The Institute of Clinical Medicine, Tallinn, Estonia.
J Proteome Res. 2011 Jan 7;10(1):97-100. doi: 10.1021/pr1007784. Epub 2010 Dec 14.
The nation-wide electronic health record database acts as an interoperable repository of health data obtained throughout citizen contacts with health care providers. This system improves accessibility for citizens and researchers to health data with the ability to assign context to disease development. In that system, individual patients who are members of the large population-based health database can be assessed as individuals or as a population in prospective studies of prospective diseases.
全国性的电子健康记录数据库充当了一个可互操作的健康数据存储库,这些数据是在公民与医疗保健提供者接触过程中获得的。该系统提高了公民和研究人员获取健康数据的便利性,并能够为疾病的发展赋予背景。在该系统中,作为大型基于人群的健康数据库的成员的个体患者可以作为个体或作为前瞻性疾病的前瞻性研究中的人群进行评估。