The National Health Council (NHC) and its partners have undertaken a process to create a Blueprint for developing patient-centered core impact sets, or PC-CIS, to address inconsistencies between what is important to patients to the information typically collected in research and care. A PC-CIS is a patient-derived and -prioritized list of impacts a disease and/or its treatments have on a patient and his/her life as well as that of their family and caregivers.

The Dialogue meeting was intended to:

1. Support socializing the PC-CIS concept;
2. Disseminate the PC-CIS Blueprint; and
3. Capture from prospective PC-CIS Blueprint users, the strengths, and challenges they anticipate for Blueprint operationalization, and future PC-CIS development and use. 

This Dialogue is funded through a Patient-Centered Outcomes Research Institute® (PCORI®) Eugene Washington PCORI Engagement Award (EASCS-24850).