The EuBIVAS: Within- and Between-Subject Biological Variation Data for Electrolytes, Lipids, Urea, Uric Acid, Total Protein, Total Bilirubin, Direct Bilirubin, and Glucose

Author:

Aarsand Aasne K123,Díaz-Garzón Jorge4,Fernandez-Calle Pilar34,Guerra Elena5,Locatelli Massimo5,Bartlett William A36,Sandberg Sverre123,Røraas Thomas23,Ceriotti Ferruccio7,Sølvik Una Ørvim28,Sverresdotter Sylte Marit1,Coşkun Abdurrahman39,Serteser Mustafa9,Unsal Ibrahim9,Tosato Francesca10,Plebani Mario10,Jonker Niels311,Barla Gerhard11,Carobene Anna35

Affiliation:

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

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

3. Working Group on Biological Variation, European Federation of Clinical Chemistry and Laboratory Medicine, Milan, Italy

4. Hospital Universitario La Paz, Madrid, Spain, and Quality Analytical Commission of Spanish Society of Clinical Chemistry (SEQC), Barcelona, Spain

5. Servizio di Medicina di Laboratorio, Ospedale San Raffaele, Milan, Italy

6. Blood Sciences, Ninewells Hospital & Medical School, Dundee, UK

7. Central Laboratory, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy

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

9. Acibadem University, School of Medicine, Atasehir, Istanbul, Turkey

10. Department of Laboratory Medicine University Hospital, Padua, Italy

11. Certe, Wilhelmina Ziekenhuis Assen, Assen, the Netherlands

Abstract

Abstract BACKGROUND The European Federation of Clinical Chemistry and Laboratory Medicine European Biological Variation Study (EuBIVAS) has been established to deliver rigorously determined data describing biological variation (BV) of clinically important measurands. Here, EuBIVAS-based BV estimates of serum electrolytes, lipids, urea, uric acid, total protein, total bilirubin, direct bilirubin, and glucose, as well as their associated analytical performance specifications (APSs), are presented. METHOD Samples were drawn from 91 healthy individuals (38 male, 53 female; age range, 21–69 years) for 10 consecutive weeks at 6 European laboratories. Samples were stored at −80 °C before duplicate analysis of all samples on an ADVIA 2400 (Siemens Healthineers). Outlier and homogeneity analyses were performed, followed by CV-ANOVA on trend-corrected data, when relevant, to determine BV estimates with CIs. RESULTS The within-subject BV (CVI) estimates of all measurands, except for urea and LDL cholesterol, were lower than estimates available in an online BV database, with differences being most pronounced for HDL cholesterol, glucose, and direct bilirubin. Significant differences in CVI for men and women/women <50 years of age were evident for uric acid, triglycerides, and urea. The CVA obtained for sodium and magnesium exceeded the EuBIVAS-based APS for imprecision. CONCLUSIONS The EuBIVAS, which is fully compliant with the recently published Biological Variation Data Critical Appraisal Checklist, has produced well-characterized, high-quality BV estimates utilizing a stringent experimental protocol. These new reference data deliver revised and more exacting APS and reference change values for commonly used clinically important measurands, thus having direct relevance to diagnostics manufacturers, service providers, clinical users, and ultimately patients.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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