Kane-Gill Sandra L, Achanta Archita, Kellum John A, Handler Steven M
Sandra L Kane-Gill, Department of Pharmacy and Therapeutics, School of Pharmacy, University of Pittsburgh, Pittsburgh, PA 15261, United States.
World J Crit Care Med. 2016 Nov 4;5(4):204-211. doi: 10.5492/wjccm.v5.i4.204.
Clinical decision support (CDS) systems with automated alerts integrated into electronic medical records demonstrate efficacy for detecting medication errors (ME) and adverse drug events (ADEs). Critically ill patients are at increased risk for ME, ADEs and serious negative outcomes related to these events. Capitalizing on CDS to detect ME and prevent adverse drug related events has the potential to improve patient outcomes. The key to an effective medication safety surveillance system incorporating CDS is advancing the signals for alerts by using trajectory analyses to predict clinical events, instead of waiting for these events to occur. Additionally, incorporating cutting-edge biomarkers into alert knowledge in an effort to identify the need to adjust medication therapy portending harm will advance the current state of CDS. CDS can be taken a step further to identify drug related physiological events, which are less commonly included in surveillance systems. Predictive models for adverse events that combine patient factors with laboratory values and biomarkers are being established and these models can be the foundation for individualized CDS alerts to prevent impending ADEs.
集成到电子病历中的带有自动警报功能的临床决策支持(CDS)系统已证明在检测用药错误(ME)和药物不良事件(ADE)方面具有功效。重症患者发生ME、ADE以及与这些事件相关的严重负面结果的风险增加。利用CDS来检测ME并预防药物相关不良事件有可能改善患者预后。一个有效的包含CDS的用药安全监测系统的关键在于,通过使用轨迹分析来预测临床事件,而不是等待这些事件发生,从而推进警报信号。此外,将前沿生物标志物纳入警报知识中,以识别调整可能造成伤害的药物治疗的必要性,这将推动CDS的现状发展。CDS可以进一步发展以识别与药物相关的生理事件,而这些事件在监测系统中较少被纳入。结合患者因素、实验室值和生物标志物的不良事件预测模型正在建立,这些模型可以成为个性化CDS警报的基础,以预防即将发生的ADE。