The document discusses P2I Care, a research network that aims to improve healthcare by focusing on the individual patient, provider, and health information. It describes how patient-reported outcomes captured in quality registries can empower patients and benefit both patients and providers. Quality registries in Sweden collect patient-reported data on pain levels, joint swelling, daily functioning, and more over time. This data gives patients insight into their condition and treatment and allows for shared decision making between patients and providers.