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Clinical Trial
. 2012 Oct;19(10):1624-32.
doi: 10.1128/CVI.00294-12. Epub 2012 Aug 15.

Results of continuous monitoring of the performance of rubella virus IgG and hepatitis B virus surface antibody assays using trueness controls in a multicenter trial

Affiliations
Clinical Trial

Results of continuous monitoring of the performance of rubella virus IgG and hepatitis B virus surface antibody assays using trueness controls in a multicenter trial

Tamara Kruk et al. Clin Vaccine Immunol. 2012 Oct.

Abstract

We conducted a multicenter trial in Canada to assess the value of using trueness controls (TC) for rubella virus IgG and hepatitis B virus surface antibody (anti-HBs) serology to determine test performance across laboratories over time. TC were obtained from a single source with known international units. Seven laboratories using different test systems and kit lots included the TC in routine assay runs of the analytes. TC measurements of 1,095 rubella virus IgG and 1,195 anti-HBs runs were plotted on Levey-Jennings control charts for individual laboratories and analyzed using a multirule quality control (MQC) scheme as well as a single three-standard-deviation (3-SD) rule. All rubella virus IgG TC results were "in control" in only one of the seven laboratories. Among the rest, "out-of-control" results ranged from 5.6% to 10% with an outlier at 20.3% by MQC and from 1.1% to 5.6% with an outlier at 13.4% by the 3-SD rule. All anti-HBs TC results were "in control" in only two laboratories. Among the rest, "out-of-control" results ranged from 3.3% to 7.9% with an outlier at 19.8% by MQC and from 0% to 3.3% with an outlier at 10.5% by the 3-SD rule. In conclusion, through the continuous monitoring of assay performance using TC and quality control rules, our trial detected significant intra- and interlaboratory, test system, and kit lot variations for both analytes. In most cases the assay rejections could be attributable to the laboratories rather than to kit lots. This has implications for routine diagnostic screening and clinical practice guidelines and underscores the value of using an approach as described above for continuous quality improvement in result reporting and harmonization for these analytes.

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Figures

Fig 1
Fig 1
Comparison of rubella virus IgG trueness control measurement results for laboratories D (A) and A (B), both of which used the Abbott AxSYM instrument. The numbers within the control chart are lot numbers.
Fig 2
Fig 2
Anti-HBs trueness control measurement results for laboratory D, showing a trending effect. The numbers within the control chart are lot numbers.
Fig 3
Fig 3
Anti-HBs trueness control measurements for laboratory E, showing a trending effect associated with different lots of the test kit. The numbers within the control chart are lot numbers.

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