药物安全监督中的交互式仪表板的设计原则:设计科学研究
Malwina Kotowicz1, Mexhid Ferati1, Soumitra Chowdhury1
1Department of Informatics, Faculty of Technology, Linnaeus University, Växjö, 351 95, Sweden, 46 470767999.
JMIR medical informatics
|March 3, 2026
概括
这项研究开发了药物安全仪表板的设计原则,增强了以用户为中心的设计,以改善药物监督和决策. 由此产生的原型实现了84%的可用性,改善了药物安全数据的理解.
科学领域:
- 医疗信息学 医疗信息学
- 人与计算机的交互
- 药物监督 药物监督 药物监督
背景情况:
- 药物不良反应 (ADRs) 带来了重大的健康风险和经济负担.
- 药物安全监测仪表板是缓解这些风险的关键工具.
研究的目的:
- 开发一个以用户为中心的药物安全跟踪仪表板.
- 通过负担能力理论和最终用户参与,制定和完善药物安全仪表板的设计原则 (DP).
主要方法:
- 一种设计科学研究方法,有3个代的设计和评估周期.
- 4名专业和6名非专业的最终用户参与了共同设计研讨会,可用性测试和启发性评估.
主要成果:
- 一套基于负担能力理论的8个精细的DP,指导立即使用的仪表板设计,模式识别,趋势跟踪,用户控制和决策支持.
- 一个高保真仪表板原型实现了84%的整体可用性得分.
结论:
- 基于负担能力理论的DP产生了与用户相关的文物,用于改善药物安全数据的理解和决策.
- 在开发药物监督仪表板方面证明了负担能力的实用性.
- 这些发现可能适用于类似的健康信息系统.
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