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The change in load capacity between the control specimens and other groups are found within the acceptable single laboratory coefficient of variation precision 1 s % of 14.4%.
The method's interassay laboratory coefficient of variation is ∼4.7%.
Using the standards developed in the National Glycohemoglobin Standardization Program, this method of percentage of HbA1c assessment was calibrated to the reference range of 4.3 6.0% (23 42 mmol/mol) and a laboratory coefficient of variation range 1.4 1.9% (21).
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In our laboratory, coefficients of variation (CV) for PCT were found to be <10 % at 0.28 and 10.8 µg/L.
Short-term in vivo precision using this device was similar in children to that observed in adults in our laboratory; coefficients of variation for between-day measurements were 1.8, 0.6, and 3.2% for BUA, SOS, and SI, respectively.
Within-batch laboratory coefficients of variation were 13.6% or less.
Laboratory coefficients of variation were less than 5% for all individual estrogens and estrogen metabolites measured and less than 3% for estrone, estradiol, and estriol.
Intra-laboratory coefficient of variance (CV) for the one-stage assay was typically below 10% (Table 1).
The intra-laboratory coefficient of variation (CV) for assessment of sperm concentration was found to be less than 8.5percentt.
For this study, the assay used had a detection limit of 4 pmol/L; the inter-laboratory coefficient of variation (CV) was 20% at 18 pmol/l, 10% at 50 pmol/l, and <6% for plasma NT-proSST concentrations above 100 pmol/L (highest calibrator concentration used was 2500 pmol/L).
In our laboratories, coefficients of variation for procalcitonin were <4 % at 2 concentrations during the study period.
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