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An Approach to 'Dynamic - DDD (Defined Daily Dose) Monitoring' to Reduce Adverse Clinical Outcomes and Increase Patient Safety: Information Repositories and Event Triggers in Clinical Practice

机译:一种“动态 - DDD(定义的每日剂量)监测”的方法,以减少不良临床结果,增加患者安全:临床实践中的信息储存库和事件触发

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The goal of every effort and actions/interventions in almost all healthcare settings throughout the world's health systems -primary care, inpatient, outpatient encounters, diagnostic and therapeutic interventions, peri-operative settings- is and has been to achieve a well defined outcome (a kind of improvement in health status of the patient under consideration, an observable and significant change(s) in selected set(s) of clinical parameters confirmed by laboratory results and pathology findings, improvements in clinical outcomes). Clinical inefficiencies, in this context, should be addressed very systematically and scientifically. This is achieved through a continuously monitoring approach to adverse drug events based on information repositories and evidence-based rule sets. For monitoring drug-related outcomes and clinical outcomes in general, the concept of DDD (Defined Daily Dose) compliance is explained in this article to eliminate and avoid adverse clinical outcomes.
机译:几乎所有努力和行动/干预的目标,几乎所有医疗保健系统的卫生系统 - 关注,住院患者,门诊遭遇,诊断和治疗干预,诊断和治疗干预措施,都是达到明确的结果(a通过实验室结果和病理结果证实的临床参数的所选组中患者健康状况的改善,可观察和显着的变化,通过实验室结果和病理结果证实,临床结果的改进)。在这种情况下,临床效率低效率应该非常有系统和科学地解决。这是通过基于信息存储库和基于证据的规则集的不断监测不良药物事件的不断监测方法来实现。对于监测药物相关的结果和临床结果,通常在本文中解释了DDD(定义的每日剂量)合规性的概念,以消除并避免不良临床结果。

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