Data Review and Reporting Committee
The Data Review and Reporting Committee examines the I-MPACT data registry, and the associated data analyses and reporting strategies, to optimize the data collection and reporting process. In addition, the committee determines how I-MPACT data is best used to make collaborative wide improvements to transition of care practices.
I-MPACT works with participants and other potential authors to disseminate findings from I-MPACT data through publication of abstracts, manuscripts, presentations, and posters. If you would like to learn more about using I-MPACT data for dissemination outside of the collaborative, or have any other questions, please email email@example.com. If you already have a concept or manuscript draft, please fill out the Request for Publication Review Form.
Materials for Publication Development
The purpose of the Steering Committee is to provide general oversight and input into the I-MPACT CQI by: providing guidance regarding I-MPACT project goals and interventions; reviewing output/feedback from Data Review and Data Publication Committees; assisting with identifying best practices and implementation; providing input into P4P index goals and measures; ensuring I-MPACT maintains strong collaborative partnerships with other BCBSM CQI’s; providing input into format and structure of collaborative-wide meetings and calls.
Patient & Caregiver Advisory Group
I-MPACT has a small group of patients and caregivers who participate as e-Advisors to the initiative. Our e-Advisors are a resource used to keep the patient's voice included in I-MPACT's activities. The collaborative's goal includes a focus on patient input and these volunteer advisors help provide patient insight in our initiative.