Ca. Parvin et Am. Gronowski, EFFECT OF ANALYTICAL RUN-LENGTH ON QUALITY-CONTROL (QC) PERFORMANCE AND THE QC PLANNING PROCESS, Clinical chemistry, 43(11), 1997, pp. 2149-2154
The performance measure traditionally used in the quality-control (QC)
planning process is the probability of rejecting an analytical run wh
en an out-of-control error condition exists. A shortcoming of this per
formance measure is that it doesn't allow comparison of QC strategies
that define analytical runs differently. Accommodating different analy
tical run definitions is straightforward if QC performance is measured
in terms of the average number of patient samples to error detection,
or the average number of patient samples containing an analytical err
or that exceeds total allowable error. By using these performance meas
ures to investigate the impact of different analytical run definitions
on QC performance demonstrates that during routine QC monitoring, the
length of the interval between QC tests can have a major influence on
the expected number of unacceptable results produced during the exist
ence of an out-of-control error condition.