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The maximum mean difference between two instruments was as high as 0.33 mmol/l (range 0.21 0.50 mmol/l).
The maximum difference between two instruments was 0.09 mmol/L (95 % CI 0.02 mmol/L) for systemic samples and 0.33 mmol/L (95 % CI ± 0.01 mmol/L; median Δ 0.29 mmol/L; 0.21 0.50 mmol/L) for post filter samples.
In the Schwarzer et al. study, the maximum mean difference between two instruments was 0.33 mmol/l (median 0.29 mmol/l, range 0.21 0.50 mmol/l) for postfilter iCa values despite internal quality controls within the 14%% variation of combined imprecision and bias according to national regulation.
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The relative bias between two instruments is not known exactly, but must be estimated and corrected for.
When both portable and bench top blood samples are each taken directly from the finger the mean difference between [lactate] measured by the portable and bench top analyzers was small across the full range of lactate values as depicted in figure 2. While the mean difference between the two instruments was near zero, differences between the instruments had a large variability (SD=1.45 mM/l).
The correlation between the two instruments was strong (r = 0.89, P < 0.0001).
The correlation between the two instruments was high (r2 = 0.87-0.94) concerning total internal-external rotation.
Finally, the relationship between the two instruments was assessed by correlation analysis.
For implicit time, the mean local difference between the two instruments was 0.01 Z-score.
For severe levels of micturition frequency (4 and 5), difference in utilities between the two instruments was not statistically significant.
Finally, as expected, the relationship between the two instruments was significantly negative, lending support to their convergent validity.
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