机构地区:[1]连云港市第二人民医院检验科,江苏连云港222006
出 处:《中华临床实验室管理电子杂志》2020年第1期36-40,共5页Chinese Journal of Clinical Laboratory Management(Electronic Edition)
基 金:南京医科大学康达学院科研发展基金重点项目(KD2019KYJJZD010)。
摘 要:目的探讨六西格玛(6σ)在评价内分泌项目分析性能上的应用价值。方法收集本实验室2018年10月至2019年3月室内质控(IQC)数据以及2018年第二次和2019年第一次室间质量评价(EQA)数据,应用四个不同来源的性能规范作为质量目标、室内质控长期累计的变异系数作为精密度和室间质评项目的百分差值作为偏倚分别评估内分泌项目的σ水平,分析不同质量目标对内分泌项目的σ值所产生的差异,并制定个性化的室内质控方案。评估σ值<6项目的质量目标指数(QGI),为实验室的质量改进提供实施方案。结果不同的质量目标,各项目的σ分布存在显著差异,依据国家EQA评价标准、生物学变异导出"适当的"质量规范和美国临床实验室标准化协会(CLSI)推荐的质量规范,σ值≥6项目的比例分布于20.0%~35.4%之间;依据西班牙EQA评价标准,则未见σ值≥6的项目。依据各项目的分析性能,制定个性化的室内质控方案:总三碘甲状腺原氨酸(TT3)、促甲状腺素(TSH)、黄体生成素(LH)和睾酮(T)选择单规则13s进行质量控制;催乳素(PRL)选择多规则13s/22s/R4s进行质量控制;游离甲状腺素(FT4)选择多规则13s/22s/R4s/41s进行质量控制;游离三碘甲状腺原氨酸(FT3)、总甲状腺素(TT4)、雌二醇(E2)、卵泡刺激素(FSH)和孕酮(P)选择多规则13s/22s/R4s/41S/8X进行质量控制。依据我国EQA评价标准,FT3、FT4、TT4、E2、FSH、P、PRL项目均需优先改进精密度。结论 6σ能够客观评价内分泌项目的分析性能,并促进实验室检测质量的持续改进。Objective To investigate the application value of Six Sigma in the evaluation of endocrine project analysis performance.Methods The data of internal quality control(IQC)from October 2018 to March 2019 and the data of external quality assessment(EQA)from second time in 2018 and first time in 2019 were collected respectively.Four different sources of performance specifications were used as quality goals,and the long-term cumulative coefficient of variation of IQC were used as precision and the percentage difference of EQA were used as bias to evaluateσlevels of endocrine items andσvalues of endocrine items with different quality objectives.Meanwhile,individualized IQC scheme was formulated.In addition,the quality target index(QGI)of items withσvalue below 6 were evaluated and the plan for laboratory quality improvement was provided.Results According to the national EQA evaluation standard,biological variation,“appropriate”quality standard and quality standard recommended by CLSI are derived.The proportion of projects withσvalue≥6 is between 20.0%and 35.4%;While,according to the Spanish EQA standard,no analytes withσvalue more than 6 were found.According to the analytical performance of each project,a personalized IQC scheme was developed:total triiodothyronine(TT3),thyroid stimulating hormone(TSH),luteinizing hormone(LH)and testosterone(T)were selected for single rule 13s for quality control,prolactin(PRL)was selected multiple rule 13s/22s/R4s for quality control,free thyroxine(FT4) was selected multiple rule 13s/22s/R4s/41s for quality control, free triiodothyronine (FT3), total thyroxine(TT4), estradiol (E2), follicle stimulating hormone (FSH) and progesterone (P) were selected multiple rule13s/22s/R4s/41S/8X for quality control. According to the Chinese EQA standard, the precision of FT3, FT4,TT4, E2, FSH, P and PRL should be improved firstly. Conclusion Six Sigma can reasonably evaluate theanalytical performance of the endocrine project and promote the continuous improvement of laboratorytest quality
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