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使用IHE高级患者隐私同意书实施模块化研究同意书。

Implementing Modular Research Consents Using IHE Advanced Patient Privacy Consents.

作者信息

Schreiweis Bjoern, Bronsch Tobias, Merzweiler Angela, Bergh Bjoern

机构信息

Department of Medical Information Systems, University Hospital Heidelberg, Germany.

出版信息

Stud Health Technol Inform. 2018;247:840-844.

Abstract

The re-use of healthcare information for biomedical research is increasing and with it the importance of a consent management framework implementing computable consents. Based on requirements concerning a consent representation the Advanced Patient Privacy Consents (APPC) Profile of Integrating the Healthcare Enterprise (IHE) is evaluated and mapped to these requirements. As IHE APPC was developed for computable patient consents, the mapping of consents for research projects is possible by re-using the elements defined. Compared to other approaches like gICS, approaches using APPC can be based on commercial software products and integrated into IHE environments. IHE APPC was already successfully used in EHR projects like INFOPAT. For interoperability reasons IT platforms intending to support biomedical research including clinical data, research data, biomaterial and imaging data, IHE APPC seems to be an appropriate standard to choose.

摘要

医疗保健信息在生物医学研究中的再利用正在增加,随之而来的是实施可计算同意书的同意管理框架的重要性。基于有关同意书表示的要求,对整合医疗企业(IHE)的高级患者隐私同意书(APPC)概要文件进行评估并将其映射到这些要求。由于IHE APPC是为可计算的患者同意书而开发的,因此通过重新使用已定义的元素,可以对研究项目的同意书进行映射。与其他方法(如gICS)相比,使用APPC的方法可以基于商业软件产品并集成到IHE环境中。IHE APPC已经在诸如INFOPAT等电子健康记录项目中成功使用。出于互操作性的原因,对于打算支持包括临床数据、研究数据、生物材料和成像数据在内的生物医学研究的IT平台,IHE APPC似乎是一个合适的选择标准。

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