The coordinated registry network (CRN) aims to collect and compare data from diverse registries with similar data points, to help physicians address specific questions based on collective real-world data.
Steve Elias meets with Jens Eldruip-Jorgensen (Maine, US), Marlin Schul (Indiana , US) and Nicholas Osbourne (Michigan, US) to find out more about the aims of the Coordinated Research Network and its impact on real-world practice to treat patients with venous disease. Highlights include discussions around the benefits and challenges of registry data, as well as a look at the current data coming out from the CRN and its implications for clinicians.
Submit your question to Steve via: podcast@radciffe-group.com.
Hosted by [inert Steve Twitter]. Produced by @RadcliffeVASCU.
What to listen for:
In this episode they discuss:
• [00.00] Introductions
• [02.40] The AVLS registry
• [04.00] The SVS registry
• [05.02] The Varicose vein registry
• [09.20] The COVER group (Consortium of venous registries)
• [11.00] Data Management and volume
• [14.23] What are the challenges?
• [16.30] The National Evaluation for Healthcare Technology (NEST) and Registry Assessment of Peripheral Interventional Devices (RAPID)
• [18.12] Involvement and input: industry, FDA and others
• [24.01] How the data can be used to benefit patient outcomes and industry
• [26.00] The value of registry participation
• [28.05] Closing remarks
