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Letters |
Dept. of Clin. Chem., Inst. of Clin. Pathol. and Medical Res., Westmead Hosp., Westmead NSW 2145, Australia
a Author for correspondence.
To the Editor:
The concept of process capability has been used by the
manufacturing industry to quantify the relation between product
specifications and the measured process performance (1).
Various ratios and indices have been developed to describe this
relation. We have previously reported the application of the simplest
of these, Cp (the capability index or capability ratio), to
the selection of quality-control (QC) algorithms appropriate to the
specification limits and analytical imprecision (2).
Cp is defined as (USL - LSL)/6
, where USL and LSL are
the upper and lower specification limits of an analytical process, and
is the standard deviation of the process.
In contrast to the approach taken by us, the use of medically important
critical systematic error (
SEC) and
References
The following articles in journals at HighWire Press have cited this article:
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W. Gernand How reliable are critical error calculations? Clin. Chem., May 1, 2006; 52(5): 895 - 896. [Full Text] [PDF] |
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