Setting process control limits for enzyme tests in serum

被引:2
作者
Lott, JA [1 ]
机构
[1] Ohio State Univ, Med Ctr, Dept Pathol, Columbus, OH 43210 USA
关键词
laboratory variability; medical needs criteria; proficiency testing; quality control; reference sample method;
D O I
10.1080/00365519950185283
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
With the advent of much more precise laboratory equipment, the use of performance-based standard deviations for enzymes, e.g; those based on the precision of the laboratory during a period of "satisfactory performance", is not appropriate; it leads to overly rigid precision limits and unnecessary repeat assays, and is wasteful of resources. Testing for the commonly used serum enzymes does not require tight precision given how enzyme data are viewed by most clinicians. Other ways to set process control limits all have some arbitrary content; however, this need not prevent their use. Laboratorians must choose the approach that is appropriate for their laboratory and medical staff to meet medically perceived needs.
引用
收藏
页码:527 / 530
页数:4
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