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PATIENT- CENTERED CARE: BOTH IN INDIVIDUAL CONVERSATIONS WITH PATIENTS AND IN PRACTICE TRANSFORMATION EFFORTS Integrated Network Engagement Summit 9/21/17 Aimee English, MD

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  • PATIENT-

    CENTERED

    CARE:

    BOTH IN INDIVIDUAL CONVERSATIONS

    WITH PATIENTS AND IN PRACTICE

    TRANSFORMATION EFFORTS

    Integrated Network Engagement Summit

    9/21/17

    Aimee English, MD

  • OVERVIEW

    • Engaging patients and families in direct care

    • Background

    • Shared decision making tools

    • Action Plans

    • Program Requirements

    • Engaging patients and families in practice transformation

    • Background

    • Various Methods

    • Tips for Success

    • Support Materials

    • Program Requirements

  • INDIVIDUAL PATIENT

    ENGAGEMENT

  • WHO MANAGES

    CHRONIC DISEASE?

    Providers

    Case Managers

    Social Workers

    NursesPatient Themself

    Spouses

    Personal Care Givers

    Siblings

    Parents

    Friends

  • RISING RATES OF

    CHRONIC ILLNESS

    Medical Expenditure Panel Survey 2006.

    Wu, Shin-Yi, and Green, Anthony. Projection

    of Chronic Illness Prevalence and Cost

    Inflation.RAND Corporation, October 2000

  • STAGES OF ACTIVATION

    Stage 1:

    Beliefs about the

    importance of the

    patient role

    Stage 2:

    Knowledge and

    confidence

    necessary to take

    action

    Stage 3:

    Actually taking

    action

    Stage 4:

    Staying the course

    under stressHibbard J, Stockard J, Mahoney E, and Tusler M. Development of the Patient Activation Measur (PAM): Conceptualizing and Measuring Activation in Patients and Consumers. Health Sciences

    Research. 2004; 39(4): 1005 - 1026.

    More likely to:

    Adhere to treatment regimens, get preventive care,

    participate more in decisions about their care, engage in

    healthy behaviors, seek out and use health information,

    when controlling for health status, gender, age, and

    income level.

    Hibbard J, Greene J, and Overton V. Patients with Lower Activation Associated with Higher Costs; Delivery System Should Know Their Patients’ ‘Scores.’ Health Affairs. 2013. 32(2): 216-222.

    More likely to:

    Use EDs, be hospitalized, have

    higher costs of care, have poorer

    health outcomes across a variety of

    diseases, have unmet medical needs

    and delay care.

  • EXAMPLES OF SELF-

    MANAGEMENT

    EDUCATION/SUPPORT

    • Goal-setting action plans

    • Interactive Patient Education

    • Motivational Interviewing

    • Shared care plans (with collaborative goalsetting)

    • Shared Decision Aids

    • Tracking tools –journaling, My Fitness Pal, Mood Tracker

    • Self-triage tools

  • COCHRANE REVIEW:

    DECISION AIDS

    Decision Aids for People Facing

    Health Treatment or Screening Decision.

    (N= 105 studies including 31,043 participants)

    Results:

    • increased knowledge (MD 13.27/100; 95% CI 11.32-15.23)

    • improved accurate perception of risks (RR 2.10, 95% CI 1.66-2.66)

    • lower decisional conflict d/t feeling uninformed (MD -9.28/100 95% CI -12.20 to

    -6.36)

    • reduced proportion of people who were passive in decision making (RR 0.68;

    95% CI 0.55 to 0.83)

    • unknown effect on visit time – 2.6 minutes longer (24 vs. 21 min)

    Stacey D, et al. Decision aids for people facing health treatment or screening decisions. Cochrane Database of Systematic Reviews. 12 Apr 2017.

  • DECISION AIDS

    Ottawa Hospital Research Institute:

    • https://decisionaid.ohri.ca/AZlist.html

    Mayo:

    • http://shareddecisions.mayoclinic.org/decision-aid-

    information/decision-aids-for-chronic-disease/

    AHRQ

    • http://effectivehealthcare.ahrq.gov/index.cfm/tools-and-

    resources/patient-decision-aids/

    Stacey D, Légaré F, Col NF, Bennett CL, Barry MJ, Eden KB, Holmes-Rovner M, Llewellyn-Thomas H, Lyddiatt A, Thomson R, Trevena L, Wu JHC. Decision

    aids for people facing health treatment or screening decisions. Cochrane Database of Systematic Reviews 2014, Issue 1. Art. No.: CD001431. DOI:

    10.1002/14651858.CD001431.pub4.

    https://decisionaid.ohri.ca/AZlist.htmlhttp://shareddecisions.mayoclinic.org/decision-aid-information/decision-aids-for-chronic-disease/http://effectivehealthcare.ahrq.gov/index.cfm/tools-and-resources/patient-decision-aids/

  • ACTION PLANS

    Coleman M. Supporting Self-Management in Patients with Chronic Illness. American Family Physician. 2005. 72 (8); 1503 – 1510.

