Background: We report an evaluation of the Menarini/ARKRAY ADAMS A1c HA-8180V analyser (HA-8180V), the fifth generation Menarini/ARKRAY ion-exchange HPLC for the measurement of HbA(1c).
Methods: We evaluated the analytical performance, the measurement of haemoglobin variants and the performance in comparison to major analytical methods.
Results: Within-run, between-run and total CV were 0.2%, 0.4% and 0.7% at low HbA(1c) concentrations and 0.2%, 0.2% and 0.4% at high HbA(1c) concentrations, respectively. Trueness revealed a maximum deviation of 0.8 mmol/mol (IFCC units) or 0.1% (NGSP units) over the relevant analytical range. Linearity, carry-over and linear drift were excellent. Labile-HbA(1c), carbamylated haemoglobin, icteric samples and variation in hematocrit did not affect HbA(1c) outcome. Haemoglobin variants AS, AC and F do not affect HbA(1c) outcome and are explicitly identified and correctly quantified. HbA(1c) can not be measured in samples with AE and AD, but these variants are identified correctly. In comparison to other methods used at present, the HA-8180V shows excellent performance.
Conclusions: The HA-8180V performs at a high level and is fit for any clinical application.
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http://dx.doi.org/10.1515/CCLM.2011.096 | DOI Listing |
Clin Chem Lab Med
April 2011
European Reference Laboratory, Streekziekenhuis Koningin Beatrix, Winterswijk, The Netherlands.
Background: We report an evaluation of the Menarini/ARKRAY ADAMS A1c HA-8180V analyser (HA-8180V), the fifth generation Menarini/ARKRAY ion-exchange HPLC for the measurement of HbA(1c).
Methods: We evaluated the analytical performance, the measurement of haemoglobin variants and the performance in comparison to major analytical methods.
Results: Within-run, between-run and total CV were 0.
Clin Chem
June 1997
Department of Clinical Biochemistry, Royal London Hospital, Whitechapel, UK.
We describe a multinational evaluation of the Menarini-Arkray HA 8140 hemoglobin (Hb) A1c analyzer, which utilizes a high degree of automation, including bar code reading, cap piercing, and whole-blood sampling. With-in- and between-batch CVs were < 2%. Linearity was confirmed throughout the working range of the analyzer.
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