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新鲜血比对方法在血液分析仪室内质量控制中的应用
引用本文:王文娟,王佩佩,李雪芬,葛霞琴,童明,郭希超.新鲜血比对方法在血液分析仪室内质量控制中的应用[J].浙江大学学报(医学版),2008,37(1):88-92,96.
作者姓名:王文娟  王佩佩  李雪芬  葛霞琴  童明  郭希超
作者单位:浙江大学医学院,附属第一医院检验科,浙江,杭州,310003
摘    要:目的:利用新鲜血样本以比对方法对血液分析仪全血细胞计数进行室内质量控制。方法:选择性良好、规范化操作的血液分析仪为参比仪,用该仪器定值的健康人新鲜血校准比对血液分析仪(比对仪),进行为期3个月比对实验,建立比对仪比对参数WBC、RBC、Hb、HCT、PLT低、中、高值相对偏差范围。每工作日选取门诊患者比对参数低、中、高值至少2个水平新鲜血常规标本,将比对仪和参比仪检测结果进行比对,计算WBC、RBC、Hb、HCT、PLT相对偏差;以日期为横坐标,相对偏差为纵坐标,将相对偏差范围设置为±2 s,在实验室信息系统中建立新鲜血比对质控图,以制定的新鲜血比对质量控制规则对相对偏差进行判断、分析,对失控情况作出相应处理,保证仪器正常运作。结果:以建立的方法进行室内质量控制,2006年比对仪WBC、RBC、Hb、HCT、PLT低、中、高水平比对样本测定结果相对偏差分别为(0.75±2.964)%、(1.19±2.488)%、(1.43±2.439)%;(-0.39±1.327)%、(-0.26±1.297)%、(-0.35±1.095)%;(-0.43±1.393)%、(-0.17±1.139)%、(0.24±1.166)%;(-0.43±1.362)%、(-0.36±1.381)%、(-0.57±1.299)%;(-0.93±4.330)%、(0.04±4.118)%、(-0.41±4.149)%。2006年该比对仪作为第二台仪器参加美国病理学家学会血细胞分析能力验证,WBC、RBC、HGB、HCT、PLT测定值与靶值的偏倚范围分别为(-0.5~5.1)%、(-1.0~1.6)%、(-1.7~1.4)%、(-1.5~1.3)%、(-4.5~7.4)%。结论:该方法能方便、经济地对血液分析仪进行有效的质量控制。

关 键 词:血液化学分析/仪器和设备  质量控制  血细胞计数/仪器和设备  血液  新鲜血  比对方法  血液分析仪  室内质量控制  应用  blood  analyzer  quality  control  internal  method  comparison  经济  偏倚  靶值  测定值  能力验证  血细胞分析  学会  理学家  国病
文章编号:1008-9292(2008)01-0088-05
收稿时间:2007-02-25
修稿时间:2007-12-06

Application of comparison method in internal quality control of hematology analyzer by using fresh blood
WANG Wen-juan,WANG Pei-pei,LI Xue-fen,GE Xia-qin,TONG Ming,GUO Xi-chao.Application of comparison method in internal quality control of hematology analyzer by using fresh blood[J].Journal of Zhejiang University(Medical Sciences),2008,37(1):88-92,96.
Authors:WANG Wen-juan  WANG Pei-pei  LI Xue-fen  GE Xia-qin  TONG Ming  GUO Xi-chao
Institution:Department of Clinical Laboratory, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China.
Abstract:OBJECTIVE: To investigate the comparison method on internal control of hematology analyzer by using fresh blood. METHODS: The hematology analyzer with well function was selected as the reference analyzer, fresh blood samples from healthy subjects were measured by reference analyzer and the values were used to calibrate compared hematology analyzers. The acceptable limits of relative deviation of WBC,RBC, HGB,HCT, PLT were established by comparative experiments during three months. The results of fresh blood samples from patients with low/medium/high levels measured by compared analyzer were compared with those from reference analyzer, the relative deviation of WBC, RBC, HGB, HCT, PLT was calculated respectively. The internal quality control charts in laboratory information system were established, with date as x-axis, relative deviation as y-axis. The acceptable relative deviation limits were set to be +/-2 s, and to be used for laboratory quality control. RESULT: The relative deviation of WBC, RBC, HGB, HCT, PLT with high, medium, low levels were(0.75+/-2.964)%, (1.19+/-2.488)%,(1.43+/-2.439)%; (-0.39+/-1.327)%, (-0.26+/-1.297)%, (-0.35+/-1.095)%?(-0.43+/-1.393)%, (-0.17+/-1.139)%, (0.24+/-1.166)%?(-.43+/-1.362)%, (-0.36+/-1.381)%, (-0.57+/-1.299)%?(-0.93+/-4.330)%,(0.04+/-4.118)%, (-0.41+/-4.149)%, respectively in 2006. As the second instrument, the compared analyzer was involved in College of American Pathologists Proficiency Testing with satisfactory results, the bias of WBC,RBC, HGB, HCT, PLT were within (-0.5 approximately 5.1)%, (-1.0 approximately 1.6)%, (-1.7 approximately 1.4)%, (-1.5 approximately 1.3)%, (-4.5 approximately 7.4)%, respectively. CONCLUSION: The quality control on compared hematology analyzer can be effectively, conveniently and economically performed using this method.
Keywords:Blood chemical analysis/instrum  Quality control  Blood cell count/instrum  Blood
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