首页> 外文期刊>Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation >UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking
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UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking

机译:URAPLE:大数据分析研究数据平台,使用常规电子健康记录和标准化生物管理改善心肌病的患者的护理

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Despite major advances in our understanding of genetic cardiomyopathies, they remain the leading cause of premature sudden cardiac death and end-stage heart failure in persons under the age of 60years. Integrated research databases based on alarge number of patients may provide ascaffold for future research. Using routine electronic health records and standardised biobanking, big data analysis on alarger number of patients and investigations are possible. In this article, we describe the UNRAVEL research data platform embedded in routine practice to facilitate research in genetic cardiomyopathies. Eligible participants with proven or suspected cardiac disease and their relatives are asked for permission to use their data and to draw blood for biobanking. Routinely collected clinical data are included in a research database by weekly extraction. Atext-mining tool has been developed to enrich UNRAVEL with unstructured data in clinical notes. Thus far, 828 individuals with amedian age of 57years have been included, 58% of whom are male. All data are captured in atemporal sequence amounting to atotal of 18,565 electrocardiograms, 3619echocardiograms, data from over 20,000 radiological examinations and 650,000 individual laboratory measurements. Integration of routine electronic health care in aresearch data platform allows efficient data collection, including all investigations in chronological sequence. Trials embedded in the electronic health record are now possible, providing cost-effective ways to answer clinical questions. We explicitly welcome national and international collaboration and have provided our protocols and other materials on www.unravelrdp.nl .
机译:尽管我们对遗传心肌病的理解有重大进展,但它们仍然是60岁以下的早熟心脏死亡和终末期心力衰竭的主要原因。基于Alarge数量的患者的综合研究数据库可能会提供亚替代的研究。使用常规电子健康记录和标准化的生物库,可能的临时患者数量和调查的大数据分析。在本文中,我们描述了嵌入在常规实践中的UnRapl研究数据平台,以促进遗传心脏病的研究。符合条件的参与者有经过验证或疑似的心脏病和他们的亲属,允许使用他们的数据并吸引生物库的血液。经常收集的临床数据通过每周提取中包含在研究数据库中。已经开发了Atext-Mining工具,以在临床笔记中使用非结构化数据进行丰富的衰退。到目前为止,已包括828名以57年为57年的人,其中58%是男性。所有数据都捕获以18,565个心电图,3619公仔,来自超过20,000多个放射检查的数据和650,000个单个实验室测量的数据。在Aresearch数据平台中常规电子医疗保健的集成允许高效的数据收集,包括按时间顺序排序的所有调查。现在可以提供嵌入电子健康记录中的试验,为应对临床问题提供具有成本效益的方法。我们明确欢迎国家和国际合作,并在www.unravelrdp.nl上提供了我们的协议和其他材料。
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