Metrological traceability as a tool to standardize measurements in Laboratory Medicine. Basics for the correct application of the concept of metrological traceability in laboratory measurements are the univocal definition of the measurand and of an unbroken metrological traceability chain, the demonstration of the commutability of calibration materials, the correction of the measurement bias and the estimate of combined uncertainty at each level of the metrological chain. In vitro diagnostics (IVD) manufacturers should ensure traceability of their analytical systems to recognized higher-order references (materials and/or methods) and estimate the combined uncertainty of calibrators. End-users should check the IVD traceability through the verification that control materials of analytical systems are in the manufacturer’s declared validation range and through the organization of EQAS that meet metrological criteria. Separately, they should also estimate the contribution to measurement uncertainty by random effects. Main unsolved issues are the lack of full information about sources of traceability and uncertainty of commercial calibrators, the lack of objective analytical specifications and the need to properly define and use ‘traceable’ reference intervals.

Riferibilità metrologica come strumento per la standardizzazione delle misure in Medicina di Laboratorio = Metrological traceability as a tool to standardize measurements in Laboratory Medicine / F. Braga, M. Panteghini. - In: BIOCHIMICA CLINICA. - ISSN 0393-0564. - 39:6(2015 Dec), pp. 551-558.

Riferibilità metrologica come strumento per la standardizzazione delle misure in Medicina di Laboratorio = Metrological traceability as a tool to standardize measurements in Laboratory Medicine

F. Braga;M. Panteghini
Primo
2015

Abstract

Metrological traceability as a tool to standardize measurements in Laboratory Medicine. Basics for the correct application of the concept of metrological traceability in laboratory measurements are the univocal definition of the measurand and of an unbroken metrological traceability chain, the demonstration of the commutability of calibration materials, the correction of the measurement bias and the estimate of combined uncertainty at each level of the metrological chain. In vitro diagnostics (IVD) manufacturers should ensure traceability of their analytical systems to recognized higher-order references (materials and/or methods) and estimate the combined uncertainty of calibrators. End-users should check the IVD traceability through the verification that control materials of analytical systems are in the manufacturer’s declared validation range and through the organization of EQAS that meet metrological criteria. Separately, they should also estimate the contribution to measurement uncertainty by random effects. Main unsolved issues are the lack of full information about sources of traceability and uncertainty of commercial calibrators, the lack of objective analytical specifications and the need to properly define and use ‘traceable’ reference intervals.
Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
dic-2015
Centro Interdipartimentale sulla Riferibilità Metrologica in Medicina di Laboratorio - CIRME
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/349634
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