Creating a Molecular Atmosphere, Phase 5

IF 1 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY
S. Wallace
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引用次数: 0

Abstract

As mentioned in previous articles in this series, product inserts are available with most FDA-approved assays. These product inserts contain information about the product as well as explain processes and procedures approved by the manufacturer of the assay. Included in these procedures are quality control (QC) recommendations. Some FDA-approved assays have QC material included in the packaging of test materials; others suggest from whom to purchase the quality control material and provide recommendations on how to use it. For all of the assays that we perform on the Infinity (Thermo Fisher Scientific, Waltham, MA) instrument, we routinely perform external QC on new lots and new shipments. All of these assays are FDA-approved, qualitative, and include a built-in internal control for every patient test that is performed. Because the internal control is present, we are not required to perform external QC procedures with every patient specimen. The external controls used for these assays are purchased from a manufacturer and can be used directly or after a simple dilution is made. The assays we perform on the SmartCycler (Cepheid, Sunnyvale, CA) are laboratory developed; therefore, control materials are not commercially available in ready-to-use form. Clinical Laboratory Standards Institute (CLSI) and College of American Pathologist (CAP) guidelines suggest that laboratorians ensure that a control is present throughout the entirety of a patient testing procedure. If an internal control cannot be present from start to finish, external-control material must be included in every patient-testing procedure. For herpes simplex virus (HSV) external control, we purchase stock virus from a manufacturer. We grow the virus in shell vials, in a similar manner that we would use for controls when setting up HSV cultures. This growth of virus in shell vials takes anywhere from 3 to 5 days to yield a 90% or greater cytopathic effect (CPE). … [↵][1]* To whom correspondence should be addressed. E-mail: stephanie.e.wallace{at}osfhealthcare.org [1]: #xref-corresp-1-1
创造分子气氛,第五阶段
正如本系列之前的文章中提到的,大多数fda批准的检测方法都有产品说明书。这些产品说明书包含有关产品的信息,以及解释检测制造商批准的过程和程序。这些程序包括质量控制(QC)建议。一些fda批准的检测方法在测试材料的包装中包含QC材料;其他人建议从谁那里购买质量控制材料,并提供如何使用的建议。对于我们在Infinity (Thermo Fisher Scientific, Waltham, MA)仪器上进行的所有分析,我们通常会对新批次和新发货进行外部QC。所有这些检测都是fda批准的,定性的,并且包括对每个患者进行的检测的内置内部控制。由于存在内部控制,我们不需要对每个患者标本执行外部质量控制程序。用于这些测定的外部对照物是从制造商处购买的,可以直接使用,也可以在简单稀释后使用。我们在SmartCycler (Cepheid, Sunnyvale, CA)上进行的检测是实验室开发的;因此,控制材料在商业上没有现成的可用形式。临床实验室标准协会(CLSI)和美国病理学家学会(CAP)的指导方针建议,实验室人员应确保在整个患者检测过程中都有对照。如果内部控制不能从头到尾存在,外部控制材料必须包含在每个患者检测程序中。对于单纯疱疹病毒(HSV)的外部控制,我们从制造商处购买库存病毒。我们在壳小瓶中培养病毒,以类似于我们在建立HSV培养时用于对照的方式。这种病毒在壳小瓶中的生长需要3到5天的时间才能产生90%或更高的细胞病变效应(CPE)。[1]信函应寄给谁?电子邮件:stephanie.e.wallace{at}osfhealthcare.org [1]: #xref-corresp-1-1
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Labmedicine
Labmedicine 医学-医学实验技术
CiteScore
2.50
自引率
0.00%
发文量
155
审稿时长
>12 weeks
期刊介绍: Lab Medicine is a peer-reviewed biomedical journal published quarterly by the ASCP and Oxford University Press. The journal invites submission of manuscripts on topics related to clinical chemistry and microbiology, hematology, immunology, transfusion medicine, molecular diagnostics, cytology, histology, and laboratory administration and management. Original research, reviews, and case reports are considered for publication. Lab Medicine is indexed (under the title Laboratory Medicine) by the National Library of Medicine and is included in the PubMed database.
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