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用于监测药物相互作用和增加钾的药物组合的临床决策支持:对特定警报的需求。

Clinical decision support for monitoring drug-drug-interactions and potassium-increasing drug combinations: need for specific alerts.

作者信息

Eschmann Emmanuel, Beeler Patrick E, Kaplan Vladimir, Schneemann Markus, Zünd Gregor, Blaser Jürg

机构信息

Research Centre for Medical Informatics, University Hospital, Zurich, Switzerland.

出版信息

Stud Health Technol Inform. 2012;180:1200-2.

Abstract

Computer-triggered reminders alerting physicians on every potentially harmful drug-drug-interaction (DDI) induce alert fatigue due to frequent messages of limited clinical relevance. On demand DDI-checks, however, are not commonly used by physicians. Optimal strategies for sustained quality assurance have to consider patients' risk factors and focus on the most significant DDIs only. An approach is proposed based on the analysis of concurrent prescription of potassium-sparing diuretics and potassium supplements (CPPP), which are the most frequent DDIs classified as contraindicated. Although the frequency of monitoring potassium serum levels declined during prolonged periods of CPPP, the likelihood of observing a hyperkalaemia increased. The median treatment period of CPPP was 3.3 days, whereas hyperkalaemia occurred after a median observation time of 4.5 days of CPPP. Thus, computer-triggered reminders for ordering potassium serum levels may be indicated if monitoring has been discontinued after 48h of CPPP.

摘要

计算机触发的提醒会就每一种潜在有害的药物相互作用(DDI)向医生发出警报,由于频繁发送临床相关性有限的信息,会导致警报疲劳。然而,按需进行的药物相互作用检查医生并不常用。持续质量保证的最佳策略必须考虑患者的风险因素,并且仅关注最重要的药物相互作用。本文提出了一种基于对保钾利尿剂和钾补充剂同时处方(CPPP)分析的方法,这是最常见的被列为禁忌的药物相互作用。尽管在长期的CPPP期间监测血清钾水平的频率有所下降,但出现高钾血症的可能性增加了。CPPP的中位治疗期为3.3天,而高钾血症在CPPP的中位观察时间4.5天后出现。因此,如果在CPPP 48小时后停止监测,可能需要计算机触发提醒来安排血清钾水平检测。

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