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尿液化学检测——系列2。实验室间比对计划的5年经验。

The urine chemistry survey--series 2. 5 years' experience with an interlaboratory comparison program.

作者信息

Weaver D K, Glenn G C

机构信息

Department of Pathology, Williamsport (Pa) Hospital.

出版信息

Arch Pathol Lab Med. 1989 Jul;113(7):713-22.

PMID:2472782
Abstract

We have reviewed 5 years' experience with the College of American Pathologists Urine Chemistry Survey--Series 2. Analytes studied include aldosterone, total free catecholamines, the fractionated catecholamines norepinephrine, epinephrine, and dopamine, total catecholamines, estriol, 5-hydroxyindoleacetic acid, 17-ketogenic steroids, 17-ketosteroids, vanillylmandelic acid, cortisol, metanephrines, coproporphyrin, and uroporphyrin. Interlaboratory precision achieved by participants did not reach levels reported by various investigators, but their studies do not reflect actual clinical laboratory conditions. The intralaboratory analytical precision may be adequate for clinical diagnosis but better interlaboratory agreement must await the preparation of standards verified by definitive analyses. Biases introduced by the use of many different standards probably are the origin of mediocre interlaboratory proficiency testing performance.

摘要

我们回顾了美国病理学家学会尿液化学调查系列2的5年经验。所研究的分析物包括醛固酮、总游离儿茶酚胺、儿茶酚胺的分级成分去甲肾上腺素、肾上腺素和多巴胺、总儿茶酚胺、雌三醇、5-羟吲哚乙酸、17-生酮类固醇、17-酮类固醇、香草扁桃酸、皮质醇、间甲肾上腺素、粪卟啉和尿卟啉。参与者所达到的实验室间精密度未达到不同研究者报告的水平,但他们的研究并未反映实际临床实验室条件。实验室内分析精密度可能足以用于临床诊断,但要获得更好的实验室间一致性,必须等待经权威分析验证的标准品的制备。使用许多不同标准品所引入的偏差可能是实验室间能力验证表现平平的根源。

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