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心血管风险新标志物评估标准:美国心脏协会的科学声明

Criteria for evaluation of novel markers of cardiovascular risk: a scientific statement from the American Heart Association.

作者信息

Hlatky Mark A, Greenland Philip, Arnett Donna K, Ballantyne Christie M, Criqui Michael H, Elkind Mitchell S V, Go Alan S, Harrell Frank E, Hong Yuling, Howard Barbara V, Howard Virginia J, Hsue Priscilla Y, Kramer Christopher M, McConnell Joseph P, Normand Sharon-Lise T, O'Donnell Christopher J, Smith Sidney C, Wilson Peter W F

出版信息

Circulation. 2009 May 5;119(17):2408-16. doi: 10.1161/CIRCULATIONAHA.109.192278. Epub 2009 Apr 13.

Abstract

There is increasing interest in utilizing novel markers of cardiovascular disease risk, and consequently, there is a need to assess the value of their use. This scientific statement reviews current concepts of risk evaluation and proposes standards for the critical appraisal of risk assessment methods. An adequate evaluation of a novel risk marker requires a sound research design, a representative at-risk population, and an adequate number of outcome events. Studies of a novel marker should report the degree to which it adds to the prognostic information provided by standard risk markers. No single statistical measure provides all the information needed to assess a novel marker, so measures of both discrimination and accuracy should be reported. The clinical value of a marker should be assessed by its effect on patient management and outcomes. In general, a novel risk marker should be evaluated in several phases, including initial proof of concept, prospective validation in independent populations, documentation of incremental information when added to standard risk markers, assessment of effects on patient management and outcomes, and ultimately, cost-effectiveness.

摘要

人们对利用心血管疾病风险的新型标志物越来越感兴趣,因此,有必要评估其使用价值。本科学声明回顾了当前风险评估的概念,并提出了风险评估方法批判性评价的标准。对新型风险标志物进行充分评估需要合理的研究设计、具有代表性的高危人群以及足够数量的结局事件。对新型标志物的研究应报告其增加标准风险标志物所提供预后信息的程度。没有单一的统计指标能提供评估新型标志物所需的所有信息,因此应报告鉴别力和准确性的指标。标志物的临床价值应通过其对患者管理和结局的影响来评估。一般来说,新型风险标志物应在几个阶段进行评估,包括初步概念验证、在独立人群中的前瞻性验证、添加到标准风险标志物时增量信息的记录、对患者管理和结局影响的评估,最终是成本效益评估。

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