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预防用药差错国际培训班(西宁)最新培训议程

来源:www.29977.com原创    发布时间:2011-06-08

Learning Objectives: After attending this workshop, participants will be ableto:

学习目标:通过本次研讨会,与会者将能够

? Understand key medication error terminology including types, causes and the differences between a medicationerror, adverse drug reaction and adverse drug event

了解用药差错术语(类型、原因)及用药差错、不良反应和药物不良事件之间的差异

?Categorize the severity of a medication error using a standardized indexing tool developed by a panel of patient safety experts

通过利用患者安全专家平台开发出的标准索引工具,对用药差错的严重程度进行分类。

?Describe a variety of methods that can be used to identify medication safety risks within a hospital or other healthcare facilities

描述能够在医院或其他医疗机构中鉴别药物安全风险的几种方法

?Use proven safety tools to investigate system-based causes of error and reach conclusions on the actions that should be taken that result from successful error analysis

使用经证明有效的安全工具调查用药差错的系统性原因,并通过成功的差错分析,采取措施从而找到结论。

?Set priorities for risk-reduction strategies and learn the strength levels of these different strategies

建立降低风险策略的优先次序,学习这些不同策略的优势水平。

Program Agenda – Day 1议程-第一天7.23)

?Error Terminology and Categorization  用药差错术语和分类

o  Differentiate between errors and other types of adverse drug events

用药差错与其他类型药物不良事件间的差异

o  Understand the basic framework for categorizing errors by severity, type, and cause

理解根据严重程度、类型和原因分类用药差错的基本框架

o  Case Studies: use real error cases to practice using a standardized indexing tool

案例研究:通过真实的用药差错案例练习使用标准索引工具

?Risk Analysis: Individual Report Analysis  风险分析:个别报告分析

o  Learn to examine error events from a system-based perspective rather than blaming individuals

学习从系统化的角度审视用药差错事件而不是归咎于个别事件

o  Learn the 10 key safety elements that provide the foundation for in-depth examination of the potential medication system weaknesses 

学会关于深入检验潜在的药品系统弱点的10个重要安全要素

o  Understand the role of latent failures and active failures to better understand how errors occur

了解隐性失效和显性失效,以便更好地理解用药差错是如何发生的

o  Case Studies: use an individual error event to examine and analyze the 10 key safety elements

案例研究:通过个别用药差错事件检验并分析10个重要安全要素

?Discussion / Question and Answer Session讨论/问答环节

 

Program Agenda – Day 2议程-第二天(7.24)

?Risk Identification Part I: Medication Error Reporting Programs

风险识别 I:用药差错报告程序

o  Understand the various data collection methods for spontaneous reporting of error events

了解收集用药差错事件自发报告数据的多种方法

o  Learn the advantages and disadvantages of reporting programs

学习报告程序的优缺点

?Risk Identification Part II: Identifying Risk Beyond Reporting Programs

风险识别 II:识别风险重于报告程序

o  Learn proven safety tools to proactively, concurrently, and retrospectively assess risk 

学习利用已被证明安全的工具前摄性地、并发性地及回顾性地对风险进行评估。

? Risk Analysis: Evaluating Aggregate Data  风险分析:评估综合资料

o  Learn to transform aggregate error data into meaningful information and display results in tables and charts

学习将综合用药差错数据转换为有意义的信息并在图表中显示结果

o  Breakout Session – workgroups to review aggregate medication error data from a US hospital and answer a series of questions.

分组讨论-小组讨论某美国医院的综合用药差错数据,回答一系列问题

?Risk Control: Choosing Effective Error Reduction Strategies

风险控制:选择有效减少用药差错的策略

o  Explain the goals and principles of medication error prevention and harm reduction, and learn the difference between high and low leverage strategies

说明预防用药差错和减少损害的目标和原则,学习不同层次策略的差异

?Examining Interventions: Assessing Impact of Error Reduction Strategies

检验干预:评估减少用药差错策略带来的影响

o  Learn which questions about developing an action plan, weighting of actions, and first and second order changes

学习创立一项活动计划、衡量活动质量和第一第二层次将涉及的问题

Discussion / Question and Answer Session  讨论/问答环节

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