Performance of a new hepatitis C assays on the Bayer ADVIA Centaur® immunoassay system

Clinical Laboratory

Volumn 50, Issue 1-2, 2004, Pages 75-82

  Denoyel, Gérard ^a   van Helden, Josef ^b   Bauer, Richard ^c   Preisel Simmons, Barbara ^c  

^a LMM Laboratoire Marcel Merieux   (France)

^b Laboratory Dr Stein/Partners   (Germany)

^c BAYER CORPORATION   (United States)

Author keywords

ADVIA Centaur; Diagnostic sensitivity; Diagnostic specificity; Hepatitis C virus (HCV); Performance evaluation; Seroconversion panels

Indexed keywords

HEPATITIS C ANTIBODY;

ANTIBODY DETECTION; ARTICLE; AUTOMATION; BLOOD ANALYSIS; BLOOD DONOR; CHEMOLUMINESCENCE; CONTROLLED STUDY; EUROPE; HEPATITIS C; HEPATITIS C VIRUS; HOSPITAL PATIENT; HUMAN; IMMUNOASSAY; INTERMETHOD COMPARISON; MAGNETIC SEPARATION; MAJOR CLINICAL STUDY; MARKETING; QUALITY CONTROL; SENSITIVITY AND SPECIFICITY; SEROCONVERSION; TASK PERFORMANCE;

AUTOANALYSIS; BLOOD DONORS; CHEMILUMINESCENT MEASUREMENTS; GENOTYPE; HEPATITIS C; HEPATITIS C ANTIGENS; HUMANS; IMMUNOASSAY; IMMUNOMAGNETIC SEPARATION; REAGENT KITS, DIAGNOSTIC; SEROLOGIC TESTS;

HEPATITIS C VIRUS; RNA VIRUSES;

EID: 1442329698     PISSN: 14336510     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Doerr HW. Viral infections. In: Thomas L, editor. Clinical Laboratory Diagnostics. Th-Books, Frankfurt, 1998; 1218-59.
2. Richter SS. Laboratory assays for diagnosis and management of hepatitis C virus infection. J Clin Microbiol 2002; 40: 4407-12.
3. Hendriks HA, Kortlandt W, Verweij WM. Standardized comparison of processing capacity and efficiency of five new-generation immunoassay analyzers. Clin Chem 2000; 46: 105-11.
4. Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices. Official Journal of the European Communities 1998; L331:1-37.
5. Commission decision on common technical specifications for in vitro-diagnostic medical devices. Official Journal of the European Communities 2002; L 131:17-30.
6. NCCLS Document EP5-A - Evaluation of precision performance of clinical chemistry devices; Approved Guideline - Second Edition (1999).