Abstract

Analytical validation of automated erythrocyte sedimentation rate (ESR) analyzers is necessary prior to their implementation into routine practice. Our aim was toperform the analytical validation of the modified Westergren method applied on the CUBE 30 touch analyzer (Diesse, Siena, Italy). Validation included determination of within-run and between-run precision following the Clinical and Laboratory Standards Institute EP15-A3 protocol, comparison with the reference Westergren method, sample stability assessment at both room temperature and 4°C, after 4, 8 and24-h storage, and checking the extent of hemolysis and lipemia interference. Coefficients of variation (CVs) for within-run precision were 5.2% for the normal and 2.6% for the abnormal range, while between-run CVs were 9.4 and 2.2%, respectively. Comparison with the Westergren method (n=191) yielded Spearman's correlation coefficient of 0.93, noconstant nor proportional difference [y=0.4 (95% CI:-1.7-1.0)+1.06 (95% CI: 1.00-1.14)x] and a non-significant mean absolute bias of-2.6mm (95% CI:-5.3-0.2). Lower comparability was evidenced with increasing ESR values, with both constant and proportional differences for ESR values between 40 and 80mm, and above 80mm. Sample stability was not compromised up to 8-h storage both at room temperature (p=0.054) and 4°C (p=0.421). Hemolysis did not affect ESR measurement up to 1.0g/L of free hemoglobin (p=0.089), while lipemia index above 5.0g/L affects the ESR result (p=0.004). This study proved that CUBE 30 touch provides reliable ESR measurement and satisfactory comparability with the reference Westergren methods, with minor variation related to methodological differences.

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