Changes in Total CO2 Measurement According to Reagent Cassette Rotation in Chemistry Autoanalyzers

被引:0
作者
Chung, Hee-Jung [1 ,2 ]
Lee, Woochang [1 ,2 ]
Chun, Sail [1 ,2 ]
Kang, So Young [3 ]
Lee, Woo In [3 ]
Park, Hae-Il [4 ]
Min, Won-Ki [1 ,2 ]
机构
[1] Univ Ulsan, Coll Med, Dept Lab Med, Seoul 138736, South Korea
[2] Asan Med Ctr, Seoul 138736, South Korea
[3] Kyung Hee Univ, Coll Med, EW Neo Med Ctr, Seoul, South Korea
[4] Catholic Univ, Coll Med, Seoul, South Korea
关键词
carbon dioxide assay; clinical chemistry automated analyzers; quality control; TOTAL CARBON-DIOXIDE; BLOOD; SERUM;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The quality control (QC) failure rate in the serum total carbon dioxide (TCO2) test increases at a higher rate than in other tests over time after calibration. The causes of the increased QC failure rate in the TCO2 test were examined. Using a TBA200RF analyzer (Toshiba Medical Systems), the TCO2 of the QC material was measured at 2-hr intervals and was found to decrease by up to 16.5% at 10 hr after calibration. In contrast, using the P-module and D-module analyzers (Roche Diagnostics), the TCO2 of the QC material did not change significantly during 10 hr after calibration. When the TCO2 level of the QC material was measured hourly over 5 hr with the TBA200FR analyzer while the reagent bottle was rotated at 0, 80, 120, 160, or 200 rpm, the rate of decline of TCO2, increased over time after calibration and with increasing reagent cassette rotation. Therefore, in a clinical laboratory using an automated analyzer with a rotating reagent cassette, it is necessary to set a limit to the calibration time interval in order to satisfy the QC goal.
引用
收藏
页码:150 / 154
页数:5
相关论文
共 7 条
  • [1] [Anonymous], 2004, EP5A2 NCCLS
  • [2] IFCC reference measurement procedure for substance concentration determination of total carbon dioxide in blood, plasma or serum
    Burnett, RW
    Covington, AK
    Fogh-Andersen, N
    Külpmann, WR
    Lewenstam, A
    Mas, AHJ
    VanKessel, AL
    Zijlstra, WG
    [J]. CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2001, 39 (03) : 283 - 288
  • [3] *CLIN LAB STAND I, 2001, C46A CLSI
  • [4] NORRIS KA, 1975, CLIN CHEM, V21, P1093
  • [5] RYDER KW, 1988, CLIN CHEM, V34, P1910
  • [6] UNGERER JPJ, 1990, CLIN CHEM, V36, P2093
  • [7] 2007, COMPREHENSIVE CHEM S