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Featured researches published by R. Neill Carey.


Archives of Pathology & Laboratory Medicine | 2005

Performance Characteristics of Several Rules for Self-interpretation of Proficiency Testing Data

R. Neill Carey; George S. Cembrowski; Carl C. Garber; Zohreh Zaki

CONTEXT Proficiency testing (PT) participants can interpret their results to detect errors even when their performance is acceptable according to the limits set by the PT provider. OBJECTIVE To determine which rules for interpreting PT data provide optimal performance for PT with 5 samples per event. DESIGN We used Monte Carlo computer simulation techniques to study the performance of several rules, relating their error detection capabilities to (1) the analytic quality of the method, (2) the probability of failing PT, and (3) the ratio of the peer group SD to the mean intralaboratory SD. Analytic quality is indicated by the ratio of the PT allowable error to the intralaboratory SD. Failure of PT was defined (Clinical Laboratory Improvement Amendments of 1988) as an event when 2 or more results out of 5 exceeded acceptable limits. We investigated rules with limits based on the SD index, the mean SD index, and percentages of allowable error. RESULTS No single rule performs optimally across the range of method quality. CONCLUSIONS We recommend further investigation when PT data cause rejection by any of the following 3 rules: any result exceeds 75% of allowable error, the difference between any 2 results exceeds 4 times the peer group SD, or the mean SD index of all 5 results exceeds 1.5. As method quality increases from marginal to high, false rejections range from 16% to nearly zero, and the probability of detecting a shift equal to 2 times the intralaboratory SD ranges from 94% to 69%.


Clinical Chemistry | 1974

Criteria for Judging Precision and Accuracy in Method Development and Evaluation

James O. Westgard; R. Neill Carey; Svante Wold


Clinical Chemistry | 1997

Quality control for qualitative assays: quantitative QC procedure designed to assure analytical quality required for an ELISA of hepatitis B surface antigen

George A. Green; R. Neill Carey; James O. Westgard; Tami Carten; LeeAnn Shablesky; Daniel Achord; Eileen Page; Anh Van Le


Clinical Chemistry | 1974

Evaluation of the Adaptation of the Glucose Oxidase/Peroxidase-3-Methyl-2-benzothiazolinone hydrazone-N, N-Dimethylaniline Procedure to the Technicon "SMA 12/60," and Comparison with Other Automated Methods for Glucose

R. Neill Carey; Donald H. Feldbruegge; James O. Westgard


Clinical Chemistry | 1975

Separation of Creatine Kinase Isoenzymes by High-Pressure Liquid Chromatography

Paul J. Kudirka; Michael G. Busby; R. Neill Carey; E. Clifford Toren


Clinical Chemistry | 2000

Adding Value to Proficiency Testing Programs

George S. Cembrowski; R. Neill Carey


American Journal of Clinical Pathology | 1976

Assessment of the Serum Separator Tube as an Intermediate Storage Device with in the Laboratory

Ronald H. Laessig; David J. Hassemer; James O. Westgard; R. Neill Carey; Donald H. Feldbruegge; Thomas H. Schwartz


Archive | 1989

Laboratory quality management : QC [and] QA

George S. Cembrowski; R. Neill Carey


Labmedicine | 1989

Considerations for the Implementation of Clinically Derived Quality Control Procedures

George S. Cembrowski; R. Neill Carey


Labmedicine | 1975

Selecting Glucose Methods That Meet Your Laboratory Requirements

Elsa F. Quam; James O. Westgard; R. Neill Carey

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George S. Cembrowski

University of Wisconsin-Madison

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James O. Westgard

Oklahoma State Department of Health

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Donald H. Feldbruegge

Oklahoma State Department of Health

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Carl C. Garber

University of Wisconsin-Madison

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David J. Hassemer

Oklahoma State Department of Health

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E. Clifford Toren

University of Wisconsin-Madison

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Elsa F. Quam

University of Wisconsin-Madison

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Paul J. Kudirka

University of Wisconsin-Madison

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Ronald H. Laessig

Oklahoma State Department of Health

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Thomas H. Schwartz

Oklahoma State Department of Health

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