Comparison of 3 options for choosing control limits in biochemistry testing

© 2017 American Society for Veterinary Clinical Pathology.

Bibliographische Detailangaben
Veröffentlicht in:Veterinary clinical pathology. - 1975. - 46(2017), 1 vom: 15. März, Seite 120-125
1. Verfasser: Manzocchi, Simone (VerfasserIn)
Weitere Verfasser: Furman, Erika, Freeman, Kathleen
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2017
Zugriff auf das übergeordnete Werk:Veterinary clinical pathology
Schlagworte:Comparative Study Journal Article Analytic performance probability of error detection probability of false rejection quality control total allowable error
Beschreibung
Zusammenfassung:© 2017 American Society for Veterinary Clinical Pathology.
BACKGROUND: The purpose of statistical quality control (QC) is to provide peace of mind with regard to the production of results that are suitable for analytically sound clinical interpretation and making reliable decisions about patient diagnosis, monitoring, and prognosis
OBJECTIVES: In this study, we compared 3 options for choosing control limits for biochemistry testing. They focus on the probability of error detection (Ped) and probability of false rejection (Pfr) achievable for a veterinary biochemical analyzer using the following 3 combinations: the quality control material (QCM) manufacturer's acceptable ranges; a standard 12s rule customized for the instrument's observed performance; and candidate rules selected for the instrument's observed performance using a computerized program (EZrules)
METHODS: For assessing customized QC, we used mean, SD, CV, bias, total error, and sigma metrics calculated from 3 months of control measurements on a laboratory biochemical analyzer, for 24 commonly used analytes, on 2 QCM levels
RESULTS: Given the desirable combination of high Ped (> 90%) and low Pfr (≤ 5%), the candidate rules selected by the computerized program-related EZrules provided the best performance combinations
CONCLUSIONS: The present work shows acceptable QC performance basing the QC on customization of the acceptable ranges of results from the achievable performance of an individual instrument. The QC performance is maximized by the application of candidate rules based on customized ranges obtained from a computerized QC tool, providing the ability to achieve the highest Ped and acceptably low Pfr values
Beschreibung:Date Completed 26.09.2017
Date Revised 26.09.2017
published: Print-Electronic
Citation Status MEDLINE
ISSN:1939-165X
DOI:10.1111/vcp.12453