分析电子病历系统中用于抗凝管理的临床记录数据。

T Austin, D Kalra, N C Lea, D L H Patterson, D Ingram
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目的:本文报告了对通用电子健康记录信息模型属性的评估:本文报告了对通用电子健康记录信息模型属性的评估,这些属性是在将现有临床应用程序导入通用电子健康记录存储库时实际需要和使用的:方法:作为欧盟项目 Synapses 和 SynEx 的一部分,开发了通用电子病历库和系统。开发了一个支持抗凝疗法管理的网络应用程序,与电子病历系统相连接,并在伦敦北部的一家医院内部署,其中包含了之前现有抗凝管理应用程序中累积的五年临床数据。这提供了一个机会,可以对通用电子病历中实际需要用来表示遗留数据的部分进行批判:导入了 3,226 名患者的抗凝记录,并使用超过 900,000 个记录组件(即每名患者的记录平均包含 289 个节点)来表示,其中约三分之二为元素项(即含数值的叶节点),其余为容器节点(即标题和副标题)。每个节点都能包含丰富的上下文属性,但在现实中,我们发现许多属性根本没有被使用过,有些甚至很少被使用(例如,只有约 0.5% 的记录组件被修改过):结论:开发通用电子病历信息模型的过程主要是由需求驱动的,这些需求来自研究,并体现在新一代互操作性标准和规范中。这些需求主要是通过从临床社区收集用例和实例收集而来,并被添加到这些模型的历代版本中。迄今为止,我们还没有采用确定优先级的方法--所有的要求都已收到,而且几乎无一例外地得到了满足。这项工作表明,所产生的模型实际上只需要很少的内容就能代表有用和可用的临床数据。为了平衡理论上的需求收集过程,需要对不同类型的现有临床系统进行更广泛的此类评估,以产生具有理想复杂程度的电子病历信息模型。
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Analysis of Clinical Record Data for Anticoagulation Management within an EHR System.

Objectives: This paper reports an evaluation of the properties of a generic electronic health record information model that were actually required and used when importing an existing clinical application into a generic EHR repository.

Method: A generic EHR repository and system were developed as part of the EU Projects Synapses and SynEx. A Web application to support the management of anticoagulation therapy was developed to interface to the EHR system, and deployed within a north London hospital with five years of cumulative clinical data from the previous existing anticoagulation management application. This offered the opportunity to critique those parts of the generic EHR that were actually needed to represent the legacy data.

Results: The anticoagulation records from 3,226 patients were imported and represented using over 900,000 Record Components (i.e. each patient's record contained on average 289 nodes), of which around two thirds were Element Items (i.e. value-containing leaf nodes), the remainder being container nodes (i.e. headings and sub-headings). Each node is capable of incorporating a rich set of context properties, but in reality it was found that many properties were not used at all, and some infrequently (e.g. only around 0.5% of Record Components had ever been revised).

Conclusions: The process of developing generic EHR information models, arising from research and embodied within new-generation interoperability standards and specifications, has been strongly driven by requirements. These requirements have been gathered primarily by collecting use cases and examples from clinical communities, and been added to successive generations of these models. A priority setting approach has not to date been pursued - all requirements have been received and almost invariably met. This work has shown how little of the resulting model is actually needed to represent useful and usable clinical data. A wider range of such evaluations, looking at different kinds of existing clinical system, is needed to balance the theoretical requirements gathering processes, in order to result in EHR information models of an ideal level of complexity.

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