estimates ranged from 18.9-40.4%, 18.2-22.8%, 9.3-20.9%, and 7.1-18.6% for cancer antigen (CA) 19-9, testosterone, alkaline phosphatase (ALP), and creatinine, respectively

  • Permissible values for MU and total error ranged from 16.0-46.1%, 13.1-21.6%, 10.7-26.2%, and 7.5-17.3%, respectively

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Summary

Introduction

By quantifying the measurement uncertainty (MU), both the laboratory and the physician can have an objective estimate of the results’ quality. By quantifying the variation in the results, both the clinical laboratory performing the measurements and the physician receiving the results can have an objective estimate of the quality of the results [2]. Clinical laboratories looking forward the accreditation under the ISO 15189 standard, shall determine measurement uncertainty for each measurement procedure, and define and regularly check their performance requirements concerning uncertainty [4]. Particular approach for determining measurement uncertainty (MU) [5] It states, “The laboratory shall determine measurement uncertainty for each measurement procedure...”, allowing significant flexibility on how to determine it [4,6]

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