Page 69 - Health Literacy, eHealth, and Communication: Putting the Consumer First: Workshop Summary
P. 69

Health Literacy, eHealth, and Communication: Putting the Consumer First: Workshop Summary


                                HeALtH LiteRACY, eHeALtH, AnD CoMMUniCAtion

                   A uSER-CENTERED PERSONAL HEALTH RECORD:
                         THE DESIgN AND DEVELOPMENT OF
                               THE SHARED CARE PLAN
                                  Dawn Gauthier, M.i.S.
                            Web Usability Designer, PeaceHealth


               In 2001 the Robert Wood Johnson Foundation awarded a Pursuing
            Perfection grant to Whatcom County, Washington (the only community
            to receive such a grant) to implement a chronic disease model, including
            the development of a user-centered personal health record (PHR). The
            project  was  also  supported  by  a  patient  safety  grant  from  the Agency
            for Healthcare Research and Quality. With the publication of Crossing the
            Quality Chasm (IOM, 2001), those working on the project kept in mind the
            report’s six aims for improvement  and the ten rules  for the health care
                                                           5
                                          4
            system as design work proceeded.
               Whatcom  County  had  been  very  much  interested  in  designing  a
            patient-centered  health  care  system.  Development  of  a  user-centered
            electronic health record, the Shared Care Plan, fit well with the activities
            of the County. The project began with a focus on chronic conditions and
            the  design  of  a  chronic-disease-management  tool.  The  involvement  of
            patients pushed the design in the direction of a personal health record.
               The design goals of the Shared Care Plan, which was an endeavor of
            the entire community including all the providers, were to
               •   facilitate  patients’  interactions  with  the  health  care  system,  sup-
                  porting the virtual Care Team concept, and planned care, and to
                  ensure  the  “nothing  about  me  without  me”  perspective  of  the
                  patient;
               •   offer patients a tool that fosters a sense of responsibility for their
                  own health and encourages them to learn about and practice prin-
                  ciples of self-management (such as maintaining a medication list),
                  thereby encouraging educated and engaged patients;
               •   provide a tool that enables patients to feel safer because they are
                  informed and in control; and


             4   The six aims for improvement for the health care system are that the system must be safe,
            effective, patient-centered, timely, efficient, and equitable (IOM, 2001).
             5   The 10 rules for the health care system are that care should be based on continuous
            healing relationships, there should be customization based on patient needs and values, the
            patient should be the source of control, there should be shared knowledge and the free flow
            of information, there should be evidence-based decision making, safety should be a system
            property, there is a need for transparency, the health system should anticipate patient needs,
            there should be a continuous decrease in waste, and there should be cooperation among
            clinicians (IOM, 2001).





                 Copyright National Academy of Sciences. All rights reserved.
   64   65   66   67   68   69   70   71   72   73   74