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Utilizing a user-centered approach to develop and assess pharmacogenomic clinical decision support for thiopurine methyltransferase

机译:利用以用户为中心的方法开发和评估硫代嘌呤甲基转移酶的药物基因组学临床决策支持

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A pharmacogenomic clinical decision support tool (PGx-CDS) for thiopurine medications can help physicians incorporate pharmacogenomic results into prescribing decisions by providing up-to-date, real-time decision support. However, the PGx-CDS user interface may introduce errors and promote alert fatigue. The objective of this study was to develop and evaluate a prototype of a PGx-CDS user interface for thiopurine medications with user-centered design methods. This study had two phases: In phase I, we conducted qualitative interviews to assess providers’ information needs. Interview transcripts were analyzed through a combination of inductive and deductive qualitative analysis to develop design requirements for a PGx-CDS user interface. Using these requirements, we developed a user interface prototype and evaluated its usability (phase II). In total, 14 providers participated: 10 were interviewed in phase I, and seven providers completed usability testing in phase II (3 providers participated in both phases). Most (90%) participants were interested in PGx-CDS systems to help improve medication efficacy and patient safety. Interviews yielded 11 themes sorted into two main categories: 1) health care providers’ views on PGx-CDS and 2) important design features for PGx-CDS. We organized these findings into guidance for PGx-CDS content and display. Usability testing of the PGx-CDS prototype showed high provider satisfaction. This is one of the first studies to utilize a user-centered design approach to develop and assess a PGx-CDS interface prototype for Thiopurine Methyltransferase (TPMT). This study provides guidance for the development of a PGx-CDS, and particularly for biomarkers such as TPMT.
机译:用于硫嘌呤药物的药物基因组学临床决策支持工具(PGx-CDS)可通过提供最新的实时决策支持,帮助医生将药物基因组学结果纳入处方决策中。但是,PGx-CDS用户界面可能会引入错误并加剧警报疲劳。这项研究的目的是使用以用户为中心的设计方法,开发和评估用于硫嘌呤药物的PGx-CDS用户界面的原型。这项研究分为两个阶段:在第一阶段,我们进行了定性访谈,以评估提供者的信息需求。通过归纳和演绎定性分析相结合的方式对访谈记录进行了分析,以制定PGx-CDS用户界面的设计要求。根据这些要求,我们开发了用户界面原型并评估了其可用性(阶段II)。总共有14家提供商参与其中:第一阶段采访了10名提供商,第二阶段有7家提供商完成了可用性测试(两个阶段中都有3家提供商参与了测试)。大多数(90%)参与者对PGx-CDS系统感兴趣,以帮助改善药物疗效和患者安全。访谈产生了11个主题,分为两个主要类别:1)医疗保健提供者对PGx-CDS的看法,以及2)PGx-CDS的重要设计功能。我们将这些发现整理为PGx-CDS内容和显示的指南。 PGx-CDS原型的可用性测试显示出较高的提供商满意度。这是利用用户中心设计方法开发和评估硫嘌呤甲基转移酶(TPMT)的PGx-CDS接口原型的首批研究之一。这项研究为PGx-CDS的开发提供了指导,特别是对于TPMT等生物标志物。

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