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Applying a common data model to Asian databases for multinational pharmacoepidemiologic studies: opportunities and challenges

机译:将通用数据模型应用于亚洲数据库进行跨国药物流行病学研究:机遇与挑战

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Objective: The goal of the Asian Pharmacoepidemiology Network is to study the effectiveness and safety of medications commonly used in Asia using databases from individual Asian countries. An efficient infrastructure to support multinational pharmacoepidemiologic studies is critical to this effort. Study design and setting: We converted data from the Japan Medical Data Center database, Taiwan’s National Health Insurance Research Database, Hong Kong’s Clinical Data Analysis and Reporting System, South Korea’s Ajou University School of Medicine database, and the US Medicare 5% sample to the Observational Medical Outcome Partnership common data model (CDM). Results: We completed and documented the process for the CDM conversion. The coordinating center and participating sites reviewed the documents and refined the conversions based on the comments. The time required to convert data to the CDM varied widely across sites and included conversion to standard terminology codes and refinements of the conversion based on reviews. We mapped 97.2%, 86.7%, 92.6%, and 80.1% of domestic drug codes from the USA, Taiwan, Hong Kong, and Korea to RxNorm, respectively. The mapping rate from Japanese domestic drug codes to RxNorm (70.7%) was lower than from other countries, and we mapped remaining unmapped drugs to Anatomical Therapeutic Chemical Classification System codes. Because the native databases used international procedure coding systems for which mapping tables have been established, we were able to map 90% of diagnosis and procedure codes to standard terminology codes. Conclusion: The CDM established the foundation and reinforced collaboration for multinational pharmacoepidemiologic studies in Asia. Mapping of terminology codes was the greatest challenge, because of differences in health systems, cultures, and coding systems.
机译:目的:亚洲药物流行病学网络的目标是使用来自各个亚洲国家的数据库来研究在亚洲常用的药物的有效性和安全性。支持多国药物流行病学研究的有效基础设施对这项工作至关重要。研究设计和设置:我们将来自日本医学数据中心数据库,台湾国家国民健康保险研究数据库,香港的临床数据分析和报告系统,韩国的Ajou大学医学院的数据库以及美国5%的Medicare样本转换为数据。观察性医疗成果合作伙伴通用数据模型(CDM)。结果:我们完成并记录了CDM转换过程。协调中心和参与站点审核了文档,并根据评论对转换进行了细化。将数据转换为CDM所需的时间因站点而异,其中包括转换为标准术语代码以及根据评论进行转换的改进。我们分别将来自美国,台湾,香港和韩国的97.2%,86.7%,92.6%和80.1%的国内药品代码映射到RxNorm。从日本国内药品法规到RxNorm的映射率(70.7%)低于其他国家/地区,我们将剩余的未映射药品映射到“解剖治疗化学分类系统”法规。因为本机数据库使用已建立映射表的国际过程编码系统,所以我们能够将90%以上的诊断和过程代码映射到标准术语代码。结论:清洁发展机制为亚洲跨国药物流行病学研究奠定了基础,并加强了合作。由于卫生系统,文化和编码系统的差异,映射术语代码是最大的挑战。

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