Randomisierte kontrollierte Studien und Real-World-Evidence in der Marktzulassung und Überwachung von Hochrisikoprodukten – Das Beispiel Paclitaxel

  • C. A. Behrendt
  • U. Rother
  • G. Rümenapf
  • C. Uhl
  • H. Görtz
  • D. Böckler
  • Kommission PAVK und Diabetischer Fuß der DGG e. V.

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Abstract

In 2018 and 2020, two meta-analyses using summary-level data from randomized controlled trials reported worse mortality following the application of paclitaxel-coated stents and balloons in femoropopliteal and crural arteries. These results initiated a heated global discussion concerning the validity of this association, while various observational studies using clinical and administrative registries proved the safety of coated devices. This article aimed to summarize the development and adoption of paclitaxel-coated balloons and stents for the treatment of peripheral arterial occlusive disease in clinical practice, research, and practice guidelines. It especially focusses on the European Unionʼs medical device regulation, which has far-reaching implications for the market approval and monitoring of high-risk medical devices.

Bibliographical data

Translated title of the contributionRandomized controlled trials and real-world evidence for the market access and surveillance of high-risk products—the example of paclitaxel
Original languageGerman
ISSN0948-7034
DOIs
Publication statusPublished - 01.03.2021