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首页> 外文期刊>BMC Medical Informatics and Decision Making >How to promote adverse drug reaction reports using information systems – a systematic review and meta-analysis
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How to promote adverse drug reaction reports using information systems – a systematic review and meta-analysis

机译:如何使用信息系统促进药物不良反应报告的系统评价和荟萃分析

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Background Adverse drug reactions (ADRs) are a well-recognized public health problem and a major cause of death and hospitalization in developed countries. The safety of a new drug cannot be established until it has been on the market for several years. Keeping drug reactions under surveillance through pharmacovigilance systems is indispensable. However, underreporting is a major issue that undermines the effectiveness of spontaneous reports. Our work presents a systematic review on the use of information systems for the promotion of ADR reporting. The aim of this work is to describe the state of the art information systems used to promote adverse drug reaction reporting. Methods A systematic review was performed with quantitative analysis of studies describing or evaluating the use of information systems to promote adverse drug reaction reporting. Studies with data related to the number of ADRs reported before and after each intervention and the follow-up period were included in the quantitative analysis. Results From a total of 3865 articles, 33 articles were included in the analysis; these articles described 29 different projects. Most of the projects were on a regional scale (62?%) and were performed in a hospital context (52?%). A total of 76?% performed passive promotion of ADR reporting and used web-based software (55?%). A total of 72?% targeted healthcare professionals and 24?% were oriented to patient ADR reporting. We performed a meta-analysis of 7 of the 29 projects to calculate the aggregated measure of the ADR reporting increase, which had an overall measure of 2.1 (indicating that the interventions doubled the number of ADRs reported). Conclusions We found that most of the projects performed passive promotion of ADR reporting (i.e., facilitating the process). They were developed in hospitals and were tailored to healthcare professionals. These interventions doubled the number of ADR reports. We believe that it would be useful to develop systems to assist healthcare professionals with completing ADR reporting within electronic health records because this approach seems to be an efficient method to increase the ADR reporting rate. When this approach is not possible, it is essential to have a tool that is easily accessible on the web to report ADRs. This tool can be promoted by sending emails or through the inclusion of direct hyperlinks on healthcare professionals’ desktops.
机译:背景技术药物不良反应(ADR)是公认的公共卫生问题,在发达国家是导致死亡和住院的主要原因。在新药上市几年之前,其安全性无法确立。通过药物警戒系统对药物反应进行监视是必不可少的。但是,漏报是一个主要问题,破坏了自发报告的有效性。我们的工作对使用信息系统促进ADR报告的系统化进行了回顾。这项工作的目的是描述用于促进不良药物反应报告的最新信息系统。方法对描述或评估信息系统以促进不良药物反应报告的研究进行定量分析,进行系统的评价。定量分析中包括与每次干预前后报告的ADR数量相关的数据以及随访期的研究。结果共纳入3865篇文章,其中33篇纳入分析。这些文章描述了29个不同的项目。大多数项目在区域范围内(占62%),是在医院范围内进行的(占52%)。共有76%的人进行了ADR报告的被动推广并使用了基于Web的软件(占55%)。共有72%的目标医疗专业人员和24%的患者针对患者的ADR报告。我们对29个项目中的7个进行了荟萃分析,以计算ADR报告增幅的汇总量度,总体评估值为2.1(表明干预措施使报告的ADR数量增加了一倍)。结论我们发现,大多数项目执行了ADR报告的被动推广(即,促进了流程)。它们是在医院开发的,专门针对医疗保健专业人员。这些干预使ADR报告的数量增加了一倍。我们认为,开发有助于医疗保健专业人员在电子健康记录中完成ADR报告的系统将很有用,因为这种方法似乎是提高ADR报告率的有效方法。如果无法采用这种方法,则必须拥有一个可在Web上轻松访问以报告ADR的工具。可以通过发送电子邮件或在医疗保健专业人员的桌面上包含直接超链接来推广此工具。

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