# 162 Advance Care Planning in Chronic Illness

FAST FACTS AND CONCEPTS #162 PDF


Author(s): Sara N Davison MD

Background   A cornerstone of excellent medical care is helping patients decide how future medical interventions match their personal goals and values for care near the end-of-life. This Fast Fact reviews key concepts of the Advance Care Planning (ACP) process.

Advance Care Planning is a process of communication between the patient, the family/health care proxy, and staff for the purpose of prospectively identifying a surrogate, clarifying treatment preferences, and developing individualized goals of care near the end of life. Advance Directives (e.g. living wills, durable powers of attorney for health care) are legal documents with capabilities and requirements that vary between jurisdictions.

Primary Goals of ACP

  • Enhance patient and family education about their illness, including prognosis and likely outcomes of alternative care plans.
  • Define the key priorities in end-of-life care and develop a care plan that addresses these issues.
  • Shape future clinical care to fit the patient's preferences and values.

Other Potential Benefits of the ACP process

  • Help patients find hope and meaning in life, and help them achieve a sense of spiritual peace.
  • Strengthen relationships with loved ones.

Timing   At a minimum, ACP should be considered whenever the health care provider would not be surprised if that patient died within the next 12 months.

Facilitating ACP

  • Take the lead in starting the discussion. Many patients are reluctant to initiate an ACP discussion; physicians and nurses can “open the door” to such discussions by asking, How do feel things are going? Have you given any thought to how you wish to be cared for should your illness worse?
  • Explain the rationale for ACP. Patients identify ACP as an important part of medical care if they have a clear idea of how the process will benefit them: I’d like to spend some time talking to you about the future course of your illness so that I have a clear understanding of your wishes.
  • Use good communication skills. Do not use medical jargon (e.g. ‘ventilator’); language used should be positive (I want to ensure you receive the kind of treatment you want). Use empathetic listening skills (using words, posture and appropriate touch to convey sense of caring) to help build a trusting relationship. Ensure privacy and allow sufficient time for the discussion.
  • Provide information. Patients require realistic information on prognosis and treatment options with an emphasis on how you expect their illness will impact their daily function.
  • Identify a surrogate. Patients should be encouraged to both identify a surrogate decision-maker and, most importantly, discuss their wishes with this individual. The power of the ACP discussion is the sharing of information between patient and the patient’s surrogate decision maker and other family members, and the health care team. The surrogate should have the greatest knowledge of the patient’s preferences and values. If desired, offer to facilitate a discussion between the patient and their surrogate or other family members.
  • Identify how future decision-making will occur. A patient may have specific desires for how information is shared among family members – this needs to be explicitly discussed.
  • Determine goals of care. If decisions need to be made at the same time as an ACP discussion, this is an appropriate venue to establish the goals of care (see Fast Fact #16, 65).

Cautions

  • The ACP process must be sensitive to disease, gender, age, social and cultural contexts.
  • Providing opportunities to discuss end-of-life issues does not mean everyone will want or be able to do so at that moment. ACP is an evolving process that requires varying amounts of time to be effective. Patients often need time to reflect on information and how it impacts their lives.

References

  1. Martin DK, Thiel EC, Singer PA. A new model of advance care planning. Observations from people with HIV. Arch Intern Med. 1999; 159: 86-92.
  2. Briggs L. Shifting the focus of advance care planning: using an in-depth interview to build and strengthen relationships. Innovations in End-of-Life Care. 2003; 5(2). Available at: http://www2.edc.org/lastacts/archives/archivesMarch03/default.asp.
  3. Johnstone SC, Pfeifer MP, McNutt R. The discussion about advance directives. Arch Intern Med. 1995; 155:1025-1030.

Fast Facts and Concepts are edited by Drew A Rosielle MD, Palliative Care Center, Medical College of Wisconsin. For more information write to: drosiell@mcw.edu. More information, as well as the complete set of Fast Facts, are available at EPERC: www.eperc.mcw.edu.

Version History: This Fast Fact was originally edited by David E Weissman MD and published in September 2006. Current version re-copy-edited in April 2009.

Copyright/Referencing Information: Users are free to download and distribute Fast Facts for educational purposes only. Davison S. Advance Care Planning in Chronic Illness. Fast Facts and Concepts. September 2006; 162. Available at: http://www.eperc.mcw.edu/EPERC/FastFactsIndex/ff_162.htm.

Disclaimer: Fast Facts and Concepts provide educational information. This information is not medical advice. Health care providers should exercise their own independent clinical judgment. Some Fast Facts cite the use of a product in a dosage, for an indication, or in a manner other than that recommended in the product labeling. Accordingly, the official prescribing information should be consulted before any such product is used.

ACGME Competencies: Patient Care, Professionalism, Systems-based practice; Interpersonal and Communication Skills

Keyword(s): Communication, Ethics, Law, Policy Health Systems