EP 1: Coordinated Research Network
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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
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