Abstract

Abstract Background CLSI EP23A states that “At the least, the ability of the QC procedures to detect medically allowable error should be evaluated.” It also defines that “The QC strategy using QC samples should include the following for each measuring system: Methods Eighty QC sample mean and SD values were compared to Peer Means and TEa limits for 14 routine chemistry analytes and four cardiac markers tested in December 2022. The number of patient results was normalized to 200 and 60 per day for routine and cardiac; the number reported before the first QC flag after a simulated shift to a 5% error was calculated using CatalystQC software for seven incremental scenarios of quality control beginning with [A] Original QC rules (1-3s/2-2s), chart limits, frequency (once per day), analytical bias & SD; [B] Westgard Rules based on sigma values; [C] Westgard QC frequency; [D] Chart means & SDs set to measured values; [E] Improved bias and/or SD where advised by CatalystQC software; [F] Single CatalystQC™ rules; [G] QC bracketed at the end of each day. Results The number of patients at risk decreased with each component of the QC process. Observed and advised number of QC samples per year was inconsistent. Conclusion Selecting Westgard rules and frequency alone will not reduce patient risk significantly. Assigning QC chart values to recent mean and SD and improving analytical bias and SD have the most impact on reduction of patient risk. Catalyst QC single rules are more effective than Westgard rules. Bracketing QC with verified-effective QC will reduce patient risk to zero.

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