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Postmarketing surveillance in Brazil: vascular catheters ?¢???? an overview of notifications of adverse events and technical complaints

机译:巴西的上市后监视:血管导管不良事件和技术投诉通知的概述

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Abstract This article identifies, quantifies and categorizes adverse event notifications and technical complaints related to the use of vascular catheters, received by the Notivisa system in the period from January 2007 to June 2016. It is a descriptive, retrospective, documental study with a quantitative approach. Data requested and supplied by Anvisa were analyzed and presented in the form of charts and tables. The study covered 4,682 notifications of technical complaints, and 671 adverse events. There was a progressive increase in notifications during the period studied. As to the type of technical complaint, the majority referred to ?¢????suspected quality failings?¢????, the largest component being due to ?¢????catheter rupture during procedure?¢????. The adverse event most notified was ?¢????catheter broke in the vein and migrated to another part of the body?¢????. In the period studied there were four notifications of deaths, the most severe level of adverse event. The study made it possible to visualize the importance of after-sales surveillance of vascular catheters, as well as supplying a wide-ranging overview of their use. Provision of this overview could support technical surveillance activities and serve as input for public policies relating to this product.
机译:摘要本文对2007年1月至2016年6月期间Notivisa系统收到的与使用血管导管有关的不良事件通知和技术投诉进行了识别,量化和分类。 。对Anvisa要求和提供的数据进行了分析,并以图表和表格的形式显示。该研究涵盖了4,682份技术投诉通知和671例不良事件。在研究期间,通知的数量逐渐增加。至于技术投诉的类型,大多数是指“可疑的质量缺陷”,最大的原因是由于“在手术过程中导管破裂”。 。最明显的不良事件是“导管破裂并迁移到身体的另一部分”。在所研究的时期内,有四次死亡通知,这是最严重的不良事件。这项研究使可视化血管导管售后监视的重要性成为可能,并提供了其使用的广泛概述。提供此概述可以支持技术监视活动,并可以作为与此产品有关的公共政策的输入。

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