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Analytical Imprecision and Reference Change Values for Longitudinal Monitoring of NCD-Related Biochemical Analytes
Siti Nurwani Ahmad Ridzuan1, Muhammad Nursyazwan Zamre1, Fadzlyasraf Shaari2
1Special Protein Unit, Specialized Diagnostic Centre, Institute for Medical Research, National Institutes of Health, Jalan Pahang, Kuala Lumpur 50588, Malaysia.
Abstract:
Background: Internal quality control (IQC) data offers continuous insight into analytical performance under routine conditions. This study evaluated IQC practices and long-term analytical imprecision (CVa) across primary healthcare laboratories to derive analyte-specific reference change values (RCVs) for non-communicable disease (NCD) monitoring. Methods: A 22-month retrospective analysis of IQC data was conducted across 29 primary healthcare laboratories using 32 analytical units (Beckman Coulter AU480) in Malaysian primary healthcare. Six analytes were assessed: glucose, creatinine, total cholesterol, triglycerides, HDL cholesterol, and ALT. CVa was estimated using median and 90th percentile (P90) coefficients of variation across two concentration levels. RCVs were calculated at 95% probability (Z = 1.96) by integrating observed CVa with within-subject biological variation (CVi) from EFLM databases. Results: IQC testing was highly standardized (median: 20 measurements/month). Long-term data showed stable, concentration-dependent imprecision. Median CVa was lowest for glucose and lipids (1.7-1.9%) but higher for ALT (3.79%) and creatinine (3.52%) at Level 1. Derived RCV ranged from 14% (glucose) to 55.1% (triglycerides), with CVi being the dominant contributor to RCV magnitude for most analytes. Conclusions: Long-term routine IQC data provide an analytically realistic foundation for deriving RCV in primary healthcare by reflecting real-world performance. Applying these RCV supports evidence-based interpretation of serial results, enhancing NCD monitoring by distinguishing true physiological change from analytical and biological noise.
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