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Sysmex CS-5100全自动凝血分析仪的性能评价 被引量:2

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摘要 目的对Sysmex CS-5100全自动凝血分析仪进行全面性能评价。方法通过2014年1月在Sysmex CS-5100全自动凝血分析仪上测定活化部分凝血活酶时间(APTT)、血浆凝血酶原时间(PT)、凝血酶时间(TT)和纤维蛋白原(FIB),对仪器进行精密度、准确度、线性、检测限、携带污染率进行评价。结果批内和批间最大变异系数(CV)为6.75%,符合厂家规定(CV<10%),仪器精密度良好。准确性试验测定结果均在厂家规定范围内,仪器准确性良好。FIB的相关系数r为0.9857(>0.975),符合要求。FIB的检测限为0.28g/L,CV为3.45%,符合厂家规定(CV<20%),携带污染率均低于10%,符合要求。结论 Sysmex CS-5100全自动凝血分析仪具有较高的精密度和准确度,较宽的检测范围,样本间携带污染率低的特点,能够为临床提供准确的检测结果。
作者 王旭
出处 《中国卫生产业》 2015年第1期149-150,共2页 China Health Industry
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  • 1陆红兵,孙文旦,王妍,郁寿仙.STA-Compact型全自动血凝仪的性能评价[J].血栓与止血学,2005,11(4):174-175. 被引量:6
  • 2栾桂红.法国STAGO全自动血液凝固仪评价[J].国际检验医学杂志,2007,28(1). 被引量:3
  • 3唐宁,曹文静,夏汛生,张碧玉.ACL TOP全自动血凝分析系统的性能评价[J].医疗设备信息,2007,22(2):48-51. 被引量:17
  • 4National Committee for Clinical Laboratory Standards. Evaluation of precision performance of quantitative measurement methds; approved guideline [ S ]. EP5-A2, NCCLS, 2004.
  • 5Clinical and Laboratory Standards Institute.H57-A Protocol for the evaluation,validation,and implementation of coagulometers;approved guideline[S].Wayne,PA:CLSI,2008.
  • 6Clinical and Laboratory Standards Institute.P7-A2 Interference testing in clinical chemistry; approved guideline-second edition[S].Wayne,PA:CLSI,2005.
  • 7Clinical and Laboratory Standards Institute.AUTO 8-A Managing and validating laboratory information systems; approved guideline[S].Wayne,PA:CLSI,2006.
  • 8Clinical and Laboratory Standards Institute.GP19-A2 Laboratory instruments and data management systems:design of software.User Interfaces and end-user software systems validation,operation,and monitoring; approved guideline-second edition[S].Wayne,PA:CLSI,2003.
  • 9Clinical and Laboratory Standards Institute.H49-A Point-of-care monitoring of anticoagulation therapy; approved guideline[S].Wayne,PA:CLSI,2004.
  • 10U.S.Department of Health and Human Services.Guideline for isolation precautions:preventing transmission of infectious agents in healthcare settings 2007[EB/OL].[2007-11-27].http://www.guideline.gov.

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  • 1NCCLS. Defining, Establishing, and Verifying Reference In- tervals in the Clinical Laboratory [ M ] Approve Guideline- Third Edition. Wayne, PA, USA : NCCLS,2010.
  • 2NCCLS. EP15-A2 User demonstration of performance for precision and accuracy; approved guideline [ S ]. Wayne, PA, USA : NCCLS,2004.
  • 3NCCLS. EP5-A Evaluation of precision performance of quantitative measurement methods : approved guideline [ S ]. Wayne, PA, USA : NCCLS, 2004.
  • 4NCCLS. Evaluation of the Linearity of Quantitative Measure- ment Procedures: A Statistical Approach; Approved Guide- line [ S 3. Wayne, PA, USA : NCCLS,2004.
  • 5NCCLS. C28-A2 How to define and determine refrence intervals in the clinical laboratory : approved guideline [ S ]. Wayne, PA, USA : NCCLS ,2000.
  • 6NCCLS. EP6-A Evaluation of the linearity of quantitative an- alytical methods : approved guideline [ S ]. Wayne, PA. USA: NCCLS, 2003.
  • 7Clinical and Laboratory Standards Institute.Evaluation of the Linearity of Quantitative Analytical Methods:EP6-ACLSI:2004[S].
  • 8徐益恒,李劲榆,马各富,邰文琳.全自动血凝仪ACL TOP700性能评价[J].国际检验医学杂志,2013,34(3):354-356. 被引量:10
  • 9郭国明.全自动血凝仪的性能评价及应用要求[J].安徽卫生职业技术学院学报,2013,12(2):101-102. 被引量:2
  • 10何新发,李燕妮.比较Sysmex CS5100与Sysmex CA1500全自动凝血分析仪凝血四项的检测[J].国际检验医学杂志,2014,35(20):2830-2831. 被引量:9

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