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How safe is information about medicines? A risk assessment framework

机译:有关药物的信息有多安全?风险评估框架

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Purpose - The purpose of this paper is to identify factors predisposing to risk in publications written by healthcare professionals, especially those concerned with medicines. Design/methodology/approach - Observation, discussion, and analysis of production methods, standards, and written outputs produced by the UK Medicines Information network as an exemplar of a healthcare organisation producing an array of publications with an accompanying tier of pre-publication quality assurance procedures. Findings - The factors which affect the likelihood and impact of risk in publications can be identified: author competence, quality of information sources, transformation process, audience, provenance, intended use and subject matter. These factors can be used to score a given publication and establish its risk potential relative to other publications. Practical implications - It is recommended that healthcare organisations engaged in producing written material consider carefully the risks inherent in publishing, and the factors which influence risk. Originality/value - The factors identified here can be used to score relative risk and to identify the highest risk publications. Higher risk documents should attract the most stringent pre-publication quality assurance procedures.
机译:目的-本文的目的是确定由医疗保健专业人员(尤其是与药物相关的专业人员)撰写的出版物中容易引发风险的因素。设计/方法/方法-观察,讨论和分析生产方法,标准和英国药品信息网提供的书面输出,作为医疗机构的范例,该机构生产一系列出版物以及附带的出版前质量保证体系程序。调查结果-可以确定影响出版物中风险可能性和影响的因素:作者能力,信息源质量,转换过程,受众,出处,预期用途和主题。这些因素可用于对给定出版物进行评分并确定其相对于其他出版物的潜在风险。实际意义-建议从事书面材料制作的医疗机构仔细考虑出版固有的风险以及影响风险的因素。原创性/价值-此处确定的因素可用于对相对风险进行评分并确定最高风险的出版物。高风险文件应吸引最严格的出版前质量保证程序。

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