国际检验医学杂志
國際檢驗醫學雜誌
국제검험의학잡지
INTERNATIONAL JOURNAL OF LABORATORY MEDICINE
2014年
16期
2224-2225
,共2页
室内质量控制%甲状腺素%皮质醇%促甲状腺激素
室內質量控製%甲狀腺素%皮質醇%促甲狀腺激素
실내질량공제%갑상선소%피질순%촉갑상선격소
internal quality control%thyroxine%cortisol%thyroid stimulating hormone
目的:研究定量免疫分析检测项目的室内质量控制设计程序,为临床实验室免疫分析提供最合适的室内质量控制规则。方法以甲状腺素、皮质醇和促甲状腺激素3个定量检测项目为例,通过重复性试验得到方法的变异系数,作为方法不精密度的评估,再通过方法比对得到偏倚,评估方法的正确度,然后根据变异系数和偏倚在操作过程规范(OPSpecs)图中标出操作点的位置,选择各定量免疫分析检测项目最合适的质量控制规则。结果当甲状腺素决定水平为0.0644 mmol/L 时,N =6,分析质量保证(AQA)为90%的操作过程规范(OPSpecs)图提示13s/(2of3)2s/R4s/31s/6 x 和13s/(2of3)2s/R4s/31s 两种多规则方法。当皮质醇的决定水平为0.735μmol/L,N =3,AQA 为90%时,可以采用13s/(2of3)2s/R4s/31s 、12.5s 或13s/(2of3)2s/R4s 3种方法。当促甲状腺激素为高浓度水平,N =4,AQA 为50%时,最好使用31s/22s/R4s/41s 多规则;当为低浓度水平,N =2,AQA 为50%时,可以使用13s/22s/R4s 规则。结论使用操作过程规范图可以为定量免疫分析检测项目选择合适的室内质量控制设计程序。
目的:研究定量免疫分析檢測項目的室內質量控製設計程序,為臨床實驗室免疫分析提供最閤適的室內質量控製規則。方法以甲狀腺素、皮質醇和促甲狀腺激素3箇定量檢測項目為例,通過重複性試驗得到方法的變異繫數,作為方法不精密度的評估,再通過方法比對得到偏倚,評估方法的正確度,然後根據變異繫數和偏倚在操作過程規範(OPSpecs)圖中標齣操作點的位置,選擇各定量免疫分析檢測項目最閤適的質量控製規則。結果噹甲狀腺素決定水平為0.0644 mmol/L 時,N =6,分析質量保證(AQA)為90%的操作過程規範(OPSpecs)圖提示13s/(2of3)2s/R4s/31s/6 x 和13s/(2of3)2s/R4s/31s 兩種多規則方法。噹皮質醇的決定水平為0.735μmol/L,N =3,AQA 為90%時,可以採用13s/(2of3)2s/R4s/31s 、12.5s 或13s/(2of3)2s/R4s 3種方法。噹促甲狀腺激素為高濃度水平,N =4,AQA 為50%時,最好使用31s/22s/R4s/41s 多規則;噹為低濃度水平,N =2,AQA 為50%時,可以使用13s/22s/R4s 規則。結論使用操作過程規範圖可以為定量免疫分析檢測項目選擇閤適的室內質量控製設計程序。
목적:연구정량면역분석검측항목적실내질량공제설계정서,위림상실험실면역분석제공최합괄적실내질량공제규칙。방법이갑상선소、피질순화촉갑상선격소3개정량검측항목위례,통과중복성시험득도방법적변이계수,작위방법불정밀도적평고,재통과방법비대득도편의,평고방법적정학도,연후근거변이계수화편의재조작과정규범(OPSpecs)도중표출조작점적위치,선택각정량면역분석검측항목최합괄적질량공제규칙。결과당갑상선소결정수평위0.0644 mmol/L 시,N =6,분석질량보증(AQA)위90%적조작과정규범(OPSpecs)도제시13s/(2of3)2s/R4s/31s/6 x 화13s/(2of3)2s/R4s/31s 량충다규칙방법。당피질순적결정수평위0.735μmol/L,N =3,AQA 위90%시,가이채용13s/(2of3)2s/R4s/31s 、12.5s 혹13s/(2of3)2s/R4s 3충방법。당촉갑상선격소위고농도수평,N =4,AQA 위50%시,최호사용31s/22s/R4s/41s 다규칙;당위저농도수평,N =2,AQA 위50%시,가이사용13s/22s/R4s 규칙。결론사용조작과정규범도가이위정량면역분석검측항목선택합괄적실내질량공제설계정서。
Objective To study the internal quality control(IQC)designing procedure of the quantitative immunoassay testing i-tem to provide the most suitable IQC rule for the clinical laboratory immunoassay.Methods 3 quantitative detection items of thy-roxine,cortisol and thyroid stimulating hormone were taken for examples.The coefficient of variation(CV)of the method was ob-tained by the repeatability test for evaluating the methodological imprecision.Inaccuracy(bias)was obtained by the methods com-parison.The accuracy of the method was evaluated.Then the most suitable IQC rule for each quantitative detection item was select-ed by plotting the location of the operating point on the normalized operational process specifications(OPSpecs)chart according to CV and bias.Results Two multirule methods of 1 3s/(2of3)2s/R4s/3 1s/6 x and 1 3s/(2of3)2s/R4s/3 1s were identified when the oper-ating point was plotted on the normalized OPSpecs chart for N =6 and 90% analytical quality assurance(AQA)at the thyroxine de-cisive level of 0.064 4 mmol/L.When the cortisol decisive level was 0.735 μmol/L,the normalized OPSpecs chart for N =3 with 90%AQA showed the three solutions of 1 3s/(2of3)2s/R4s/3 1s ,1 2 .5s ,and 1 3s/(2of3)2s/R4s as for thyroid stimulating hormone,3 1s/2 2s/R4s/41s multirole procedure was the best choice for N =4,50%AQA at the upper control level,and the N =2 chart with 50%AQA showed a multirole procedure with 1 3s/2 2s/R4s at the lower control level.Conclusion The suitable internal quality control de-signing procedure of the quantitative immunoassay testing item can be selected by using the OPSpecs chart.