  • ACTION PLANS

  • SIM REQUIREMENTS

    SIM:

    • Implement shared decision making tools or aids in two health

    conditions, decisions or tests as component of shared decision-

    making, one of which in primary care must be related to BH and in

    CMHC must be related to physical health.

    • Track use of shared decision making aids using one of the following

    methods:

    1. A metric tracking the proportion of patients and families

    eligible for the decision aid who receive the decision aid; OR

    2. Quarterly counts of patients and families receiving individual

    aids.

    SIM Milestones. 2016.

  • 2017 NCQA

    REQUIREMENTS

    Knowing and Managing Your Patients, Competency F,

    22:

    Provides access to educational resources, such as

    materials, peer support sessions, group classes, online

    self-management tools or programs (1 credit)

    Knowing and Managing Your Patients, Competency F,

    24:

    Adopts shared decision-making aids for preference-

    sensitive conditions (1 credit)

  • CPC+ TRACK 1

    REQUIREMENT

    4.2 Assess practice capability and plan for support of

    patients’ self-management.

  • ENGAGING PATIENTS AND

    FAMILIES IN PRACTICE

    TRANSFORMATION

  • BACKGROUND

  • BACKGROUND

    When patients assist in selecting quality improvement topics the

    choices they make are more aligned with core components of the

    Chronic Care Model. Time to reach consensus is only minimally

    increased (by 10%).

    Boivin, A.; Lehoux, P.; Lacombe, R.; Burgers, J.; Grol, R., Implement Sci 2014, 9.

  • METHODS OF ENGAGING

    PATIENTS & FAMILIES OR

    GETTING FEEDBACK

    PFAC

    QI TeamsLeadership Mtgs

    One-time Focus

    Groups Waiting Room Rounds

    Group Concept

    Mapping

    Experience

    Surveys

    LaNoue M, et al. Concept Mapping as a Method to Engage Patients in Clinical Quality Improvement. Ann Fam Med. 2016, 14(2): 370 – 376.

  • METHODS OF ENGAGING

    PATIENTS & FAMILIES OR

    GETTING FEEDBACK

    PFAC

    QI TeamsLeadership Mtgs

    Focus Groups

    Waiting Room Rounds

    Group Concept

    Mapping

    Experience

    Surveys

    ?

  • ENGAGING PATIENTS IN PRACTICE

    TRANSFORMATION:

    TIPS FOR SUCCESS

    Recruit Thoughtfully

    • Methods

    • The “right” patient

    • Meeting times

    selection

    • Seek representation

    • Define advisor

    roles/mission upfront

  • Have a clear mission that’s well understood by leadership, clinic

    members, and advisors.

    ENGAGING PATIENTS IN PRACTICE

    TRANSFORMATION:

    TIPS FOR SUCCESS

  • Ask patient

    advisors for

    feedback?

    Engage patients early in an intervention.

    ENGAGING PATIENTS IN PRACTICE

    TRANSFORMATION:

    TIPS FOR SUCCESS

  • Ask patient

    advisors for

    feedback?

    Otherwise, they might feel tokenistic or that their advice won’t matter.

    ENGAGING PATIENTS IN PRACTICE

    TRANSFORMATION:

    TIPS FOR SUCCESS

  • SIM REQUIREMENTS

    SIM:

    • Assess and improve patient and family experience of care by

    selecting at least one of the following:

    • Regular patient and family surveys at least quarterly

    • Patient and family advisory council that meets at least quarterly.

    • Develop communication(s) to patients, families, and the clinic about

    the specific changes the practice is implementing, including

    efforts…as a result of, or influenced by, your practice survey/PFAC

    activities.

    SIM Milestones. 2016.

  • 2017 NCQA

    REQUIREMENT

    Team Based Care and Practice Organization,

    Competency A, 04:

    Patients/families/caregivers are involved in the practice’s

    governance structure or on stakeholder committees (2

    credits)

  • CPC+ TRACK 1

    REQUIREMENT

    4.1 Convene a PFAC (patient family advisory council) at

    least once in PY2017, and integrate recommendations

    into care, as appropriate

  • QUESTIONS?/

    COMMENTS?

    [email protected]