Skip to content
Open access

Analytical Performance Specifications Derived from External Quality Assessment Data: Comparison with Biological Variation-Based Models for Intermediate Precision Assessment.

Aug 2026 · Annals of Laboratory Medicine · 0 citations
Medicine

TL;DR

APSs derived from pooled EQA peer group data provide realistic and technically achievable intermediate precision targets consistent with current AP and thus can complement BV-based specifications.

Abstract

Background Analytical performance specifications (APSs) are essential for quality management in medical laboratories. Considering the discrepancies between laboratory performance and existing guidelines, lack of consideration of concentration-dependent variability, and absence of recommendations for certain parameters, we aimed to define APSs for internal use in biochemistry, hemostasis, and hematology based on external quality assessment (EQA) peer group data and evaluate their suitability for intermediate precision assessment versus biological variation (BV)-based APSs. Methods EQA-based allowable CV (CVallowable) was estimated from pooled CVs derived from EQA peer group results. Allowable bias, expanded measurement uncertainty, and total allowable error were calculated. CVallowable targets were assessed using intermediate precision data from different analytical systems within a laboratory group and compared with BV-based APSs. Concordance between theoretical specifications derived from mathematical models and observed analytical performance (AP) was evaluated using (i) the proportion of internal QC CVs meeting the predefined CVallowable across laboratories and (ii) observed analytical imprecision expressed as a percentage of the allowable imprecision budget. Results APSs were established for 110 biochemical analytes, 23 hemostasis parameters, and 28 hematology parameters across different concentration ranges. EQA-derived APSs agreed with observed intermediate precision for 102 biochemical, 14 hemostasis, and 24 hematology parameters. BV-based APSs showed agreement for only 49 biochemical, two hemostasis, and 11 hematology parameters, while overly restrictive goals or lack of agreement were observed for several analytes. Conclusions APSs derived from pooled EQA peer group data provide realistic and technically achievable intermediate precision targets consistent with current AP and thus can complement BV-based specifications.

Read PDF

Similar papers

Review Oct 2026

A-203 Biological variation reference data; EFLM initiatives and developments to address data quality issues and deliver reliable data.

Biological variation data (BVD), which describes within-subject (CVI) and between-subject (CVG) variability of laboratory measurands, are essential reference data in laboratory medicine. BVD are used to define analytical performance specifications (APS) for imprecision, bias, maximum allowable measurement uncerta...

Kornelia D. Galior, William A. Bartlett, Sverre Sandberg et al. · 0 citations
Oct 2026

Standardized Estimation of Measurement Uncertainty in Clinical Chemistry Using ISO 20914.

BACKGROUND The degree to which one is certain of results for a particular measurement/testing process is expressed as a confidence level within a range. Measurement uncertainty (MU) is a critical parameter in clinical chemistry, reflecting the degree of confidence in laboratory test results and directly influencing dia...

M. I. Ahmad, F. Ahmed, Deepa Rao et al. · 0 citations
Oct 2026

Impact of ISO/TS 20914-based measurement uncertainty on HbA1c diagnostic classification: A real-world comparison of two analytical systems.

OBJECTIVES HbA1c is interpreted using fixed clinical decision limits, but measurement uncertainty (MU) may affect analytical interpretation of results near these thresholds. This study estimated ISO/TS 20914-based MU for two HbA1c analytical systems and evaluated the patient-level impact of including calibration- and t...

A. Gürpınar, Canan Karadağ, M. Katar · 0 citations
Oct 2026

Evaluation of external quality assessment results of 15 clinical laboratory quality indicators in China from 2019 to 2021.

OBJECTIVES This study analyzed external quality assessment (EQA) results for 15 clinical laboratory quality indicators (QIs) in China from 2019 to 2021 to evaluate error-influencing factors, benchmark performance against international standards and inform preliminary quality specifications. METHODS Data for 15 QIs we...

Yuxuan Du, Zhi-Guo Wang, Zhi-Xiang Zhang et al. · 0 citations
Oct 2026

A-404 Determinants of Analytical Performance in Centrifugation–Based Hematocrit: Effects of Calibration and Internal Quality Control Frequency Across Hospital and Primary Point-of-Care Sites

Manual centrifugation–based hematocrit (Hct) remains widely used as point-of-care testing (POCT) in hospital laboratories and subdistrict health promotion hospitals (SDHHs), particularly in decentralized settings. However, evidence is limited on whether quality-related factors influence satisfactory performance w...

Wanvisa Treebuphachatsakul · 0 citations
Oct 2026

A-307 Determining risk-based internal quality control frequency for biochemical testing using Sigma metrics and the QC Constellation tool

Risk-based internal quality control (IQC) has been increasingly adopted in clinical laboratories to enhance analytical quality and patient safety. ISO 15189:2022 recommends designing IQC plans based on risk assessment rather than applying fixed QC frequencies. Sigma metrics combined with the QC Constellation tool...

S. Nguyễn · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.