Using ISO/TS 20914:2019 to calculate the measurement uncertainty of immunosuppressive drugs in a clinical laboratory

Scand J Clin Lab Invest. 2020 Jul;80(4):309-312. doi: 10.1080/00365513.2020.1731849. Epub 2020 Mar 2.

Abstract

According to the standard ISO 15189 clinical routine laboratories shall estimate measurement uncertainty (MU) of patient results of their provided measurands. Up to now there was no accepted description on how to perform. Recently, the ISO technical standard ISO/TS 20914 was published giving a practical guide for uncertainty estimation. The immunosuppressive drugs Everolimus, Ciclosporin, Sirolimus and Tacrolimus have narrow therapeutic windows. Hence, their MU should be considered for deducing clinical decisions. Here, a pathway is presented in detail on how to estimate MU measuring immunosuppressants using a widespread CE certified assay via LC-MS/MS technology. Namely, the expanded measurement uncertainties are from 13% to 27% depending on analyte and concentration. The calculation based on n > 2000 measurements each of four control levels within one year. Lower uncertainties were observed if the material was native pooled blood (13% to 17%, n > 300 measurements, one year).

Keywords: ISO/TS 20914; LC-MS/MS; Measurement uncertainty; ciclosporin; everolimus; immunosuppressants; quality control; sirolimus; tacrolimus.

MeSH terms

  • Chromatography, Liquid
  • Clinical Decision-Making
  • Clinical Laboratory Services / standards
  • Cyclosporine / blood*
  • Drug Dosage Calculations
  • Everolimus / blood*
  • Humans
  • Immunosuppressive Agents / blood*
  • Practice Guidelines as Topic
  • Sirolimus / blood*
  • Tacrolimus / blood*
  • Tandem Mass Spectrometry
  • Uncertainty

Substances

  • Immunosuppressive Agents
  • Cyclosporine
  • Everolimus
  • Sirolimus
  • Tacrolimus