Abstract
An understanding of the tenets of medical ethics and related fundamentals of medical decision making and communication is critical to the optimal implantation, maintenance, and discontinuation of long-term mechanical circulatory support (MCS). Shared decision making incorporates the perspective of the patient, who is responsible for articulating values, goals, and preferences as they relate to his or her healthcare. For patients with advanced heart failure who are considering the option of MCS, understanding benefits, risks, burdens of available options, and outcomes (survival and health-related quality of life [HRQOL]) and changes in lifestyle, implications for caregivers, and potential for withdrawal of MCS are critical to successful implantation, within the context of patient values, preferences, and goals. An ethical process fully engages patients, their families, and the advanced heart failure team and supports the potential for successful decision making and enhanced outcomes. The purpose of this chapter is to discuss decision making and informed consent, psychosocial and behavioral evaluation prior to surgery, HRQOL outcomes, caregiver burden, and palliative care/end-of-life care for patients who undergo long-term MCS implantation.
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Abbreviations
- BTT:
-
Bridge to transplant
- DT:
-
Destination therapy
- HRQOL:
-
Health-related quality of life
- INTERMACS:
-
Interagency Registry for Mechanically Assisted Circulatory Support
- MCS:
-
Mechanical circulatory support
- NYHA:
-
New York Heart Association
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Grady, K.L., Allen, L.A., Goetz, P.W. (2017). Psychosocial Considerations of Mechanical Circulatory Support: Decision Making, Behavioral Evaluation, Quality of Life, Caregivers, and End of Life. In: Montalto, A., Loforte, A., Musumeci, F., Krabatsch, T., Slaughter, M. (eds) Mechanical Circulatory Support in End-Stage Heart Failure. Springer, Cham. https://doi.org/10.1007/978-3-319-43383-7_45
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