Using the Experiences of Bereaved Caregivers to Inform Patient- and Caregiver-centered Advance Care Planning |
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Authors: | Terri R Fried John R O’Leary |
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Institution: | (1) Department of Medicine, Yale University School of Medicine, New Haven, CT, USA;(2) Clinical Epidemiology Research Center, VA Connecticut Healthcare System, West Haven, CT, USA;(3) Program on Aging, Yale University School of Medicine, New Haven, CT, USA |
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Abstract: | Background Traditional approaches to advance care planning (ACP) have many limitations; new approaches are being developed with the goal
of improving end-of-life care.
Objective To understand how the end-of-life care experiences of older patients and their caregivers can inform the development of new
approaches to ACP.
Design Qualitative cross-sectional study.
Participants Caregivers of community-dwelling persons age ≥ 60 years who died with advanced cancer, chronic obstructive pulmonary disease,
or heart failure during follow-up in a longitudinal study.
Approach In-depth interviews were conducted 6 months after the patient’s death with 64 caregivers. Interviews began with open-ended
questions to encourage the caregiver to tell the story of the patient’s experiences at the end of life. Additional questions
asked about how decisions were made, patient–caregiver, patient–clinician, and caregiver–clinician communication.
Main Results Although the experiences recounted by caregivers were highly individual, several common themes emerged from the interviews.
These included the following: 1) the lack of availability of treatment options for certain patients, prompting patients and
caregivers to consider broader end-of-life issues, 2) changes in preferences at the very end of an illness, 3) variability
in patient and caregiver desire for and readiness to hear information about the patient’s illness, and 4) difficulties with
patient–caregiver communication.
Discussion The experiences of older patients at the end of life and their caregivers support a form of ACP that includes a broader set
of issues than treatment decision-making alone, recognizes the dynamic nature of preferences, and focuses on addressing barriers
to patient–caregiver communication.
Presented at the 2006 annual meeting of the American Geriatrics Society. Supported by grant PCC 02–192 from VA HSR&D, R01
AG19769 from the National Institute on Aging, and a Paul Beeson Physician Faculty Scholars Award. Dr. Fried is supported by
K24 AG28443from the National Institute on Aging. |
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Keywords: | end-of-life care caregivers advance care planning |
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