中华检验医学杂志
中華檢驗醫學雜誌
중화검험의학잡지
Chinese Journal of Laboratory Medicine
2015年
11期
742-745
,共4页
章晓燕%王薇%赵海建%张传宝%王治国
章曉燕%王薇%趙海建%張傳寶%王治國
장효연%왕미%조해건%장전보%왕치국
血红蛋白A,糖基化%实验室能力验证%质量控制%质量保证,卫生保健
血紅蛋白A,糖基化%實驗室能力驗證%質量控製%質量保證,衛生保健
혈홍단백A,당기화%실험실능력험증%질량공제%질량보증,위생보건
Hemoglobin A,glycosylated%Laboratory proficiency testing%Quality control%Quality assurance,health care
目的 分析我国糖化血红蛋白(HbA1c)正确度验证计划中不同检测系统的质量水平.方法 横断面调查.通过室间质评软件收集参加2014年第1次全国糖化血红蛋白正确度验证室间质评(EQA)实验室的HbA1c数据.对所有实验室检测结果按仪器进行分组统计,剔除小于5家实验室的检测系统数据后计算各组观察到的偏倚(Bias%)、变异系数(CV%)和西格玛值(σ),并将各组的Bias%和CV%绘制在室间质量评价西格玛图上;同时计算201411和201412两个样品的平均Bias%、平均CV%和加权σ.结果 123家实验室分为9个仪器小组;以6%为HbA1c的允许总误差,201411样品(靶值为5.4%)的平均Bias%为3.70%,平均CV为4.55%,加权西格码水平为0.51σ-;201412样品(靶值为7.8%)的平均Bias%为2.42%,平均CV为3.56%,加权西格码水平为1.24--.从西格玛图中可看出201411样品所有检测系统都未达到2,201412只有1个检测系统达到2σ-.结论 我国HbA1c许多检测系统的结果和参考测量程序赋予的靶值之间存在明显的偏倚,不精密度也存在较大的问题,采用室间质评西格玛图可提示需要改进检测方法的质量水平保证检测结果的可靠性,促使HbA1c更好地应用于临床.
目的 分析我國糖化血紅蛋白(HbA1c)正確度驗證計劃中不同檢測繫統的質量水平.方法 橫斷麵調查.通過室間質評軟件收集參加2014年第1次全國糖化血紅蛋白正確度驗證室間質評(EQA)實驗室的HbA1c數據.對所有實驗室檢測結果按儀器進行分組統計,剔除小于5傢實驗室的檢測繫統數據後計算各組觀察到的偏倚(Bias%)、變異繫數(CV%)和西格瑪值(σ),併將各組的Bias%和CV%繪製在室間質量評價西格瑪圖上;同時計算201411和201412兩箇樣品的平均Bias%、平均CV%和加權σ.結果 123傢實驗室分為9箇儀器小組;以6%為HbA1c的允許總誤差,201411樣品(靶值為5.4%)的平均Bias%為3.70%,平均CV為4.55%,加權西格碼水平為0.51σ-;201412樣品(靶值為7.8%)的平均Bias%為2.42%,平均CV為3.56%,加權西格碼水平為1.24--.從西格瑪圖中可看齣201411樣品所有檢測繫統都未達到2,201412隻有1箇檢測繫統達到2σ-.結論 我國HbA1c許多檢測繫統的結果和參攷測量程序賦予的靶值之間存在明顯的偏倚,不精密度也存在較大的問題,採用室間質評西格瑪圖可提示需要改進檢測方法的質量水平保證檢測結果的可靠性,促使HbA1c更好地應用于臨床.
목적 분석아국당화혈홍단백(HbA1c)정학도험증계화중불동검측계통적질량수평.방법 횡단면조사.통과실간질평연건수집삼가2014년제1차전국당화혈홍단백정학도험증실간질평(EQA)실험실적HbA1c수거.대소유실험실검측결과안의기진행분조통계,척제소우5가실험실적검측계통수거후계산각조관찰도적편의(Bias%)、변이계수(CV%)화서격마치(σ),병장각조적Bias%화CV%회제재실간질량평개서격마도상;동시계산201411화201412량개양품적평균Bias%、평균CV%화가권σ.결과 123가실험실분위9개의기소조;이6%위HbA1c적윤허총오차,201411양품(파치위5.4%)적평균Bias%위3.70%,평균CV위4.55%,가권서격마수평위0.51σ-;201412양품(파치위7.8%)적평균Bias%위2.42%,평균CV위3.56%,가권서격마수평위1.24--.종서격마도중가간출201411양품소유검측계통도미체도2,201412지유1개검측계통체도2σ-.결론 아국HbA1c허다검측계통적결과화삼고측량정서부여적파치지간존재명현적편의,불정밀도야존재교대적문제,채용실간질평서격마도가제시수요개진검측방법적질량수평보증검측결과적가고성,촉사HbA1c경호지응용우림상.
Objective To investigate the results of different measuring procedures of hemoglobin A1c (HbA1c) trueness verification scheme in China.Methods Cross sectional survey.The data were collected via the External Quality Assessment (EQA) software from laboratories participated in the First HbA1c trueness verification EQA.Then the collected data were divided into several groups based on laboratory instruments and the data from less than 5 group were excluded.The observed imprecision, bias and sigma (σ) were calculated and the bias% and CV% were drew in the sigma chart.The average bias%, CV% and weighted average σ of each level were also calculated.Results Total 123 laboratories were divided into 9 groups and setting 6% as the Allowable Total Error, the average bias%, CV% and weighted average σ of 201411 (target value was 5.4%) were 3.70%, 4.55% and 0.51 respectively σ, of 201412 (target value was 7.8%)were 2.42% , 3.56% and 1.24σ respectively.None of the group achieved the 2σ quality of 201411, and 1 group achieved the 2σ quality of 201412.Conclusions There are obvious biases among the results of many measuring systems and the target value assigned by reference measuring procedures of HbA1c, as well as the imprecision.The Sigma External Quality Assessment Chart is a visual tool, indicating that the quality of measuring systems necessitate improvement therefore to ensure the reliability of results and make better use of HbA1c in clinical application.