Division of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.
Mayo Clin Proc. 2012 Dec;87(12):1202-13. doi: 10.1016/j.mayocp.2012.08.012. Epub 2012 Nov 28.
The Rochester Epidemiology Project (REP) has maintained a comprehensive medical records linkage system for nearly half a century for almost all persons residing in Olmsted County, Minnesota. Herein, we provide a brief history of the REP before and after 1966, the year in which the REP was officially established. The key protagonists before 1966 were Henry Plummer, Mabel Root, and Joseph Berkson, who developed a medical records linkage system at Mayo Clinic. In 1966, Leonard Kurland established collaborative agreements with other local health care providers (hospitals, physician groups, and clinics [primarily Olmsted Medical Center]) to develop a medical records linkage system that covered the entire population of Olmsted County, and he obtained funding from the National Institutes of Health to support the new system. In 1997, L. Joseph Melton III addressed emerging concerns about the confidentiality of medical record information by introducing a broad patient research authorization as per Minnesota state law. We describe how the key protagonists of the REP have responded to challenges posed by evolving medical knowledge, information technology, and public expectation and policy. In addition, we provide a general description of the system; discuss issues of data quality, reliability, and validity; describe the research team structure; provide information about funding; and compare the REP with other medical information systems. The REP can serve as a model for the development of similar research infrastructures in the United States and worldwide.
罗切斯特流行病学项目(REP)拥有近半个世纪的综合医学记录链接系统,几乎涵盖了明尼苏达州罗切斯特市的所有居民。本文简要介绍了 1966 年之前和之后的 REP 历史,1966 年正是 REP 正式成立的一年。1966 年之前的关键人物是 Henry Plummer、Mabel Root 和 Joseph Berkson,他们在梅奥诊所开发了一个医学记录链接系统。1966 年,Leonard Kurland 与其他当地医疗服务提供商(医院、医生团体和诊所[主要是奥姆斯特德医疗中心])建立了合作协议,开发了一个覆盖奥姆斯特德县全部人口的医学记录链接系统,并从美国国立卫生研究院获得了资金支持。1997 年,L. Joseph Melton III 根据明尼苏达州的法律,引入了广泛的患者研究授权,以解决人们对医疗记录信息保密性的担忧。我们描述了 REP 的关键人物如何应对不断发展的医学知识、信息技术和公众期望与政策所带来的挑战。此外,我们还对系统进行了概述;讨论了数据质量、可靠性和有效性问题;描述了研究团队结构;提供了有关资金的信息;并将 REP 与其他医疗信息系统进行了比较。REP 可以作为美国和全球类似研究基础设施发展的典范。