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Engaging Patients in New
Care Delivery Models Using
                 Health IT



                 June 27, 2011
Overview


» National Partnership for Women &
  Families
» Defining “Patient Centered Care”
» Translating What Patient Centered Care
  means for Health IT
The National Partnership

» Nonprofit organization with 40 years of experience working on
  issues important to women and families.
    ~ National level, as well as in states and communities

» Priorities:
    ~ Improve access to quality, affordable health care
    ~ Promote fairness in the workplace
    ~ Advance policies that help women and men meet the dual demands of
      work and family

» Leads the Consumer Partnership for e-Health, a diverse coalition of
  consumer groups which has been working since 2005 to ensure that efforts
  to drive health IT adoption meet the needs of patients and their families.
Definitions

» Institute of Medicine
     • Care that is respectful of and responsive to
       individual patient preferences, needs and values,
       and ensuring that patient values guide all clinical
       decisions.
» Planetree
     • An approach to the planning, delivery and
       evaluation of care grounded in mutually beneficial
       partnerships among providers, patients and
       families. It redefines relationships in health care.
Definitions, ctd.

» Consumers & consumer orgs:
 1.   Whole person care
 2.   Coordination and communication
 3.   Patient support and empowerment
 4.   Ready access
“Whole person” care
» Patients viewed as whole person rather than
  collection of body parts

» Clinicians take time to really know and
  remember patients
   ~ Requires health IT

» Clinicians understand the full range of factors
  affecting a patient’s ability to get and stay well

» Treatment recommendations align with
  patients’ values, life circumstances, preferences
Coordination and
                               communication
» Providers organized in teams
» A “go-to” person to navigate system, and help patients
  understand their condition and what they need to do
» Help choosing specialists and getting appointments in a
  timely manner
» Ensuring other providers have patient’s information ahead of
  time
   ~ Health information exchange

» Help patients understand results recommendations
» Smooth transitions between settings
   ~ Visit summary, summary record, care planning, med rec, etc
Patient support and
                        empowerment
» Expanding patients’ and caregivers’ capacity to get
  and stay well (efficacy)
» Support for self-management - tools and services
  that help patients and caregivers better manage their
  conditions
» Patient partnership with clinicians – choosing
  treatment options, goals, plans, team members, etc.

» Trust and respect – patient preferences, physical
  and emotional comfort, and privacy
Ready access

» Expand access beyond 5 minute phone call or 7
  minute office visit
   ~ eVisits, secure messaging, tele-medicine, etc.
» Getting appointments promptly

» Keeping wait times brief; and having care team
  members available when needed

» Accommodating limited physical mobility, cognitive
  impairment, language barriers, or cultural differences
Translating Patient-Centered
                Care to Health IT
» Clinical information and information contributed by the
  individual is used to provide holistic care.
» The right information is provided to the right person at
  the right time to ensure safety and quality.
» Information is used to ensure that all people are treated
  fairly and equitably by our health care system.
» Information is presented and used in ways that are
  meaningful to the individual.
Translating Patient-Centered
                Care to Health IT
» Information is available and shared in real time to
  increase accessibility, efficiency and affordability of care.
» Information is exchanged privately and securely, without
  erecting unnecessary barriers to its use.
» Communication of information results in seamless
  attention to health needs, regardless of an individual’s
  physical location.
Health IT and New Models:
                   Consumer Roles
» Agents of Change

» Informed Decision Makers
» Sources of Verification and Contextual
  Information

» Integrators of Health into Daily Lives
Source: Consumer Platform for eHealth, 2011.
  www.nationalpartnership.org/hit
Thank you!



Christine Bechtel
Vice President
202.986.2600
NationalPartnership.org

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An Overview of Principles and Strategies for Engaging Patients in New Delivery Models Using Health IT

  • 1. Engaging Patients in New Care Delivery Models Using Health IT June 27, 2011
  • 2. Overview » National Partnership for Women & Families » Defining “Patient Centered Care” » Translating What Patient Centered Care means for Health IT
  • 3. The National Partnership » Nonprofit organization with 40 years of experience working on issues important to women and families. ~ National level, as well as in states and communities » Priorities: ~ Improve access to quality, affordable health care ~ Promote fairness in the workplace ~ Advance policies that help women and men meet the dual demands of work and family » Leads the Consumer Partnership for e-Health, a diverse coalition of consumer groups which has been working since 2005 to ensure that efforts to drive health IT adoption meet the needs of patients and their families.
  • 4. Definitions » Institute of Medicine • Care that is respectful of and responsive to individual patient preferences, needs and values, and ensuring that patient values guide all clinical decisions. » Planetree • An approach to the planning, delivery and evaluation of care grounded in mutually beneficial partnerships among providers, patients and families. It redefines relationships in health care.
  • 5. Definitions, ctd. » Consumers & consumer orgs: 1. Whole person care 2. Coordination and communication 3. Patient support and empowerment 4. Ready access
  • 6. “Whole person” care » Patients viewed as whole person rather than collection of body parts » Clinicians take time to really know and remember patients ~ Requires health IT » Clinicians understand the full range of factors affecting a patient’s ability to get and stay well » Treatment recommendations align with patients’ values, life circumstances, preferences
  • 7. Coordination and communication » Providers organized in teams » A “go-to” person to navigate system, and help patients understand their condition and what they need to do » Help choosing specialists and getting appointments in a timely manner » Ensuring other providers have patient’s information ahead of time ~ Health information exchange » Help patients understand results recommendations » Smooth transitions between settings ~ Visit summary, summary record, care planning, med rec, etc
  • 8. Patient support and empowerment » Expanding patients’ and caregivers’ capacity to get and stay well (efficacy) » Support for self-management - tools and services that help patients and caregivers better manage their conditions » Patient partnership with clinicians – choosing treatment options, goals, plans, team members, etc. » Trust and respect – patient preferences, physical and emotional comfort, and privacy
  • 9. Ready access » Expand access beyond 5 minute phone call or 7 minute office visit ~ eVisits, secure messaging, tele-medicine, etc. » Getting appointments promptly » Keeping wait times brief; and having care team members available when needed » Accommodating limited physical mobility, cognitive impairment, language barriers, or cultural differences
  • 10. Translating Patient-Centered Care to Health IT » Clinical information and information contributed by the individual is used to provide holistic care. » The right information is provided to the right person at the right time to ensure safety and quality. » Information is used to ensure that all people are treated fairly and equitably by our health care system. » Information is presented and used in ways that are meaningful to the individual.
  • 11. Translating Patient-Centered Care to Health IT » Information is available and shared in real time to increase accessibility, efficiency and affordability of care. » Information is exchanged privately and securely, without erecting unnecessary barriers to its use. » Communication of information results in seamless attention to health needs, regardless of an individual’s physical location.
  • 12. Health IT and New Models: Consumer Roles » Agents of Change » Informed Decision Makers » Sources of Verification and Contextual Information » Integrators of Health into Daily Lives Source: Consumer Platform for eHealth, 2011. www.nationalpartnership.org/hit
  • 13. Thank you! Christine Bechtel Vice President 202.986.2600 NationalPartnership.org