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移植病毒载量检测中不同检测方法间变异性的持续挑战。

Persistent Challenges of Interassay Variability in Transplant Viral Load Testing.

作者信息

Hayden R T, Caliendo A M

机构信息

Department of Pathology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA

Department of Medicine, Warren Alpert Medical School of Brown University, Providence, Rhode Island, USA.

出版信息

J Clin Microbiol. 2020 Sep 22;58(10). doi: 10.1128/JCM.00782-20.

Abstract

While quantification of viruses that cause important infections in transplant recipients has been the standard of care for years, important challenges related to standardization remain. The issues are wide ranging, and until they are adequately addressed, the full impact of viral load testing regarding clinical management decisions will not be realized. This review focuses on a broad array of problems, including the lack of available FDA-approved/cleared tests, limited uptake of international standards, accurate quantification of secondary standards, specific assay characteristics, and commutability. Though some of these topics are nuanced, taken together they greatly influence the clinical utility of testing. For example, it has not been possible to define thresholds that predict the risk of developing disease and determine significant changes in serial viral load values for a given patient. Moreover, the utility of international guidelines may be limited due to the lack of a standardized assay. By summarizing the issues, the hope is that commercial companies, regulatory agencies, and professional societies can come together to advance the field and solve these problems.

摘要

多年来,对导致移植受者发生重要感染的病毒进行定量检测一直是医疗标准,但在标准化方面仍存在重大挑战。这些问题涉及面广泛,在它们得到充分解决之前,病毒载量检测对临床管理决策的全部影响将无法实现。本综述重点关注一系列广泛的问题,包括缺乏美国食品药品监督管理局(FDA)批准/许可的检测方法、国际标准的采用有限、二级标准的准确定量、特定检测方法的特性以及互换性。尽管其中一些主题较为细微,但综合起来它们对检测的临床实用性有很大影响。例如,尚未能够确定预测发病风险的阈值,也无法确定给定患者连续病毒载量值的显著变化。此外,由于缺乏标准化检测方法,国际指南的实用性可能会受到限制。通过总结这些问题,希望商业公司、监管机构和专业协会能够共同努力推动该领域发展并解决这些问题。

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