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Identifying Appropriate Reference Data Models for Comparative Effectiveness Research (CER) Studies Based on Data from Clinical Information Systems

机译:根据临床信息系统中的数据,确定用于比较有效性研究(CER)研究的适当参考数据模型

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Introduction: The need for a common format for electronic exchange of clinical data prompted federal endorsement of applicable standards. However, despite obvious similarities, a consensus standard has not yet been selected in the comparative effectiveness research (CER) community.Methods: Using qualitative metrics for data retrieval and information loss across a variety of CER topic areas, we compare several existing models from a representative sample of organizations associated with clinical research: the Observational Medical Outcomes Partnership (OMOP), Biomedical Research Integrated Domain Group, the Clinical Data Interchange Standards Consortium, and the US Food and Drug Administration.Results: While the models examined captured a majority of the data elements that are useful for CER studies, data elements related to insurance benefit design and plans were most detailed in OMOP's CDM version 4.0. Standardized vocabularies that facilitate semantic interoperability were included in the OMOP and US Food and Drug Administration Mini-Sentinel data models, but are left to the discretion of the end-user in Biomedical Research Integrated Domain Group and Analysis Data Model, limiting reuse opportunities. Among the challenges we encountered was the need to model data specific to a local setting. This was handled by extending the standard data models.Discussion: We found that the Common Data Model from the OMOP met the broadest complement of CER objectives. Minimal information loss occurred in mapping data from institution-specific data warehouses onto the data models from the standards we assessed. However, to support certain scenarios, we found a need to enhance existing data dictionaries with local, institution-specific information.
机译:简介:对电子交换临床数据的通用格式的需求促使联邦政府认可适用的标准。然而,尽管存在明显的相似之处,但在比较有效性研究(CER)社区中尚未选择共识标准。与临床研究相关的组织的代表性样本:观察医学成果合作伙伴关系(OMOP),生物医学研究集成领域小组,临床数据交换标准协会和美国食品和药物管理局。结果:虽然所研究的模型涵盖了大多数对于CER研究有用的数据元素,与保险利益设计和计划相关的数据元素在OMOP的CDM版本4.0中最详细。 OMOP和美国食品药品监督管理局迷你哨兵数据模型中包含促进语义互操作性的标准化词汇表,但最终用户可以在生物医学研究集成域组和分析数据模型中自行决定,从而限制了重用的机会。我们遇到的挑战之一是需要对本地设置特定的数据进行建模。这是通过扩展标准数据模型来处理的。讨论:我们发现OMOP的通用数据模型满足了CER目标的最广泛补充。将机构特定数据仓库中的数据映射到我们评估的标准的数据模型中时,信息损失最小。但是,为了支持某些情况,我们发现需要使用本地的,特定于机构的信息来增强现有的数据字典。

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