Second generation registry framework.

Q2 Decision Sciences
Source Code for Biology and Medicine Pub Date : 2014-06-20 eCollection Date: 2014-01-01 DOI:10.1186/1751-0473-9-14
Matthew I Bellgard, Lee Render, Maciej Radochonski, Adam Hunter
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引用次数: 25

Abstract

Background: Information management systems are essential to capture data be it for public health and human disease, sustainable agriculture, or plant and animal biosecurity. In public health, the term patient registry is often used to describe information management systems that are used to record and track phenotypic data of patients. Appropriate design, implementation and deployment of patient registries enables rapid decision making and ongoing data mining ultimately leading to improved patient outcomes. A major bottleneck encountered is the static nature of these registries. That is, software developers are required to work with stakeholders to determine requirements, design the system, implement the required data fields and functionality for each patient registry. Additionally, software developer time is required for ongoing maintenance and customisation. It is desirable to deploy a sophisticated registry framework that can allow scientists and registry curators possessing standard computing skills to dynamically construct a complete patient registry from scratch and customise it for their specific needs with little or no need to engage a software developer at any stage.

Results: This paper introduces our second generation open source registry framework which builds on our previous rare disease registry framework (RDRF). This second generation RDRF is a new approach as it empowers registry administrators to construct one or more patient registries without software developer effort. New data elements for a diverse range of phenotypic and genotypic measurements can be defined at any time. Defined data elements can then be utilised in any of the created registries. Fine grained, multi-level user and workgroup access can be applied to each data element to ensure appropriate access and data privacy. We introduce the concept of derived data elements to assist the data element standards communities on how they might be best categorised.

Conclusions: We introduce the second generation RDRF that enables the user-driven dynamic creation of patient registries. We believe this second generation RDRF is a novel approach to patient registry design, implementation and deployment and a significant advance on existing registry systems.

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第二代注册表框架。
背景:信息管理系统对于获取有关公共卫生和人类疾病、可持续农业或动植物生物安全的数据至关重要。在公共卫生领域,术语“患者登记”通常用于描述用于记录和跟踪患者表型数据的信息管理系统。患者注册的适当设计、实施和部署可以实现快速决策和持续的数据挖掘,最终改善患者的治疗效果。遇到的一个主要瓶颈是这些注册中心的静态特性。也就是说,软件开发人员需要与利益相关者一起确定需求、设计系统、实现每个患者登记处所需的数据字段和功能。此外,软件开发人员需要时间进行持续的维护和定制。我们希望部署一个复杂的注册表框架,使拥有标准计算技能的科学家和注册表管理员能够从头开始动态地构建一个完整的患者注册表,并根据他们的具体需求进行定制,而在任何阶段都很少或根本不需要聘请软件开发人员。结果:本文介绍了我们的第二代开源注册框架,它建立在我们之前的罕见病注册框架(RDRF)的基础上。第二代RDRF是一种新方法,因为它使注册中心管理员能够构建一个或多个患者注册中心,而无需软件开发人员的努力。可以在任何时候定义各种表型和基因型测量的新数据元素。然后可以在任何创建的注册中心中使用定义的数据元素。细粒度、多层次的用户和工作组访问可以应用于每个数据元素,以确保适当的访问和数据隐私。我们引入了派生数据元素的概念,以帮助数据元素标准团体了解如何对它们进行最佳分类。结论:我们介绍了第二代RDRF,它支持用户驱动的患者注册动态创建。我们相信,第二代RDRF是患者登记设计、实施和部署的新方法,是现有登记系统的重大进步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Source Code for Biology and Medicine
Source Code for Biology and Medicine Decision Sciences-Information Systems and Management
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期刊介绍: Source Code for Biology and Medicine is a peer-reviewed open access, online journal that publishes articles on source code employed over a wide range of applications in biology and medicine. The journal"s aim is to publish source code for distribution and use in the public domain in order to advance biological and medical research. Through this dissemination, it may be possible to shorten the time required for solving certain computational problems for which there is limited source code availability or resources.
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