[1]章晓燕,王 薇,何法霖,等.全国网织红细胞计数 参考区间和决定限现状调查与分析[J].现代检验医学杂志,2016,31(03):158-161.[doi:10.3969/j.issn.1671-7414.2016.03.045]
 ZHANG Xiao-yan,WANG Wei,HE Fa-lin,et al.Investigation and Analysis of Reference Intervals and Decision Limits of Reticulocyte Count in China[J].Journal of Modern Laboratory Medicine,2016,31(03):158-161.[doi:10.3969/j.issn.1671-7414.2016.03.045]
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全国网织红细胞计数 参考区间和决定限现状调查与分析()

《现代检验医学杂志》[ISSN:/CN:]

卷:
第31卷
期数:
2016年03期
页码:
158-161
栏目:
质量控制·实验室管理
出版日期:
2016-06-15

文章信息/Info

Title:
Investigation and Analysis of Reference Intervals and Decision Limits of Reticulocyte Count in China
作者:
章晓燕,王 薇,何法霖,钟 堃,王治国
北京医院 卫生部临床检验中心 北京市临床检验工程技术研究中心,北京 100730
Author(s):
ZHANG Xiao-yan,WANG Wei,HE Fa-lin,ZHONG Kun,WANGZhi-guo
National Center for Clinical Laboratories,Beijing Engineering Research Center of Laboratory Medicine,Beijing Hospital,Beijing 100730,China
关键词:
网织红细胞计数 参考区间 决定限
分类号:
R446.111
DOI:
10.3969/j.issn.1671-7414.2016.03.045
文献标志码:
A
摘要:
目的 调查目前中国网织红细胞计数参考区间的来源、上下限分布以及决定限的现状。方法 利用基于Web方式的室间质量评价软件系统,收集参加2014年网织红细胞计数参考区间调查的实验室参考区间上下限、临床决定水平、来源情况、方法原理、仪器和试剂等相关信息。按照仪器对各实验室进行分组,然后使用SPSS19.0软件对各组结果进行统计描述。结果 共276家实验室回报了有效结果。参考区间来源中所占比例依次为《全国临床检验操作规程》(53.99%)、仪器厂家说明书(16.30%)、教科书(9.78%)、试剂厂家说明书(9.06%)等。决定限来源中所占比例依次为《全国临床检验操作规程》(56.06%)、仪器厂家说明书(16.67%)、教科书(7.58%)、试剂厂家说明书(7.58%)等。不同组间的参考区间上下限以及临床决定水平的中位数与均值较为接近,但P2.5和P97.5差异较大。仅有45.65%和48.48%的实验室在使用参考区间和决定限前对其进行了验证。参考区间下限和决定限在不同组间无明显差异(P>0.05),但参考区间上限在不同仪器组间差异具有统计学意义(P<0.001)。结论 中国网织红细胞参考区间现状不尽如人意,应建立适应中国大多实验室和主要检测仪器的参考区间和决定限,为网织红细胞技术的标准化工作提供参考。
Abstract:
Objective To investigate and analyze the current situation of reference intervals and decision limits of reticulocyte count inChina.Methods The information related to upper/lower limits,decision limits,data resources,method principles,instruments and reagents of reticulocyte count in 2014 was collected via the external quality assessment software system based on website.The participants were divided according to their methods and instruments.The SPSS 19.0 was used for conducting the data analysis and statistics of results for each group.Results There were 276 laboratories submitting the valid results.The major resources for reference intervals came from national guide to clinical laboratory procedures(53.99%),instructions of instrument manufacturers(16.30%),textbook(9.78%),instructions of reagents manufacturers(9.06%)and others.The major resources for decision limits were national guide to clinical laboratory procedures(56.06%),instructions of instrument manufacturers(16.67%),textbook(7.58),instructions of reagents manufacturers(7.58%)and others.The medians and averages of upper/lower limits and decision limits among subgroups were close,whereasthe P2.5 and P97.5 were significant discrepancies.Only 45.65% and 48.48% of participant laboratories had verified reference intervals and decision limits before clinic use.The lower limits and decision limits among subgroups had nostatistical difference(P>0.05),where as the upper limits of different instrument groups had significant differences(P<0.001).Conclusion The current situation of reference intervals and decision limits of reticulocyte count is unsatisfactory.It is certain to establish auniformed reference interval and decision limits for reticulocyte count,which provides a reference for the standardization of reticulocyte count testing.

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备注/Memo

备注/Memo:
基金项目:北京市自然科学基金资助项目(7143182),北京医院课题资助(BJ-2015-025)。 作者简介:章晓燕(1992-),女,在读研究生,研究方向:实验室管理学。 通讯作者:王治国,E-mail:zgwang@nccl.org.cn。
更新日期/Last Update: 2016-06-25