Evaluation of the Analytical Performance of Atellica CH 930 Automated Chemistry Analyzer
- Author:
Daewon KIM
1
;
Yonggeun CHO
;
Jooyoung CHO
;
Sun hee KIM
;
Sang Guk LEE
;
Jeong Ho KIM
Author Information
- Publication Type:Original Article
- Keywords: Atellica CH 930 Analyzer; Performance evaluation; Automated QC function
- MeSH: Appointments and Schedules; Aspartate Aminotransferases; Bilirubin; Calcium; Chemistry; Quality Control
- From:Laboratory Medicine Online 2019;9(3):133-145
- CountryRepublic of Korea
- Language:Korean
- Abstract: BACKGROUND: Recently, a new automated chemistry analyzer, Atellica CH930 (Siemens, Germany), was introduced. It automatically measures internal quality control (QC) materials according to a pre-determined schedule. For this purpose, the instrument has space for storage of QC materials. We evaluated the analytical performance of chemistry items by using the Atellica system. METHODS: The precision of 29 items was evaluated with three levels of QC materials with two storage methods. We stored the QC materials in the dedicated storage space in the instrument during the precision evaluation period. In addition, we aliquoted and stored the materials in the refrigerator, and then loaded the material in a timely manner. Linearity, carry-over, and agreement with current methods were also evaluated. RESULTS: The within-laboratory coefficient of variation (CV) of most items, except for total CO2 (tCO2), was within 5.0% in both QC storage methods without significant differences in CV between storage methods. The CV of tCO2 was 5.2%, 5.8%, and 5.1% at three different levels when the QC materials were stored in a dedicated space in the instrument. The linearity was acceptable, showing <5% nonlinearity. Although good agreement was observed for most items, some items, such as calcium, total bilirubin, aspartate transaminase, and chloride, showed unequivalent results. CONCLUSIONS: Atellica CH930 showed acceptable precision, linearity, and agreement in routine chemistry items. The automatic QC function using the storage device has no problem with stability or precision. It can reduce the manual process, allowing technicians to focus on reviewing the QC results and reporting reliable results.
