B-131 从混合样本水平得出平均西格玛水平的谬误

IF 7.1 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY Clinical chemistry Pub Date : 2024-10-02 DOI:10.1093/clinchem/hvae106.492
Z BROOKS
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引用次数: 0

摘要

背景 西格玛衡量的是现有样本平均值与最接近的分析性能标准或允许误差极限之间的 SD(Z 值)数。作者和软件程序通常测量每个质控样本的西格玛指标,但使用平均西格玛来比较方法和选择质控策略。这种做法会导致高估或低估所报告的误差数量,并选择不恰当的质控策略。方法 创建数据样本,以产生 3.0、4.5 和 6.0 的西格玛值。使用 Microsoft Excel 函数 NORMSDIST 将西格玛值转换为每百万患者错误数的百分比。NORMSINV 用于将每百万患者的错误数转换为西格玛值。结果 A. 六西格玛代表一种失败率为 0.000001% 或每百万患者 ASP/TEa 失败 0.001 次的方法。B. 三西格玛代表一种故障率为 0.135% 或每百万患者 ASP/TEa 故障次数为 1,350 次的方法。C. 样本 A 和 B 的平均西格玛值为 4.5s,平均误差率为 0.0675%,即每百万患者中有 675 例 ASP/TEa 失败。D. 用 NORMSINV 函数将 0.0675% 的误差率转换为 3.21 的 sigma 值。E. 真正的 4.5 西格玛方法的失败率为 0.00034%,即每百万患者中有 3.4 例 ASP/TEa 失败。结论 提出平均西格玛值的西格玛研究低估了报告的真实错误数量。更科学正确的做法是报告所报告的错误数或根据平均错误数报告平均西格玛值。如果用一个西格玛代表两个或多个数据集,实验室专业人员应谨慎解释西格玛研究和出版物。
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B-131 The fallacy of average sigma levels from mixed sample levels
Background Sigma measures the number of SDs (z-value) from the existing sample mean to the nearest analytical performance standard or allowable error limit. Authors and software programs often measure sigma metrics for each QC sample but use an average sigma to compare methods and select QC strategies. That practice leads to dramatic over or under-estimation of the number of errors reported and the selection of inappropriate QC strategies. Methods Data samples were created to produce sigma values of 3.0, 4.5, and 6.0. Microsoft Excel function NORMSDIST was used to convert sigma to percent to number of errors per million patients. NORMSINV was used to convert the number of errors per million patients to sigma. Results A. Six sigma represents a method with a failure rate of 0.000001% or 0.001 failures of ASP/TEa per million patients. B. Three sigma represents a method with a failure rate of 0.135 percent or 1,350 failures of ASP/TEa per million patients. C. While the average sigma value of samples A and B was 4.5s, the average error rate was 0.0675 percent or 675 failures of ASP/TEa per million patients. D. An error rate was 0.0675 percent converts with the NORMSINV function to a sigma of 3.21. E. A true 4.5 sigma method would have a failure rate of 0.00034 percent or 3.4 failures of ASP/TEa per million patients. Conclusions Sigma studies that present an average sigma value underestimate the true number of errors reported. It would be more scientifically correct to either report the number of errors reported or to report the average sigma value based on the average number of errors. Laboratory professionals should interpret sigma studies and publications cautiously if a single sigma is used to represent two or more data sets.
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来源期刊
Clinical chemistry
Clinical chemistry 医学-医学实验技术
CiteScore
11.30
自引率
4.30%
发文量
212
审稿时长
1.7 months
期刊介绍: Clinical Chemistry is a peer-reviewed scientific journal that is the premier publication for the science and practice of clinical laboratory medicine. It was established in 1955 and is associated with the Association for Diagnostics & Laboratory Medicine (ADLM). The journal focuses on laboratory diagnosis and management of patients, and has expanded to include other clinical laboratory disciplines such as genomics, hematology, microbiology, and toxicology. It also publishes articles relevant to clinical specialties including cardiology, endocrinology, gastroenterology, genetics, immunology, infectious diseases, maternal-fetal medicine, neurology, nutrition, oncology, and pediatrics. In addition to original research, editorials, and reviews, Clinical Chemistry features recurring sections such as clinical case studies, perspectives, podcasts, and Q&A articles. It has the highest impact factor among journals of clinical chemistry, laboratory medicine, pathology, analytical chemistry, transfusion medicine, and clinical microbiology. The journal is indexed in databases such as MEDLINE and Web of Science.
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