Risk of false positive hepatitis C virus RNA due to sample to sample carryover on an automated hematology analyzer
Author:
Affiliation:
1. Department of Pathology, University Hospitals Case Medical Center, Cleveland , OH , United States of America
Publisher
Walter de Gruyter GmbH
Subject
Biochemistry (medical),Clinical Biochemistry,General Medicine
Link
https://www.degruyter.com/document/doi/10.1515/cclm-2012-0274/pdf
Reference10 articles.
1. Schlain B, Frush H, Pennington C, Osikowicz G, Ford F. Two stage procedure for evaluating interassay carryover on random-access instruments. Clin Chem 1996;42:725–31.8653898
2. Schlain B, Krouwer JS. Multi-factor designs II. A design for identifying instruments with sample-to-sample carryover and drift. Clin Chem 1989;35:2118–20.
3. Clinical Laboratory Standards Institute. Preliminary evaluation of quantitative clinical laboratory methods. EP10-A2. Wayne, PA: CLSI, 2009.
4. College of American Pathologists Laboratory Accreditation Program. 2011. Microbiology Checklist MIC 32708, MIC 63322, MIC 63324.
5. Armbruster DA, Alexander DB. Sample to sample carryover: a source of analytical laboratory error and its relevance to integrated clinical chemistry/immunoassay systems. Clin Chim Acta 2006;373:37–43.16777083
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