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: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary.
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National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary.

机译:美国国家临床生物化学实验室医学实践指南:通过串联质谱扩大新生儿筛查确定的代谢性疾病的后续检测;执行摘要。

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摘要

BACKGROUND: Almost all newborns in the US are screened at birth for multiple inborn errors of metabolism using tandem mass spectrometry. Screening tests are designed to be sufficiently sensitive so that cases are not missed. The NACB recognized a need for standard guidelines for laboratory confirmation of a positive newborn screen such that all babies would benefit from equal and optimal follow-up by confirmatory testing. METHODS: A committee was formed to review available data pertaining to confirmatory testing. The committee evaluated previously published guidelines, published methodological and clinical studies, clinical case reports, and expert opinion to support optimal confirmatory testing. Grading was based on guidelines adopted from criteria derived from the US Preventive Services Task Force and on the strength of recommendations and the quality of the evidence. Three primary methods of analyte measurement were evaluated for confirmatory testing including measurement of amino acids, organic acids, and carnitine esters. The committee graded the evidence for diagnostic utility of each test for the screened conditions. RESULTS: Ample data and experience were available to make strong recommendations for the practice of analyzing amino acids, organic acids, and acylcarnitines. Likewise, strong recommendations were made for the follow-up test menu for many disorders, particularly those with highest prevalence. Fewer data exist to determine the impact of newborn screening on patient outcomes in all but a few disorders. The guidelines also provide an assessment of developing technology that will fuel a refinement of current practice and ultimate expansion of the diseases detectable by tandem mass spectrometry. CONCLUSIONS: Guidelines are provided for optimal follow-up testing for positive newborn screens using tandem mass spectrometry. The committee regards these tests as reliable and currently optimal for follow-up testing. .
机译:背景:在美国,几乎所有新生儿在出生时都使用串联质谱法进行多重代谢先天性错误筛查。筛查测试被设计为足够敏感,因此不会遗漏病例。 NACB认识到需要实验室确认阳性筛查的标准指南,以便所有婴儿都可以通过确认性测试获得同等和最佳的随访。方法:成立了一个委员会,以审查与确认测试有关的可用数据。该委员会评估了以前发布的指南,发布的方法和临床研究,临床病例报告以及专家意见,以支持最佳的验证性测试。评分是根据美国预防服务工作组(US Preventive Services Task Force)制定的准则以及建议的强度和证据的质量进行的。评价了三种主要的分析物测量方法以进行确认性测试,包括氨基酸,有机酸和肉碱酯的测量。该委员会对筛选条件下每种测试的诊断效用进行了分级。结果:丰富的数据和经验可为分析氨基酸,有机酸和酰基肉碱的做法提供强有力的建议。同样,针对许多疾病,尤其是患病率最高的疾病,在随访测试菜单中也提出了强烈的建议。除少数疾病外,几乎没有数据可确定新生儿筛查对患者预后的影响。该指南还评估了正在开发的技术,这些技术将推动当前实践的完善,并最终扩展通过串联质谱法可检测的疾病。结论:提供了使用串联质谱法对阳性新生儿筛查进行最佳随访测试的指南。委员会认为这些测试是可靠的,目前是后续测试的最佳选择。 。

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