Clinical Chemistry AACC Online Job Center
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Clinical Chemistry 38: 1773-1778, 1992;
This Article
Right arrow Full Text (PDF)
Right arrow Submit an electronic Letter to
the Editor about this paper
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sadler, W. A.
Right arrow Articles by Turner, J. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sadler, W. A.
Right arrow Articles by Turner, J. G.

Clinical Chemistry, Vol 38, 1773-1778, Copyright © 1992 by American Association for Clinical Chemistry

Minimum distinguishable difference in concentration: a clinically oriented translation of assay precision summaries

WA Sadler, LM Murray and JG Turner
Department of Nuclear Medicine, Christchurch Hospital, New Zealand.

A trend to market-driven health care in many parts of the world is focusing increasing attention on getting maximum value from available resources. Laboratories are not exempted. Well-informed clinical input has a potentially valuable role in any laboratory rationalization process. However, a communication difficulty exists in the sense that, although laboratory workers, commercial developers, regulatory bodies, etc., are thoroughly conditioned to using assay coefficient of variation as a general performance measure (for excellent reasons), this is not necessarily the most intuitive or informative scale from a clinician's perspective. Here we use routine clinical data from an immunoradiometric assay of thyrotropin to illustrate, first, a general approach to estimation and prediction of reproducibility, and second, an alternative summary that expresses the discriminatory power of an assay. This latter measure, our experience suggests, is more suited to the way clinicians perceive assays and assay results. The overall aim is improved clinician/laboratory communication.


The following articles in journals at HighWire Press have cited this article:


Home page
Clin. Chem.Home page
J. R. Tate, T. Badrick, G. Koumantakis, J. M. Potter, and P. E. Hickman
Reporting of Cardiac Troponin Concentrations
Clin. Chem., November 1, 2002; 48(11): 2077 - 2080.
[Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
E. J. Giltay, C. Popp-Snijders, J. C. van Denderen, D. van Schaardenburg, L. J. G. Gooren, and B. A.C. Dijkmans
Phenylbutazone Can Spuriously Elevate Unextracted Testosterone Assay Results in Patients with Ankylosing Spondylitis
J. Clin. Endocrinol. Metab., December 1, 2000; 85(12): 4923a - 4924.
[Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1992 by the American Association for Clinical Chemistry.