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    Health System Advance Care Planning Culture Change for High-Risk Patients: The Promise and Challenges of Engaging Providers, Patients, and Families in Systematic Advance Care Planning

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    Authors
    Reidy, Jennifer
    Halvorson, Jennifer
    Makowski, Suzana
    Katz, Delila
    Weinstein, Barbara
    McCluskey, Christine
    Doering, Alex
    DeCarli, Kathryn
    Tjia, Jennifer
    UMass Chan Affiliations
    School of Medicine
    UMass Memorial Health Care
    Center for Health Policy and Research, Commonwealth Medicine
    Department of Medicine, Division of Palliative Care
    Department of Quantitative Health Sciences
    Department of Family Medicine and Community Health
    Document Type
    Journal Article
    Publication Date
    2017-04-01
    Keywords
    advance directives
    health services research
    physician patient communication
    Health Services Administration
    Health Services Research
    Palliative Care
    
    Metadata
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    Link to Full Text
    https://doi.org/10.1089/jpm.2016.0272
    Abstract
    BACKGROUND: The success of a facilitator-based model for advance care planning (ACP) in LaCrosse, Wisconsin, has inspired health systems to aim for widespread documentation of advance directives, but limited resources impair efforts to replicate this model. One promising strategy is the development of interactive, Internet-based tools that might increase access to individualized ACP at minimal cost. However, widespread adoption and implementation of Internet-based ACP efforts has yet to be described. OBJECTIVE: We describe our early experiences in building a systematic, population-based ACP initiative focused on health system-wide deployment of an Internet-based tool as an adjunct to a facilitator-based model. METHODS: With the sponsorship of our healthcare system's population health leadership, we engaged a diverse group of clinical stakeholders as champions to design an Internet-based ACP tool and facilitate local practice change. We describe how we simultaneously began to train clinicians in ACP conversations, engage patients and health system employees in thinking about ACP, redesign clinic workflows to accommodate ACP discussions, and integrate the Internet-based tool into the electronic medical record (EMR). RESULTS: Over 18 months, our project engaged two subspecialty clinics in a systematic ACP process and began work with a large primary care practice with a large Medicare Accountable Care Organization at-risk population. Overall, 807 people registered at the Internet site and 85% completed ACPs. CONCLUSION: We learned that changing culture and systems to promote ACP requires a comprehensive vision with simultaneous, interconnected strategies targeting patient education, clinician training, EMR documentation, and community awareness.
    Source
    J Palliat Med. 2017 Apr;20(4):388-394. Epub 2016 Dec 16. Link to article on publisher's site
    DOI
    10.1089/jpm.2016.0272
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/29095
    PubMed ID
    27983894
    Notes

    Kathryn DeCarli is a medical student at UMass Medical School.

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    Link to Article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1089/jpm.2016.0272
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