Bereaved Caregiver Perspectives on the End-of-Life Experience of Patients With a Left Ventricular Assist Device
Author(s) -
Colleen K. McIlvennan,
J. K. N. Jones,
Larry A. Allen,
Keith M. Swetz,
Carolyn T. Nowels,
Daniel D. Matlock
Publication year - 2016
Publication title -
jama internal medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.14
H-Index - 342
eISSN - 2168-6114
pISSN - 2168-6106
DOI - 10.1001/jamainternmed.2015.8528
Subject(s) - medicine , end of life care , feeling , ventricular assist device , palliative care , confusion , advance care planning , heart failure , nursing , psychology , social psychology , psychoanalysis
For patients and their loved ones, decisions regarding the end of life in the setting of chronic progressive illness are among the most complex in health care. Complicating these decisions are increasingly available, invasive, and potentially life-prolonging technologies such as the left ventricular assist device (LVAD).
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