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
Authors
Reidy, JenniferHalvorson, Jennifer
Makowski, Suzana
Katz, Delila
Weinstein, Barbara
McCluskey, Christine
Doering, Alex
DeCarli, Kathryn
Tjia, Jennifer
UMass Chan Affiliations
School of MedicineUMass 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 ArticlePublication Date
2017-04-01Keywords
advance directiveshealth services research
physician patient communication
Health Services Administration
Health Services Research
Palliative Care
Metadata
Show full item recordAbstract
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 siteDOI
10.1089/jpm.2016.0272Permanent Link to this Item
http://hdl.handle.net/20.500.14038/29095PubMed ID
27983894Notes
Kathryn DeCarli is a medical student at UMass Medical School.
Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1089/jpm.2016.0272