首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines for Use of Tumor Markers in Clinical Practice: Quality Requirements
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National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines for Use of Tumor Markers in Clinical Practice: Quality Requirements

机译:美国国家临床生物化学研究院实验室医学实践指南中使用肿瘤标记物的质量要求

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Background: This report presents updated National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines summarizing quality requirements for the use of tumor markers.Methods: One subcommittee developed guidelines for analytical quality relevant to serum and tissue-based tumor markers in current clinical practice. Two other subcommittees formulated recommendations particularly relevant to the developing technologies of microarrays and mass spectrometry.Results: Prerequisites for optimal use of tumor markers in routine practice include formulation of the correct clinical questions to ensure selection of the appropriate test, adherence to good clinical and laboratory practices (e.g., minimization of the risk of incorrect patient and/or specimen identification, tube type, or timing), use of internationally standardized and well-characterized methods, careful adherence to manufacturer instructions, and proactive and timely reactions to information derived from both internal QC and proficiency-testing specimens. Highly desirable procedures include those designed to minimize the risk of the reporting of erroneous results attributable to interferences such as heterophilic antibodies or hook effects, to facilitate the provision of informative clinical reports (e.g., cumulative and/or graphical reports, appropriately derived reference intervals, and interpretative comments), and when possible to integrate these reports with other patient information through electronic health records. Also mandatory is extensive validation encompassing all stages of analysis before introduction of new technologies such as microarrays and mass spectrometry. Provision of high-quality tumor marker services is facilitated by dialogue involving researchers, diagnostic companies, clinical and laboratory users, and regulatory agencies.Conclusions: Implementation of these recommendations, adapted to local practice, should encourage optimization of the clinical use of tumor markers.
机译:背景:本报告介绍了最新的《美国国家临床生物化学研究院实验室医学操作指南》,概述了使用肿瘤标志物的质量要求。方法:一个小组委员会制定了当前临床实践中与血清和基于组织的肿瘤标志物相关的分析质量指南。另外两个小组委员会提出了与微阵列和质谱技术发展特别相关的建议。结果:在常规实践中最佳使用肿瘤标志物的前提条件包括制定正确的临床问题,以确保选择适当的测试,坚持良好的临床和实验室做法(例如,最大程度地减少错误地识别患者和/或样本,管类型或时机的风险),使用国际标准化且特征明确的方法,认真遵守制造商的说明以及对源自两者的信息进行积极及时的反应内部质量控制和能力测试标本。高度理想的程序包括旨在最大程度地减少因干扰(例如,异源抗体或钩子效应)引起的错误结果报告风险的程序,以便于提供信息丰富的临床报告(例如累积和/或图形报告,适当得出的参考区间,和解释性评论),并在可能的情况下通过电子健康记录将这些报告与其他患者信息整合在一起。在引入新技术(如微阵列和质谱)之前,还必须进行广泛的验证,包括分析的所有阶段。研究人员,诊断公司,临床和实验室用户以及监管机构之间的对话有助于提供高质量的肿瘤标志物服务。结论:根据当地实际情况实施这些建议应鼓励优化肿瘤标志物的临床使用。

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