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Registries of implantable medical devices in Europe

机译:欧洲植入式医疗设备注册

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摘要

Background: In early 2012, a number of serious events in the implant area raised public awareness and started a discussion on safety issues and monitoring medical devices in academics and politics. Apparently, there is a lack in the surveillance of medical devices. Therefore, the objective of this work is to detect and classify implant registries in Europe. Methods and findings: A systematic search of literature was carried out to identify the different types of registries. Furthermore, to characterize the implant registries by different criteria a medical device classification system was established. One hundred and one European registries were found. Most registries exist in the field of cardiac implants and arthroplasty (38 and 29) and their distribution showed variation within Europe. For a lot of implant categories, none or very few registries could be identified. Some countries run more registries than others. There are a lot of differences in aim and structure among the registries. Conclusion: There is only a limited number of reviews on registries and a centralized monitoring system in Europe is missing. Our results reveal a lack of transparency concerning number, aim, structure and quality of registries. This is crucial, as registries work as early warning systems for identifying and notifying patients at risk.
机译:背景:2012年初,植入物领域发生了一系列严重事件,提高了公众的意识,并开始就安全问题以及学术界和政治界对医疗器械的监控进行讨论。显然,缺乏对医疗设备的监视。因此,这项工作的目的是对欧洲的植入物注册进行检测和分类。方法和调查结果:对文献进行了系统的搜索,以确定不同类型的注册机构。此外,为了通过不同标准表征植入物登记处,建立了医疗设备分类系统。找到了一百零一个欧洲注册表。大多数登记册存在于心脏植入物和人工关节成形术领域(38和29),其分布在欧洲范围内有所不同。对于很多植入物类别,没有或只有很少的注册表可以被识别。一些国家/地区比其他国家/地区拥有更多的注册管理机构。各注册管理机构的目标和结构存在很多差异。结论:注册管理机构的审查数量有限,欧洲缺少集中监控系统。我们的结果表明,注册管理机构的数量,目标,结构和质量缺乏透明度。这一点至关重要,因为注册管理机构可以作为预警系统来识别和通知处于危险之中的患者。

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