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临床实验室测量程序协调路线图。

Roadmap for harmonization of clinical laboratory measurement procedures.

机构信息

Virginia Commonwealth University, Richmond, VA, USA.

出版信息

Clin Chem. 2011 Aug;57(8):1108-17. doi: 10.1373/clinchem.2011.164012. Epub 2011 Jun 15.

Abstract

Results between different clinical laboratory measurement procedures (CLMP) should be equivalent, within clinically meaningful limits, to enable optimal use of clinical guidelines for disease diagnosis and patient management. When laboratory test results are neither standardized nor harmonized, a different numeric result may be obtained for the same clinical sample. Unfortunately, some guidelines are based on test results from a specific laboratory measurement procedure without consideration of the possibility or likelihood of differences between various procedures. When this happens, aggregation of data from different clinical research investigations and development of appropriate clinical practice guidelines will be flawed. A lack of recognition that results are neither standardized nor harmonized may lead to erroneous clinical, financial, regulatory, or technical decisions. Standardization of CLMPs has been accomplished for several measurands for which primary (pure substance) reference materials exist and/or reference measurement procedures (RMPs) have been developed. However, the harmonization of clinical laboratory procedures for measurands that do not have RMPs has been problematic owing to inadequate definition of the measurand, inadequate analytical specificity for the measurand, inadequate attention to the commutability of reference materials, and lack of a systematic approach for harmonization. To address these problems, an infrastructure must be developed to enable a systematic approach for identification and prioritization of measurands to be harmonized on the basis of clinical importance and technical feasibility, and for management of the technical implementation of a harmonization process for a specific measurand.

摘要

不同临床实验室测量程序(CLMP)之间的结果应在临床有意义的范围内等效,以便能够根据疾病诊断和患者管理的临床指南进行最佳使用。当实验室测试结果既没有标准化也没有协调时,同一临床样本可能会得到不同的数值结果。不幸的是,一些指南是基于特定实验室测量程序的测试结果制定的,而没有考虑到各种程序之间存在差异的可能性或可能性。当这种情况发生时,来自不同临床研究调查的数据的聚合以及适当的临床实践指南的制定将存在缺陷。如果没有认识到结果既没有标准化也没有协调,可能会导致错误的临床、财务、监管或技术决策。已经为存在主要(纯物质)参考物质并且/或者已经开发出参考测量程序(RMP)的几个可测量物质完成了 CLMP 的标准化。然而,由于对可测量物质的定义不充分、对可测量物质的分析特异性不足、对参考物质的可替代性关注不足以及缺乏系统的协调方法,因此尚未协调没有 RMP 的临床实验室程序。为了解决这些问题,必须开发一个基础设施,以便能够根据临床重要性和技术可行性,对要协调的可测量物质进行系统的识别和优先级排序,并对特定可测量物质的协调技术实施进行管理。

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