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Impact of a common CV evaluation scheme on overall laboratory performance: 8-year experience of a large national proficiency testing program in Japan

  • Kiyoshi Ichihara and Tadashi Kawai
Published/Copyright: September 21, 2011

Abstract

In proficiency testing (PT), it is difficult to set rational criteria for determining target values and allowable limits. In Japan, the largest national PT program has for the past 8years used an evaluation scheme based on a “common coefficient of variation” (cCV) to overcome this difficulty. The cCV, the average within-method variation, is derived by one-way analysis of variance from data of peer groups after excluding those with large variations. A unit interval used for grading participants is obtained by multiplying the cCV by the peer-group mean which is computed using an iterative method featuring repeated removal of a large portion of the tails of the distribution and reinflation of the standard deviation (SD) to compensate for the trimming. The evaluation scheme gives a relatively better grade to those participants in peer groups with small CVs, compared to use of individual peer-group CVs. The scheme has expedited the transition to more reproducible methods, resulting in a notable overall improvement in laboratory performance. The cCV evaluation scheme is uniformly applicable to any analyte measured quantitatively. The iterative method, an integral part of the scheme, effectively precludes bias in the evaluation.


Corresponding author: Kiyoshi Ichihara, MD, PhD, Department of Clinical Laboratory Sciences, Faculty of Health Sciences, Yamaguchi University School of Medicine, Minami-Kogushi 1-1-1, Ube, 755-8505 Japan Phone/Fax: +81-836-22-2884,

References

1 Ross JW. A theoretical basis for clinically relevant proficiency testing evaluation limits. Arch Pathol Lab Med 1988; 112: 421–34. Search in Google Scholar

2 Laessig RH, Ehrmeyer SS, Leinweber JE. Intralaboratory performance requirements necessary to pass proficiency testing: CAP-1990 vs. CLIA-1967 (March 14, 1990) formats compared. Clin Chem 1992; 38: 895–903. 10.1093/clinchem/38.6.895Search in Google Scholar

3 Hamilin W. Proficiency testing as regulatory device: a CAP perspective. Clin Chem 1992; 38: 1234–36. 10.1093/clinchem/38.7.1234Search in Google Scholar

4 Shahangian S. Proficiency testing in laboratory medicine: use and limitations. Arch Pathol Lab Med 1998; 122: 15–30. Search in Google Scholar

5 Tholen DW. Reference values and participant means as targets in proficiency testing. Arch Pathol Lab Med 1993; 117: 885–9. Search in Google Scholar

6 Ichihara K, Kawai T. An iterative method for improved estimation of the mean of peer-group distributions in proficiency testing. Clin Chem Lab Med 2005; 43: 412–21. 10.1515/CCLM.2005.074Search in Google Scholar

7 Kanno T. Improvement of inter-laboratory imprecision in enzyme measurements (in Japanese). Rinsho Byori 2001; 116( Suppl): 16–25. Search in Google Scholar

8 Itoh Y, Ichihara K, Kanno T, Sugawara T, Ohkubo A, Hirabayashi Y, et al. Serum protein standardization project in Japan: evaluation of an IFCC reference material (RPPHS/CRM470) and establishment of reference intervals. J Clin Lab Anal 1997; 11: 39–44. 10.1002/(SICI)1098-2825(1997)11:1<39::AID-JCLA7>3.0.CO;2-FSearch in Google Scholar

9 Itoh Y, Ichihara K. Standardization of immunoassay for CRM470-related proteins in Japan: from evaluating CRM470 to setting reference intervals. Clin Chem Lab Med 2001; 39: 1054–61. 10.1515/CCLM.2001.182Search in Google Scholar

Received: 2004-8-27
Accepted: 2005-1-26
Published Online: 2011-9-21
Published in Print: 2005-4-1

© by Walter de Gruyter Berlin New York

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