• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

作为常规患者茶碱检测准确性预测指标的能力验证测试表现

Proficiency test performance as a predictor of accuracy of routine patient testing for theophylline.

作者信息

Jenny R W, Jackson K Y

机构信息

Wadsworth Center for Laboratories and Research, New York State Department of Health, Albany 12201-0509.

出版信息

Clin Chem. 1993 Jan;39(1):76-81.

PMID:8419063
Abstract

Proficiency testing (PT) is pivotal in assessing laboratory qualifications for certification and licensure. PT is expected to typify routine assay performance and determine whether the laboratory is producing clinically useful test results. Conventional schemes use mail-distributed test specimens and are often criticized as measuring the best possible laboratory performance, principally because of special practices associated with processing PT specimens. We used on-site proficiency tests and split samples to evaluate the ability of conventional PT schemes to accurately characterize routine laboratory performance. Using 412 assays of theophylline, performed routinely by 200 laboratories and subsequently in a reference laboratory, we found that the predictive value of PT performance in assessing quality of routine testing was high (100% for predicting substandard reliability of routine patient testing and 94% for excluding substandard reliability of patient testing). The imprecision of interlaboratory PT results was equivalent whether testing was observed (hand-carried specimens) or unobserved (mail-distributed specimens). Many methods used for determining theophylline concentration in serum were highly automated, closed, and precise analytical systems. The performance characteristics of these analytical systems are not easily manipulated by the analyst for purposes of improving PT outcome, and PT by use of mail-distributed test specimens is effective for assessing intralaboratory performance.

摘要

能力验证(PT)对于评估实验室认证和许可资格至关重要。PT旨在代表常规检测性能,并确定实验室是否能产生临床有用的检测结果。传统方案使用邮寄分发的检测样本,常因主要与处理PT样本相关的特殊做法而被批评为衡量的是实验室的最佳可能性能。我们采用现场能力验证和分割样本,来评估传统PT方案准确描述常规实验室性能的能力。利用200个实验室常规进行的412次茶碱检测,随后在一个参考实验室进行检测,我们发现PT性能在评估常规检测质量方面的预测价值很高(预测常规患者检测的不合格可靠性为100%,排除患者检测的不合格可靠性为94%)。无论检测是被观察的(亲手递交样本)还是未被观察的(邮寄分发样本),实验室间PT结果的不精密度都是相当的。许多用于测定血清中茶碱浓度的方法都是高度自动化、封闭式且精确的分析系统。这些分析系统的性能特征不容易被分析人员为改善PT结果而操控,并且使用邮寄分发检测样本进行的PT对于评估实验室内部性能是有效的。

相似文献

1
Proficiency test performance as a predictor of accuracy of routine patient testing for theophylline.作为常规患者茶碱检测准确性预测指标的能力验证测试表现
Clin Chem. 1993 Jan;39(1):76-81.
2
Process capability and stability of analytical systems assessed from proficiency testing data.根据能力验证数据评估分析系统的过程能力和稳定性。
Clin Chem. 1994 May;40(5):723-8.
3
Proficiency testing linked to the national reference system for the clinical laboratory: a proposal for achieving accuracy.与临床实验室国家参考系统相关的能力验证:实现准确性的一项提议
Clin Chem. 1992 Jul;38(7):1260-7; discussion 1268-72.
4
Intra- and interlaboratory sources of imprecision in drug measurements by different techniques.不同技术进行药物测量时实验室内和实验室间不精密度的来源。
Clin Chem. 1993 May;39(5):851-5.
5
Matrix effects on proficiency testing materials. Impact on accuracy of cholesterol measurement in laboratories in the nation's largest hospital system.基质对能力验证材料的影响。对全国最大医院系统中各实验室胆固醇测量准确性的影响。
Arch Pathol Lab Med. 1993 Apr;117(4):345-51.
6
Certification of cholesterol measurements by the National Reference Method Laboratory Network with routine clinical specimens: effects of network laboratory bias and imprecision.国家参考方法实验室网络使用常规临床标本对胆固醇测量进行的认证:网络实验室偏差和不精密度的影响
Clin Chem. 1992 May;38(5):651-7.
7
Intralaboratory performance requirements necessary to pass proficiency testing: CAP-1990 vs CLIA-1967 (March 14, 1990) formats compared.通过能力验证所需的实验室内部性能要求:CAP - 1990与CLIA - 1967(1990年3月14日)格式对比
Clin Chem. 1992 Jun;38(6):895-903.
8
Proficiency testing performance: a case study with modeling.能力验证性能:一个建模案例研究
Clin Biochem. 2002 Sep;35(6):447-53. doi: 10.1016/s0009-9120(02)00337-5.
9
How good are clinical laboratories? An assessment of current performance.临床实验室的水平如何?当前绩效评估。
Clin Chem. 1992 Jul;38(7):1210-7; discussion 1218-25.
10
Review of actual proficiency-testing performance under CLIA '67 (March 14, 1990) rules: perspective from the first year's data.根据《1967年临床实验室改进法案》(1990年3月14日)规则对实际能力验证表现的回顾:基于第一年数据的视角。
Clin Chem. 1992 Jul;38(7):1254-9; discussion 1268-72.

引用本文的文献

1
Current landscape and new paradigms of proficiency testing and external quality assessment for molecular genetics.分子遗传学中能力验证和外部质量评估的现状和新范式。
Arch Pathol Lab Med. 2013 Jul;137(7):983-8. doi: 10.5858/arpa.2012-0311-RA.
2
Evaluation of mycology laboratory proficiency testing.真菌学实验室能力验证评估。
J Clin Microbiol. 1999 Jul;37(7):2297-305. doi: 10.1128/JCM.37.7.2297-2305.1999.