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Design and Testing of an EHR-Integrated, Busulfan Pharmacokinetic Decision Support Tool for the Point-of-Care Clinician

机译:面向现场护理人员的EHR集成,白消安药代动力学决策支持工具的设计和测试

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Background: Busulfan demonstrates a narrow therapeutic index for which clinicians routinely employ therapeutic drug monitoring (TDM). However, operationalizing TDM can be fraught with inefficiency. We developed and tested software encoding a clinical decision support tool (DST) that is embedded into our electronic health record (EHR) and designed to streamline the TDM process for our oncology partners. Methods: Our development strategy was modeled based on the features associated with successful DSTs. An initial Requirements Analysis was performed to characterize tasks, information flow, user needs, and system requirements to enable push/pull from the EHR. Back-end development was coded based on the algorithm used when manually performing busulfan TDM. The code was independently validated in MATLAB using 10,000 simulated patient profiles. A 296-item heuristic checklist was used to guide design of the front-end user interface. Content experts and end-users ( n = 28) were recruited to participate in traditional usability testing under an IRB approved protocol. Results: Decision support software was developed to systematically walk the point-of-care clinician through the TDM process. The system is accessed through the EHR which transparently imports all of the requisite patient data. Data are visually inspected and then curve fit using a model-dependent approach. Quantitative goodness-of-fit are converted to single tachometer where “green” alerts the user that the model is strong, “yellow” signals caution and “red” indicates that there may be a problem with the fitting. Override features are embedded to permit application of a model-independent approach where appropriate. Simulations are performed to target a desired exposure or dose as entered by the clinician and the DST pushes the user approved recommendation back into the EHR. Usability testers were highly satisfied with our DST and quickly became proficient with the software. Conclusions: With early and broad stake-holder engagement we developed a clinical DST for the non-pharmacologist. This tools affords our clinicians the ability to seamlessly transition from patient assessment, to pharmacokinetic modeling and simulation, and subsequent prescription order entry.
机译:背景:白消安证明了较窄的治疗指数,临床医生对此常规采用治疗药物监测(TDM)。但是,运营TDM可能会效率低下。我们开发并测试了编码临床决策支持工具(DST)的软件,该软件已嵌入到我们的电子健康记录(EHR)中,旨在为我们的肿瘤学合作伙伴简化TDM流程。方法:我们基于与成功的DST相关的功能对开发策略进行了建模。进行了初始需求分析,以表征任务,信息流,用户需求和系统需求,以实现从EHR进行推/拉。后端开发是根据手动执行白消安TDM时使用的算法进行编码的。该代码已在MATLAB中使用10,000个模拟患者资料进行了独立验证。 296个项目的启发式检查表用于指导前端用户界面的设计。根据IRB批准的协议,内容专家和最终用户(n = 28)被招募参加传统的可用性测试。结果:开发了决策支持软件,以系统地指导医疗点临床医生完成TDM流程。通过EHR访问该系统,该EHR透明地导入所有必需的患者数据。目视检查数据,然后使用依赖于模型的方法进行曲线拟合。定量拟合优度转换为单个转速表,其中“绿色”警告用户该模型很坚固,“黄色”表示警告,而“红色”表示该拟合可能存在问题。嵌入了替代功能,以允许在适当的情况下应用与模型无关的方法。进行模拟以针对临床医生输入的所需暴露量或剂量,DST将用户批准的推荐推回EHR。可用性测试人员对我们的DST非常满意,并很快精通该软件。结论:在早期和广泛的利益相关者参与下,我们为非药物学家开发了临床DST。该工具使我们的临床医生能够无缝地从患者评估过渡到药代动力学建模和模拟,以及随后的处方单输入。

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