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Clinical Chemistry 43: 886-892, 1997;
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(Clinical Chemistry. 1997;43:886-892.)
© 1997 American Association for Clinical Chemistry, Inc.

Articles

Thoughts on quality-control systems: a laboratorian's perspective

George S. Cembrowskia

a Address for correspondence: GSC Consulting, 4913 Bruce Ave., Edina, MN 55424. Fax 612-915-1061, e-mail cembr001{at}gold.tc.umn.edu

State-of-the-art prospective quality-control systems entail the use of medically relevant, analyte-specific quality control limits. With analyte-specific limits broader than those generally used in the clinical laboratory, there will be fewer false rejections, fewer unnecessary reanalyses, and shorter delays in run reporting. If the analyte-specific limits are narrower than those used in the laboratory, more errors will be detected, but the user is at risk of identifying errors over which s/he and the manufacturer have little control. The use of various patient data quality-control algorithms is described. Conservatism is stressed in adopting manufacturers' guidelines for surrogate, nondestructive quality-control testing. A simple, optimized approach is suggested for the systematic retrospective review of proficiency data. Finally, an approach is presented for converting from older, previously accepted quality control procedures to more efficient analyte-specific quality control.




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Copyright © 1997 by the American Association for Clinical Chemistry.