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使用美国国家临床实验室标准委员会C28-P提议的指南在临床实验室中确定参考区间。

Determination of reference intervals in the clinical laboratory using the proposed guideline National Committee for Clinical Laboratory Standards C28-P.

作者信息

Sasse E A

机构信息

Department of Pathology, Medical College of Wisconsin, Milwaukee County General Hospital 53226.

出版信息

Arch Pathol Lab Med. 1992 Jul;116(7):710-3.

PMID:1497442
Abstract

The Subcommittee on Reference Intervals of the National Committee for Clinical Laboratory Standards (NCCLS) has recently completed a proposed guideline, NCCLS Document C28-P, entitled "How to Define, Determine, and Utilize Reference Intervals in the Clinical Laboratory." This guideline document is an attempt to combine a concise set of procedures and recommendations, largely taken from the original literature, to form a standard, uniform, and reasonable protocol for determining population-based reference intervals. The intent of the guideline is to set forth the minimum requirements for the determination of a reliable and clinically useful reference interval. The subcommittee hopes the document will set a standard that upgrades the quality of reference intervals to a level worthy of their use in clinical medicine.

摘要

美国国家临床实验室标准委员会(NCCLS)参考区间小组委员会最近完成了一份拟议指南,即NCCLS文件C28 - P,题为《临床实验室如何定义、确定和使用参考区间》。该指南文件试图整合一套简洁的程序和建议,这些程序和建议主要取自原始文献,以形成一个用于确定基于人群的参考区间的标准、统一且合理的方案。该指南的目的是阐述确定可靠且临床有用的参考区间的最低要求。小组委员会希望该文件能设定一个标准,将参考区间的质量提升到值得在临床医学中使用的水平。

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