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Analysis of requirements for the medication profile to be used in clinical research : protocol feasibility studies and patient recruitment

机译:分析用于临床研究的药物概况的要求:方案可行性研究和患者招募

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摘要

A "Medication Profile," the information about the medicines a person is using and has used, is a core part of many electronic health record systems and summaries. However, there is little objective research into the data elements that the profile should contain to support the uses it must serve. With the increasing emphasis on secondary uses of electronic health information, as well as supporting the requirements to support direct to patient care, the Medication Profile should also support the requirements from clinical research. However, there is little, if any, description of these available. This paper describes an analysis of a set of study eligibility criteria that was undertaken to investigate which medication-related data elements would be required to support two clinical research use cases: the parameters to query a patient's Medication Profile to assess their suitability for entry into a trial (patient recruitment) and the parameters to query a set of Medication Profiles in a data warehouse to assess whether the eligibility criteria as described would yield a reasonable cohort of patients as potential subjects (protocol feasibility). These medication-related data elements then become information requirements that a Medication Profile should ideally meet, in order to be able to support these two uses in the clinical research domain.
机译:“药物档案”是一个人正在使用和已经使用的药物的信息,是许多电子健康记录系统和摘要的核心部分。但是,对于概要文件应包含的数据元素以支持其必须服务的用途,几乎没有客观的研究。随着越来越重视电子健康信息的二次使用以及支持直接支持患者护理的要求,药物概况也应支持临床研究的要求。但是,几乎没有可用的描述。本文描述了对一组研究资格标准的分析,该标准旨在调查支持两个临床研究用例需要哪些与药物相关的数据元素:查询患者药物概况以评估其是否适合入药的参数试验(患者招募)以及在数据仓库中查询一组用药档案以评估所描述的资格标准是否可以使合理的患者群体作为潜在受试者的参数(协议可行性)。然后,这些与药物有关的数据元素成为“药物档案”理想地应满足的信息要求,以便能够在临床研究领域中支持这两种用途。

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