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External quality assessment of the genetic testings for hematopoietic tumor, CML

机译:造血肿瘤,CML基因检测的外部质量评估

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Genetic testings are commonly employed in various fields of clinical medicine and the test items performed at clinical laboratories are increasing rapidly in number. They are utilized to make early and/or definite diagnoses of infectious diseases, leukemia, cancers and molecular inherited diseases and also to monitor the progress of the diseases. However, these genetic testings except for infectious diseases have been developed independently at each clinical laboratory and the test results obtained at each laboratory are not always compatible each other. Under these situations it is widely expected to construct advanced genetic testing systems that can supply standardized data at any of domestic and international clinical laboratories. For the period from April, 1999 to March, 2002 three major clinical laboratories, SRL, Inc., BML, Inc. and MBC, Inc., were consigned by JBA (Japan Bioindustry Association) to collaborate in standardizing the evaluation methods for genetic testing systems among the clinical laboratories. The aim of the study is to develop the standardized genetic testing systems and to propose them as international standard operational procedures to the ISO/TC212 working group. Although one of the most important issues for standardization is the external quality assessment, they have not been carried out in reality. In this study we evaluated the difference of the genetic testing results obtained during the year of 2000 and 2001 among the clinical laboratories. The genetic testings for hematopoietic tumor, CML were selected to be evaluated since they are widely accepted as clinically useful tests.
机译:基因检测通常用于临床医学的各个领域,并且在临床实验室执行的检测项目数量正在迅速增加。它们可用于对传染病,白血病,癌症和分子遗传性疾病进行早期和/或确定的诊断,还可以监测疾病的进展。但是,这些传染病除外的基因检测已在每个临床实验室独立开发,并且在每个实验室获得的检测结果并不总是相互兼容的。在这种情况下,人们普遍期望构建先进的基因检测系统,该系统可以在国内外任何一个临床实验室提供标准化数据。在1999年4月至2002年3月期间,JBA(日本生物产业协会)委托了三个主要的临床实验室,SRL,Inc.,BML,Inc.和MBC,Inc.进行合作,以标准化基因检测的评估方法临床实验室之间的系统。该研究的目的是开发标准化的基因检测系统,并将其作为国际标准操作程序建议给ISO / TC212工作组。尽管标准化最重要的问题之一是外部质量评估,但实际上尚未进行。在这项研究中,我们评估了临床实验室在2000年和2001年获得的基因检测结果的差异。选择对造血系统肿瘤(CML)的基因测试进行评估,因为它们被广泛接受为临床上有用的测试。

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