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Environmental Health Criteria 214

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HUMAN EXPOSURE ASSESSMENT<br />

procedures are subject to a variety of analytical inaccuracies or<br />

biases. Fig. 31B shows the effects of a proportional bias in which<br />

the reported values are higher than the expected values. This bias is<br />

called proportional because the amount of bias increases in direct<br />

proportion to the concentration of analyte in the specimen. Fig. 31C<br />

illustrates the effect of a constant bias, in which the reported<br />

values are higher than the expected values by a constant amount, at<br />

all concentrations of analyte. The biases shown in Figs. 31B and 31C<br />

are positive biases, because the reported values are greater than the<br />

expected values. Of course, negative biases may also occur;<br />

furthermore, the reported values may fall along a curve rather than a<br />

straight line. Fig. 31D illustrates combined positive and negative<br />

proportion biases. When combined biases are present, there is<br />

frequently one concentration at which the reported value corresponds<br />

to the expected value. This phenomenon -- that the reported value at<br />

some analyte concentration is the same as the expected value whereas<br />

there is disagreement at all other concentrations -- is commonly<br />

observed and must be considered when interpreting quality control<br />

data. Because of this, it is recommended that reference samples should<br />

cover the range of expected measurement values.<br />

11.5.1.2 Precision<br />

Precision or reliability of an analysis refers to the uniformity<br />

of the results of replicate analyses irrespective of the true<br />

concentration of the analyte. The precision of an analysis may vary<br />

depending on many factors, such as the skill and experience of the<br />

analyst, the purity of the chemicals, the quality of measuring devices<br />

and the time interval between replicate analyses. The precision is<br />

determined by calculating the percentage relative standard deviation<br />

among replicate analyses. In this manner precision can be defined as<br />

the closeness of agreement between independent test results obtained<br />

under prescribed conditions.<br />

The effects of random variation on analyses are illustrated in<br />

Figs. 32A and 32B, which show how laboratory's results may, on the<br />

average, fall along some operational line even though the individual<br />

results are distributed about the line, within certain limits of<br />

variability. Fig. 32A illustrates limits of variability that increases<br />

in proportion to the mean analyte concentration.<br />

http://www.inchem.org/documents/ehc/ehc/ehc<strong>214</strong>.htm<br />

Page 191 of 284<br />

6/1/2007

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