• J Palliat Med · Dec 2011

    Giving voice to patients' and family caregivers' needs in chronic heart failure: implications for palliative care programs.

    • David B Bekelman, Carolyn T Nowels, Jessica H Retrum, Larry A Allen, Simon Shakar, Evelyn Hutt, Theresa Heyborne, Deborah S Main, and Jean S Kutner.
    • Research and Genetics Sections, Department of Veterans Affairs Medical Center, Denver, Colorado, USA. david.bekelman@va.gov
    • J Palliat Med. 2011 Dec 1; 14 (12): 131713241317-24.

    BackgroundThe American College of Cardiology Foundation/American Heart Association (ACC/AHA) Guidelines for the Management of Heart Failure recommend palliative care in the context of Stage D HF or at the end of life. Previous studies related to heart failure (HF) palliative care provide useful information about patients' experiences, but they do not provide concrete guidance for what palliative care needs are most important and how a palliative care program should be structured.ObjectivesDescribe HF patients' and their family caregivers' major concerns and needs. Explore whether, how, and when palliative care would be useful to them.Design And ParticipantsQualitative study using in-depth interviews of 33 adult outpatients with symptomatic HF identified using purposive sampling and 20 of their family caregivers.ApproachInterviews were transcribed verbatim and analyzed using the constant comparative method.Key ResultsOverall, patients and caregivers desired early support adjusting to the limitations and future course of illness, relief of a number of diverse symptoms, and the involvement of family caregivers using a team approach. A diverse group of participants desired these elements of palliative care early in illness, concurrent with their disease-specific care, coordinated by a provider who understood their heart condition and knew them well. Some diverging needs and preferences were found based on health status and age.ConclusionsHF patients and their family caregivers supported early integration of palliative care services, particularly psychosocial support and symptom control, using a collaborative team approach. Future research should test the feasibility and effectiveness of integrating such a program into routine HF care.

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