How do you plan to handle patient education and disclosure around therapies that may be emerging or lack strong consensus? How is it being done now?

They provide patients with educational materials related to the therapy, provide them with the list of qualifiers that make them a potential fit for the therapy (which they said they do on a very conservative basis – ie. not making any treatment claims), and allow patients to make their own decisions about the treatment after having the opportunity to review the research and discuss with their provider.