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口腔健康的规范方法:标准、规范和指南。

Normative Approaches for Oral Health: Standards, Specifications, and Guidelines.

机构信息

Department of Conservative Dentistry and Periodontology, University Hospital Regensburg, Regensburg, Germany.

Department of Periodontology, University of Bern, Bern, Switzerland.

出版信息

J Dent Res. 2022 May;101(5):489-494. doi: 10.1177/00220345211049695. Epub 2021 Oct 25.

Abstract

Normative approaches have been developed with the aim of providing high-quality methods and strict criteria that, when applied correctly, lead to reliable results. Standards, specifications, and guidelines are needed to facilitate exchange of goods or information and secure comparability of data derived from different laboratories and sources. They are available along the whole flow from study development to test selection, study conduct, and reporting and are widely used for the evaluation of medical devices, market approval, and harmonization of terms and devices. Standards are developed by specific national and international organizations or by dedicated interest groups, mainly scientists in their respective fields. ISO (International Organization for Standardization) standards are developed following stringent regulations, and groups of experts formulate such standards. They should come from different areas (multistakeholder approach) to have as much and as broad input as possible and to avoid single-interest dominance. However, the presence of academia in such groups has been comparatively low. There is a clear need and responsibility of the oral health community to participate in the development of normative documents to provide methodological knowledge and experience, balance the interests of other stakeholders, and finally improve oral health. This will help to ensure that rapidly advancing fields of research, such as the oral health impacts of COVID-19 or the application of artificial intelligence in dentistry, benefit from standardization of approaches and reporting.

摘要

规范方法已经发展起来,目的是提供高质量的方法和严格的标准,正确应用这些方法和标准可得出可靠的结果。需要标准、规范和指南来促进货物或信息的交换,并确保从不同实验室和来源获得的数据具有可比性。这些标准和指南贯穿研究开发、试验选择、研究实施以及报告的整个流程,广泛用于医疗器械的评估、市场准入以及术语和器械的协调统一。标准由特定的国家和国际组织或专门的利益集团制定,主要由各自领域的科学家组成。ISO(国际标准化组织)标准是按照严格的规定制定的,专家组制定这些标准。它们应该来自不同领域(多利益相关者方法),以尽可能广泛地获取和避免单一利益的主导地位。然而,学术界在这些团体中的参与相对较少。口腔健康界有明确的需要和责任参与规范性文件的制定,以提供方法学知识和经验,平衡其他利益相关者的利益,最终改善口腔健康。这将有助于确保像 COVID-19 对口腔健康的影响或人工智能在牙科中的应用等快速发展的研究领域从方法和报告的标准化中受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f31d/9024015/a88a3f21b800/10.1177_00220345211049695-fig1.jpg

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